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HK1160169B - Methods and means for efficient skipping of exon 45 in duchenne muscular dystrophy pre-mrna - Google Patents

Methods and means for efficient skipping of exon 45 in duchenne muscular dystrophy pre-mrna Download PDF

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Publication number
HK1160169B
HK1160169B HK12100495.6A HK12100495A HK1160169B HK 1160169 B HK1160169 B HK 1160169B HK 12100495 A HK12100495 A HK 12100495A HK 1160169 B HK1160169 B HK 1160169B
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Prior art keywords
seq
oligonucleotide
rna
artificial
antisense oligonucleotide
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HK12100495.6A
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German (de)
French (fr)
Chinese (zh)
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HK1160169A1 (en
Inventor
Johannes De Kimpe Josephus
Johannes Platenburg Gerardus
Christina Theodora Van Deutekom Judith
Aartsma-Rus Annemieke
Boudewijn Van Ommen Garrit-Jan
Original Assignee
Biomarin Technologies B.V.
Academisch Ziekenhuis Leiden
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Priority claimed from PCT/NL2008/050673 external-priority patent/WO2009054725A2/en
Application filed by Biomarin Technologies B.V., Academisch Ziekenhuis Leiden filed Critical Biomarin Technologies B.V.
Priority claimed from PCT/NL2009/050006 external-priority patent/WO2010050801A1/en
Publication of HK1160169A1 publication Critical patent/HK1160169A1/en
Publication of HK1160169B publication Critical patent/HK1160169B/en

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Description

Field
The invention relates to the field of genetics, more specifically human genetics. The invention in particular relates to the modulation of splicing of the human Duchenne Muscular Dystrophy pre-mRNA.
Background of the invention
Myopathies are disorders that result in functional impairment of muscles. Muscular dystrophy (MD) refers to genetic diseases that are characterized by progressive weakness and degeneration of skeletal muscles. Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are the most common childhood forms of muscular dystrophy. They are recessive disorders and because the gene responsible for DMD and BMD resides on the X-chromosome, mutations mainly affect males with an incidence of about 1 in 3500 boys.
DMD and BMD are caused by genetic defects in the DMD gene encoding dystrophin, a muscle protein that is required for interactions between the cytoskeleton and the extracellular matrix to maintain muscle fiber stability during contraction. DMD is a severe, lethal neuromuscular disorder resulting in a dependency on wheelchair support before the age of 12 and DMD patients often die before the age of thirty due to respiratory-or heart failure. In contrast, BMD patients often remain ambulatory until later in life, and have near normal life expectancies. DMD mutations in the DMD gene are mainly characterized by frame shifting insertions or deletions or nonsense point mutations, resulting in the absence of functional dystrophin. BMD mutations in general keep the reading frame intact, allowing synthesis of a partly functional dystrophin.
During the last decade, specific modification of splicing in order to restore the disrupted reading frame of the DMD transcript has emerged as a promising therapy for Duchenne muscular dystrophy (DMD) (van Ommen, van Deutekom, Aartsma-Rus, Curr Opin Mol Ther. 2008;10(2):140-9, Yokota, Duddy, Partidge, Acta Myol. 2007;26(3):179-84, van Deutekom et al., N Engl J Med. 2007;357(26):2677-86).
Using antisense oligonucleotides (AONs) interfering with splicing signals the skipping of specific exons can be induced in the DMD pre-mRNA, thus restoring the open reading frame and converting the severe DMD into a milder BMD phenotype (van Deutekom et al. Hum Mol Genet. 2001; 10: 1547-54; Aartsma-Rus et al., Hum Mol Genet 2003; 12(8):907-14.). In vivo proof-of-concept was first obtained in the mdx mouse model, which is dystrophin-deficient due to a nonsense mutation in exon 23. Intramuscular and intravenous injections of AONs targeting the mutated exon 23 restored dystrophin expression for at least three months (Lu et al. Nat Med. 2003; 8: 1009-14; Lu et al., Proc Natl Acad Sci U S A. 2005;102(1):198-203). This was accompanied by restoration of dystrophin-associated proteins at the fiber membrane as well as functional improvement of the treated muscle. In vivo skipping of human exons has also been achieved in the hDMD mouse model, which contains a complete copy of the human DMD gene integrated in chromosome 5 of the mouse (Bremmer-Bout et al. Molecular Therapy. 2004; 10: 232-40; 't Hoen et al. J Biol Chem. 2008; 283: 5899-907).
As the majority of DMD patients have deletions that cluster in hotspot regions, the skipping of a small number of exons is applicable to relatively large numbers of patients. The actual applicability of exon skipping can be determined for deletions, duplications and point mutations reported in DMD mutation databases such as the Leiden DMD mutation database available at www.dmd.nl. Therapeutic skipping of exon 45 of the DMD pre-mRNA would restore the open reading frame of DMD patients having deletions including but not limited to exons 12-44, 18-44, 44, 46, 46-47, 46-48, 46-49, 46-51, 46-53, 46-55, 46-59, 46-60 of the DMD pre-mRNA, occurring in a total of 16 % of all DMD patients with a deletion (Aartsma-Rus and van Deutekom, 2007, Antisense Elements (Genetics) Research Focus, 2007 Nova Science Publishers, Inc). Furthermore, for some DMD patients the simultaneous skipping of one of more exons in addition to exon 45, such as exons 51 or 53 is required to restore the correct reading frame. None-limiting examples include patients with a deletion of exons 46-50 requiring the co-skipping of exons 45 and 51, or with a deletion of exons 46-52 requiring the co-skipping of exons 45 and 53.
Recently, a first-in-man study was successfully completed where an AON inducing the skipping of exon 51 was injected into a small area of the tibialis anterior muscle of four DMD patients. Novel dystrophin expression was observed in the majority of muscle fibers in all four patients treated, and the AON was safe and well tolerated (van Deutekom et al. N Engl J Med. 2007; 357: 2677-86).
Most AONs studied contain up to 20 nucleotides, and it has been argued that this relatively short size improves the tissue distribution and/or cell penetration of an AON. However, such short AONs will result in a limited specificity due to an increased risk for the presence of identical sequences elsewhere in the genome, and a limited target binding or target affinity due to a low free energy of the AON-target complex. Therefore the inventors decided to design new and optionally improved antisense oligonucleotides that would not exhibit all of these drawbacks.
WO2007/135105 discloses two antisense oligonucleotides of less than 21 nucleotides targeting a subregion of SEQ ID NO:2 of exon 45 of the dystrophin pre-mRNA.
Description of the invention Method
In a first aspect, the invention provides a method for inducing and/or promoting skipping of exon 45 of DMD pre-mRNA in a patient, preferably in an isolated cell of said patient, the method comprising providing said cell and/or said patient with an antisense oligonucleotide comprising the nucleotide sequence SEQ ID NO: 3.
Accordingly, a method is herewith provided for inducing and/or promoting skipping of exon 45 of DMD pre-mRNA, preferably in an isolated cell of a patient, the method comprising providing said cell and/or said patient with said antisense oligonucleotides.
It is to be understood that said method encompasses an in vitro, in vivo or ex vivo method.
As defined herein a DMD pre-mRNA preferably means the pre-mRNA of a DMD gene of a DMD or BMD patient. The DMD gene or protein corresponds to the dystrophin gene or protein.
A patient is preferably intended to mean a patient having DMD or BMD as later defined herein or a patient susceptible to develop DMD or BMD due to his or her genetic background.
In the disclosure, exon skipping refers to the induction in a cell of a mature mRNA that does not contain a particular exon that is normally present therein. Exon skipping is achieved by providing a cell expressing the pre-mRNA of said mRNA with a molecule capable of interfering with sequences such as, for example, the splice donor or splice acceptor sequence that are both required for allowing the enzymatic process of splicing, or a molecule that is capable of interfering with an exon inclusion signal required for recognition of a stretch of nucleotides as an exon to be included in the mRNA. The term pre-mRNA refers to a non-processed or partly processed precursor mRNA that is synthesized from a DNA template in the cell nucleus by transcription.
Within the context of the invention inducing and/or promoting skipping of an exon as indicated herein means that at least 1%, 10%, 20%, 30%, 40%,50%, 60%, 70%, 80%, 90% or more of the DMD mRNA in one or more (muscle) cells of a treated patient will not contain said exon. This is preferably assessed by PCR as described in the examples.
Preferably, a method of the invention by inducing or promoting skipping of exon 45 of the DMD pre-mRNA in one or more cells of a patient provides said patient with a functional dystrophin protein and/or decreases the production of an aberrant dystrophin protein in said patient. Therefore a preferred method is a method, wherein a patient or a cell of said patient is provided with a functional dystrophin protein and/or wherein the production of an aberrant dystrophin protein in said patient or in a cell of said patient is decreased Decreasing the production of an aberrant dystrophin may be assessed at the mRNA level and preferably means that 99%, 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10%, 5% or less of the initial amount of aberrant dystrophin mRNA, is still detectable by RT PCR. An aberrant dystrophin mRNA or protein is also referred to herein as a non-functional dystrophin mRNA or protein. A non functional dystrophin protein is preferably a dystrophin protein which is not able to bind actin and/or members of the DGC protein complex. A non-functional dystrophin protein or dystrophin mRNA does typically not have, or does not encode a dystrophin protein with an intact C-terminus of the protein.
Increasing the production of a functional dystrophin in said patient or in a cell of said patient may be assessed at the mRNA level (by RT-PCR analysis) and preferably means that a detectable amount of a functional dystrophin mRNA is detectable by RT PCR. In another embodiment, 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the detectable dystrophin mRNA is a functional dystrophin mRNA. Increasing the production of a functional dystrophin in said patient or in a cell of said patient may be assessed at the protein level (by immunofluorescence and western blot analyses) and preferably means that a detectable amount of a functional dystrophin protein is detectable by immunofluorescence or western blot analysis. In another embodiment, 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the detectable dystrophin protein is a functional dystrophin protein.
As defined herein, a functional dystrophin is preferably a wild type dystrophin corresponding to a protein having the amino acid sequence as identified in SEQ ID NO: 1. A functional dystrophin is preferably a dystrophin, which has an actin binding domain in its N terminal part (first 240 amino acids at the N terminus), a cystein-rich domain (amino acid 3361 till 3685) and a C terminal domain (last 325 amino acids at the C terminus) each of these domains being present in a wild type dystrophin as known to the skilled person. The amino acids indicated herein correspond to amino acids of the wild type dystrophin being represented by SEQ ID NO:1. In other words, a functional dystrophin is a dystrophin which exhibits at least to some extent an activity of a wild type dystrophin. "At least to some extent" preferably means at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 100% of a corresponding activity of a wild type functional dystrophin. In this context, an activity of a functional dystrophin is preferably binding to actin and to the dystrophin-associated glycoprotein complex (DGC) (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). Binding of dystrophin to actin and to the DGC complex may be visualized by either co-immunoprecipitation using total protein extracts or immunofluorescence analysis of cross-sections, from a muscle biopsy, as known to the skilled person.
Individuals or patients suffering from Duchenne muscular dystrophy typically have a mutation in the DMD gene that prevent synthesis of the complete dystrophin protein, i.e of a premature stop prevents the synthesis of the C-terminus. In Becker muscular dystrophy the DMD gene also comprises a mutation compared to the wild type gene but the mutation does typically not induce a premature stop and the C-terminus is typically synthesized. As a result a functional dystrophin protein is synthesized that has at least the same activity in kind as the wild type protein, not although not necessarily the same amount of activity. The genome of a BMD individual typically encodes a dystrophin protein comprising the N terminal part (first 240 amino acids at the N terminus), a cystein-rich domain (amino acid 3361 till 3685) and a C terminal domain (last 325 amino acids at the C terminus) but its central rod shaped domain may be shorter than the one of a wild type dystrophin (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). Exon -skipping for the treatment of DMD is typically directed to overcome a premature stop in the pre-mRNA by skipping an exon in the rod-shaped domain to correct the reading frame and allow synthesis of the remainder of the dystrophin protein including the C-terminus, albeit that the protein is somewhat smaller as a result of a smaller rod domain. In a preferred embodiment, an individual having DMD and being treated by a method as defined herein will be provided a dystrophin which exhibits at least to some extent an activity of a wild type dystrophin. More preferably, if said individual is a Duchenne patient or is suspected to be a Duchenne patient, a functional dystrophin is a dystrophin of an individual having BMD: typically said dystrophin is able to interact with both actin and the DGC, but its central rod shaped domain may be shorter than the one of a wild type dystrophin (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). The central rod-shaped domain of wild type dystrophin comprises 24 spectrin-like repeats (Aartsma-Rus A et al, (2006), Entries in the leiden Duchenne Muscular Dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule, Muscle Nerve, 34: 135-144). For example, a central rod-shaped domain of a dystrophin as provided herein may comprise 5 to 23, 10 to 22 or 12 to 18 spectrin-like repeats as long as it can bind to actin and to DGC.
A method of the invention may alleviate one or more characteristics of a muscle cell from a DMD patient comprising deletions including but not limited to exons 12-44, 18-44, 44, 46, 46-47, 46-48, 46-49, 46-51, 46-53, 46-55, 46-59, 46-60 of the DMD pre-mRNA of said patient (Aartsma-Rus and van Deutekom, 2007, Antisense Elements (Genetics) Research Focus, 2007 Nova Science Publishers, Inc) as well as from DMD patients requiring the simultaneous skipping of one of more exons in addition to exon 45 including but not limited to patients with a deletion of exons 46-50 requiring the co-skipping of exons 45 and 51, or with a deletion of exons 46-52 requiring the co-skipping of exons 45 and 53.
In a preferred method, one or more symptom(s) or characteristic(s) of a myogenic cell or muscle cell from a DMD patient is/are alleviated. Such symptoms or characteristics may be assessed at the cellular, tissue level or on the patient self.
An alleviation of one or more symptoms or characteristics may be assessed by any of the following assays on a myogenic cell or muscle cell from a patient: reduced calcium uptake by muscle cells, decreased collagen synthesis, altered morphology, altered lipid biosynthesis, decreased oxidative stress, and/or improved muscle fiber function, integrity, and/or survival. These parameters are usually assessed using immunofluorescence and/or histochemical analyses of cross sections of muscle biopsies. The improvement of muscle fiber function, integrity and/or survival may also be assessed using at least one of the following assays: a detectable decrease of creatine kinase in blood, a detectable decrease of necrosis of muscle fibers in a biopsy cross-section of a muscle suspected to be dystrophic, and/or a detectable increase of the homogeneity of the diameter of muscle fibers in a biopsy cross-section of a muscle suspected to be dystrophic. Each of these assays is known to the skilled person.
Creatine kinase may be detected in blood as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). A detectable decrease in creatine kinase may mean a decrease of 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more compared to the concentration of creatine kinase in a same DMD patient before treatment.
A detectable decrease of necrosis of muscle fibers is preferably assessed in a muscle biopsy, more preferably as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006) using biopsy cross-sections. A detectable decrease of necrosis may be a decrease of 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or more of the area wherein necrosis has been identified using biopsy cross-sections. The decrease is measured by comparison to the necrosis as assessed in a same DMD patient before treatment.
A detectable increase of the homogeneity of the diameter of muscle fibers is preferably assessed in a muscle biopsy cross-section, more preferably as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). The increase is measured by comparison to the homogeneity of the diameter of muscle fibers in a muscle biopsy cross-section of a same DMD patient before treatment.
An alleviation of one or more symptoms or characteristics may be assessed by any of the following assays on the patient self: prolongation of time to loss of walking, improvement of muscle strength, improvement of the ability to lift weight, improvement of the time taken to rise from the floor, improvement in the nine-meter walking time, improvement in the time taken for four-stairs climbing, improvement of the leg function grade, improvement of the pulmonary function, improvement of cardiac function, improvement of the quality of life. Each of these assays is known to the skilled person. As an example, the publication of Manzur at al (Manzur AY et al, (2008), Glucocorticoid corticosteroids for Duchenne muscular dystrophy (review), Wiley publishers, The Cochrane collaboration.) gives an extensive explanation of each of these assays. For each of these assays, as soon as a detectable improvement or prolongation of a parameter measured in an assay has been found, it will preferably mean that one or more symptoms of Duchenne Muscular Dystrophy has been alleviated in an individual using a method of the invention. Detectable improvement or prolongation is preferably a statistically significant improvement or prolongation as described in Hodgetts et al (Hodgetts S., et al, (2006), Neuromuscular Disorders, 16: 591-602.2006). Alternatively, the alleviation of one or more symptom(s) of Duchenne Muscular Dystrophy may be assessed by measuring an improvement of a muscle fiber function, integrity and/or survival as later defined herein.
A treatment in a method according to the invention may have a duration of at least one week, at least one month, at least several months, at least one year, at least 2, 3, 4, 5, 6 years or more. The frequency of administration of an antisense oligonucleotide, composition, compound of the invention may depend on several parameters such as the age of the patient, the type of mutation, the number of molecules (dose), the formulation of said molecule. The frequency may be ranged between at least once in a two weeks, or three weeks or four weeks or five weeks or a longer time period. Each antisense oligonucleotide or equivalent thereof as defined herein for use according to the invention may be suitable for direct administration to a cell, tissue and/or an organ in vivo of individuals affected by or at risk of developing DMD and may be administered directly in vivo, ex vivo or in vitro. An antisense oligonucleotide as used herein may be suitable for administration to a cell, tissue and/or an organ in vivo of individuals affected by or at risk of developing DMD, and may be administered in vivo, ex vivo or in vitro. Said antisense oligonucleotide may be directly or indirectly administrated to a cell, tissue and/or an organ in vivo of an individual affected by or at risk of developing DMD, and may be administered directly or indirectly in vivo, ex vivo or in vitro. As Duchenne muscular dystrophy has a pronounced phenotype in muscle cells, it is preferred that said cells are muscle cells, it is further preferred that said tissue is a muscular tissue and/or it is further preferred that said organ comprises or consists of a muscular tissue. A preferred organ is the heart. Preferably said cells comprise a gene encoding a mutant dystrophin protein. Preferably said cells are cells of an individual suffering from DMD.
An antisense oligonucleotide or equivalent thereof can be delivered as is to a cell. When administering said antisense oligonucleotide or equivalent thereof to an individual, it is preferred that it is dissolved in a solution that is compatible with the delivery method. For intravenous, subcutaneous, intramuscular, intrathecal and/or intraventricular administration it is preferred that the solution is a physiological salt solution. Particularly preferred for a method of the invention is the use of an excipient that will further enhance delivery of said antisense oligonucleotide or functional equivalent thereof as defined herein, to a cell and into a cell, preferably a muscle cell. Preferred excipient are defined in the section entitled "pharmaceutical composition". In vitro, we obtained very good results using polyethylenimine (PEI, ExGen500, MBI Fermentas), as shown in the example.
In a preferred method of the invention, an additional antisense oligonucleotide is used which is able to induce and/or promote skipping of a distinct exon of the DMD pre-mRNA of a patient. Preferably, the second exon is selected from: exon 7, 44, 46, 51, 53, 59, 67 of the dystrophin pre-mRNA of a patient. Antisense oligonucleotides which can be used are depicted in table 2. Preferred antisense oligonucleotides comprise or consist of any of the antisense oligonucleotides as disclosed in table 2. Several antisense oligonucleotides may also be used in combination.This way, inclusion of two or more exons of a DMD pre-mRNA in mRNA produced from this pre-mRNA is prevented. This embodiment is further referred to as double- or multi-exon skipping (Aartsma-Rus A, Janson AA, Kaman WE, et al. Antisense-induced multiexon skipping for Duchenne muscular dystrophy makes more sense. Am J Hum Genet 2004;74(1):83-92, Aartsma-Rus A, Kaman WE, Weij R, den Dunnen JT, van Ommen GJ, van Deutekom JC. Exploring the frontiers of therapeutic exon skipping for Duchenne muscular dystrophy by double targeting within one or multiple exons. Mol Ther 2006;14(3):401-7). In most cases double-exon skipping results in the exclusion of only the two targeted exons from the dystrophin pre-mRNA. However, in other cases it was found that the targeted exons and the entire region in between said exons in said pre-mRNA were not present in the produced mRNA even when other exons (intervening exons) were present in such region. This multi-skipping was notably so for the combination of antisense oligonucleotides derived from the DMD gene, wherein one antisense oligonucleotide for exon 45 and one antisense oligonucleotide for exon 51 was added to a cell transcribing the DMD gene. Such a set-up resulted in mRNA being produced that did not contain exons 45 to 51. Apparently, the structure of the pre-mRNA in the presence of the mentioned antisense oligonucleotides was such that the splicing machinery was stimulated to connect exons 44 and 52 to each other.
It is possible to specifically promote the skipping of also the intervening exons by providing a linkage between the two complementary antisense oligonucleotides. Hence, in one embodiment stretches of nucleotides complementary to at least two dystrophin exons are separated by a linking moiety. The at least two stretches of nucleotides are thus linked in this embodiment so as to form a single molecule.
In case, more than one compounds are used in a method of the invention, said compounds can be administered to an individual in any order. In one embodiment, said compounds are administered simultaneously (meaning that said compounds are administered within 10 hours, preferably within one hour). This is however not necessary. In another embodiment, said compounds are administered sequentially.
Antisense oligonucleotide
In a second aspect, there is provided an antisense oligonucleotide for use in a method as described in the previous section entitled "Method". Said antisense oligonucleotide is preferably an antisense oligonucleotide (AON) or antisense oligoribonucleotide.
It was found by the present investigators that especially exon 45 is specifically skipped at a high frequency using an antisense oligonucleotide comprising the nulceotide sequence SEQ ID NO: 3. Although this effect can be associated with a higher binding affinity of said molecule, compared to a molecule that binds to a continuous stretch of less than 21 nucleotides, there could be other intracellular parameters involved that favor thermodynamic, kinetic, or structural characteristics of the hybrid duplex. In the disclosure, a molecule that binds to a continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides within said exon may be used.
In the disclosure, a molecule or an oligonucleotide of the invention which comprises a sequence that is complementary to a part of exon 45 of DMD pre-mRNA is such that the complementary part is at least 50% of the length of the oligonucleotide, more preferably at least 60%, even more preferably at least 70%, even more preferably at least 80%, even more preferably at least 90% or even more preferably at least 95%, or even more preferably 98% and most preferably up to 100%. "A part of exon 45" preferably means a stretch of at least 21 nucleotides. In the disclosure, an oligonucleotide consists of a sequence that is complementary to part of exon 45 dystrophin pre-mRNA as defined herein. Alternatively, an oligonucleotide may comprise a sequence that is complementary to part of exon 45 dystrophin pre-mRNA as defined herein and additional flanking sequences. In the disclosure , the length of said complementary part of said oligonucleotide is of at least 21, 22, 23, 24, 25, 26, 27, 28 , 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50 nucleotides. Several types of flanking sequences may be used. In the disclosure, preferably additional flanking sequences are used to modify the binding of a protein to said molecule or oligonucleotide, or to modify a thermodynamic property of the oligonucleotide, more preferably to modify target RNA binding affinity. In another preferred embodiment, additional flanking sequences are complementary to sequences of the DMD pre-mRNA which are not present in exon 45. Such flanking sequences are preferably complementary to sequences comprising or consisting of the splice site acceptor or donor consensus sequences of exon 45. In a preferred embodiment, such flanking sequences are complementary to sequences comprising or consisting of sequences of an intron of the DMD pre-mRNA which is adjacent to exon 45; i.e. intron 44 or 45.
In the disclosure, a continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides within exon 45 is selected from the sequence:
It was found that a molecule that binds to a nucleotide sequence comprising or consisting of a continuous stretch of at least 21, 25, 30, 35, 40, 45, 50 nucleotides of SEQ ID NO. 2 results in highly efficient skipping of exon 45 in a cell provided with this molecule. Molecules that bind to a nucleotide sequence comprising a continuous stretch of less than 21 nucleotides of SEQ ID NO:2 were found to induce exon skipping in a less efficient way than the molecules of the disclosure. Therefore, in the disclosure, a method is provided wherein a molecule binds to a continuous stretch of at least 21, 25, 30, 35 nucleotides within SEQ ID NO:2. Contrary to what was generally thought, the inventors surprisingly found that a higher specificity and efficiency of exon skipping may be reached using an oligonucleotides having a length of at least 21 nucleotides. None of the indicated sequences is derived from conserved parts of splice-junction sites. Therefore, said molecule is not likely to mediate differential splicing of other exons from the DMD pre-mRNA or exons from other genes.
In the disclosure, a molecule of the invention capable of interfering with the inclusion of exon 45 of the DMD pre-mRNA is a compound molecule that binds to the specified sequence, or a protein such as an RNA-binding protein or a non-natural zinc-finger protein that has been modified to be able to bind to the indicated nucleotide sequence on a RNA molecule. Methods for screening compound molecules that bind specific nucleotide sequences are for example disclosed in PCT/NL01/00697 and US patent 6875736 , which are herein enclosed by reference. Methods for designing RNA-binding Zinc-finger proteins that bind specific nucleotide sequences are disclosed by Friesen and Darby, Nature Structural Biology 5: 543- 546 (1998) which is herein enclosed by reference.
In the disclosure, a molecule of the invention is capable of interfering with the inclusion of exon 45 of the DMD pre-mRNA and comprises an antisense oligonucleotide that is complementary to and can base-pair with the coding strand of the pre-mRNA of the DMD gene. Said antisense oligonucleotide preferably contains a RNA residue, a DNA residue, and/or a nucleotide analogue or equivalent, as will be further detailed herein below.
A molecule of the disclosure comprises a nucleotide-based or nucleotide or an antisense oligonucleotide sequence of between 21 and 50 nucleotides or bases, more preferred between 21 and 40 nucleotides, more preferred between 21 and 30 nucleotides, such as 21 nucleotides, 22 nucleotides, 23 nucleotides, 24 nucleotides, 25 nucleotides, 26 nucleotides, 27 nucleotides, 28 nucleotides, 29 nucleotides, 30 nucleotides, 31 nucleotides, 32 nucleotides, 33 nucleotides, 34 nucleotides, 35 nucleotides, 36 nucleotides, 37 nucleotides, 38 nucleotides, 39 nucleotides, 40 nucleotides, 41 nucleotides, 42 nucleotides, 43 nucleotides, 44 nucleotides, 45 nucleotides, 46 nucleotides, 47 nucleotides, 48 nucleotides, 49 nucleotides or 50 nucleotides. A molecule of the disclosure comprises a nucleotide-based sequence of 25 nucleotides.
In the disclosure a molecule binds to a continuous stretch of or is complementary to or is antisense to at least a continuous stretch of at least 21 nucleotides within the nucleotide sequence SEQ ID NO:2. The disclosure provides a molecule comprising or consisting of an antisense nucleotide sequence selected from the antisense nucleotide sequences as depicted in Table 1, except SEQ ID NO:68. A molecule of the disclosure that is antisense to the sequence of SEQ ID NO 2, which is present in exon 45 of the DMD gene preferably comprises or consists of the antisense nucleotide sequence of SEQ ID NO 3; SEQ ID NO 4, SEQ ID NO 5, SEQ ID NO 6, SEQ ID NO 7, SEQ ID NO 8, SEQ ID NO 9, SEQ ID NO 10, SEQ ID NO 11, SEQ ID NO 12, SEQ ID NO 13, SEQ ID NO 14, SEQ ID NO 15, SEQ ID NO 16, SEQ ID NO 17, SEQ ID NO 18, SEQ ID NO 19, SEQ ID NO 20, SEQ ID NO 21, SEQ ID NO 22, SEQ ID NO 23, SEQ ID NO 24, SEQ ID NO 25, SEQ ID NO 26, SEQ ID NO 27, SEQ ID NO 28, SEQ ID NO 29, SEQ ID NO 30, SEQ ID NO 31, SEQ ID NO 32, SEQ ID NO 33, SEQ ID NO 34, SEQ ID NO 35, SEQ ID NO 36, SEQ ID NO 37, SEQ ID NO 38, SEQ ID NO 39, SEQ ID NO 40, SEQ ID NO 41, SEQ ID NO 42, SEQ ID NO 43, SEQ ID NO 44, SEQ ID NO 45, SEQ ID NO 46, SEQ ID NO 47, SEQ ID NO 48, SEQ ID NO 49, SEQ ID NO 50, SEQ ID NO 51, SEQ ID NO 52, SEQ ID NO 53, SEQ ID NO 54, SEQ ID NO 55, SEQ ID NO 56, SEQ ID NO 57, SEQ ID NO 58, SEQ ID NO 59, SEQ ID NO 60, SEQ ID NO 61, SEQ ID NO 62, SEQ ID NO 63, SEQ ID NO 64, SEQ ID NO 65, SEQ ID NO 66 and/or SEQ ID NO:67.
The disclosure provides a molecule comprising or consisting of the antisense nucleotide sequence of SEQ ID NO 3; SEQ ID NO 4, SEQ ID NO 5, SEQ ID NO 6, SEQ ID NO 7 and/or SEQ ID NO 8.
The disclosure provides a molecule comprising or consisting of the antisense nucleotide sequence of SEQ ID NO 3. It was found that this molecule is very efficient in modulating splicing of exon 45 of the DMD pre-mRNA in a muscle cell. In a preferred embodiment, an antisense oligonucleotide is provided comprising the nucleotide sequence SEQ ID NO: 3.
A nucleotide sequence of an antisense oligonucleotide of the invention may contain a RNA residue, a DNA residue, a nucleotide analogue or equivalent as will be further detailed herein below. In addition, an antisense oligonucleotide of the invention may encompass a functional equivalent of said antisense oligonucleotide of the invention as defined herein.
It is preferred that an antisense oligonucleotide of the invention comprises a or at least one residue that is modified to increase nuclease resistance, and/or to increase the affinity of the antisense nucleotide for the target sequence. Therefore, in a preferred embodiment, an antisense nucleotide sequence comprises a or at least one nucleotide analogue or equivalent, wherein a nucleotide analogue or equivalent is defined as a residue having a modified base, and/or a modified backbone, and/or a non-natural internucleoside linkage, or a combination of these modifications.
In a preferred embodiment, a nucleotide analogue or equivalent comprises a modified backbone. Examples of such backbones are provided by morpholino backbones, carbamate backbones, siloxane backbones, sulfide, sulfoxide and sulfone backbones, formacetyl and thioformacetyl backbones, methyleneformacetyl backbones, riboacetyl backbones, alkene containing backbones, sulfamate, sulfonate and sulfonamide backbones, methyleneimino and methylenehydrazino backbones, and amide backbones. Phosphorodiamidate morpholino oligomers are modified backbone oligonucleotides that have previously been investigated as antisense agents. Morpholino oligonucleotides have an uncharged backbone in which the deoxyribose sugar of DNA is replaced by a six membered ring and the phosphodiester linkage is replaced by a phosphorodiamidate linkage. Morpholino oligonucleotides are resistant to enzymatic degradation and appear to function as antisense agents by arresting translation or interfering with pre-mRNA splicing rather than by activating RNase H. Morpholino oligonucleotides have been successfully delivered to tissue culture cells by methods that physically disrupt the cell membrane, and one study comparing several of these methods found that scrape loading was the most efficient method of delivery; however, because the morpholino backbone is uncharged, cationic lipids are not effective mediators of morpholino oligonucleotide uptake in cells. A recent report demonstrated triplex formation by a morpholino oligonucleotide and, because of the non-ionic backbone, these studies showed that the morpholino oligonucleotide was capable of triplex formation in the absence of magnesium.
It is further preferred that the linkage between a residue in a backbone does not include a phosphorus atom, such as a linkage that is formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages.
A preferred nucleotide analogue or equivalent comprises a Peptide Nucleic Acid (PNA), having a modified polyamide backbone (Nielsen, et al. (1991) Science 254, 1497-1500). PNA-based molecules are true mimics of DNA molecules in terms of base-pair recognition. The backbone of the PNA is composed of N-(2-aminoethyl)-glycine units linked by peptide bonds, wherein the nucleobases are linked to the backbone by methylene carbonyl bonds. An alternative backbone comprises a one-carbon extended pyrrolidine PNA monomer (Govindaraju and Kumar (2005) Chem. Commun, 495-497). Since the backbone of a PNA molecule contains no charged phosphate groups, PNA-RNA hybrids are usually more stable than RNA-RNA or RNA-DNA hybrids, respectively (Egholm et al (1993) Nature 365, 566-568).
A further preferred backbone comprises a morpholino nucleotide analog or equivalent, in which the ribose or deoxyribose sugar is replaced by a 6-membered morpholino ring. A most preferred nucleotide analog or equivalent comprises a phosphorodiamidate morpholino oligomer (PMO), in which the ribose or deoxyribose sugar is replaced by a 6-membered morpholino ring, and the anionic phosphodiester linkage between adjacent morpholino rings is replaced by a non-ionic phosphorodiamidate linkage.
In yet a further embodiment, a nucleotide analogue or equivalent of the invention comprises a substitution of at least one of the non-bridging oxygens in the phosphodiester linkage. This modification slightly destabilizes base-pairing but adds significant resistance to nuclease degradation. A preferred nucleotide analogue or equivalent comprises phosphorothioate, chiral phosphorothioate, phosphorodithioate, phosphotriester, aminoalkylphosphotriester, H-phosphonate, methyl and other alkyl phosphonate including 3'-alkylene phosphonate, 5'-alkylene phosphonate and chiral phosphonate, phosphinate, phosphoramidate including 3'-amino phosphoramidate and aminoalkylphosphoramidate, thionophosphoramidate, thionoalkylphosphonate, thionoalkylphosphotriester, selenophosphate or boranophosphate.
A further preferred nucleotide analogue or equivalent of the invention comprises one or more sugar moieties that are mono- or disubstituted at the 2', 3' and/or 5' position such as a -OH; -F; substituted or unsubstituted, linear or branched lower (C1-C10) alkyl, alkenyl, alkynyl, alkaryl, allyl, aryl, or aralkyl, that may be interrupted by one or more heteroatoms; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; O-, S-or N-alkynyl; O-, S-, or N-allyl; O-alkyl-O-alkyl, -methoxy, -aminopropoxy; aminoxy, methoxyethoxy; -dimethylaminooxyethoxy; and-dimethylaminoethoxyethoxy. The sugar moiety can be a pyranose or derivative thereof, or a deoxypyranose or derivative thereof, preferably a ribose or a derivative thereof, or deoxyribose or derivative thereof. Such preferred derivatized sugar moieties comprise Locked Nucleic Acid (LNA), in which the 2'-carbon atom is linked to the 3' or 4' carbon atom of the sugar ring thereby forming a bicyclic sugar moiety. A preferred LNA comprises 2'-O,4'-C-ethylene-bridged nucleic acid (Morita et al. 2001. Nucleic Acid Res Supplement No. 1: 241-242). These substitutions render the nucleotide analogue or equivalent RNase H and nuclease resistant and increase the affinity for the target RNA.
It is understood by a skilled person that it is not necessary for all positions in an antisense oligonucleotide to be modified uniformly. In addition, more than one of the aforementioned analogues or equivalents may be incorporated in a single antisense oligonucleotide or even at a single position within an antisense oligonucleotide. In certain embodiments, an antisense oligonucleotide of the invention has at least two different types of analogues or equivalents.
A preferred antisense oligonucleotide according to the invention comprises a 2'-O-alkyl phosphorothioate antisense oligonucleotide, such as 2'-O-methyl modified ribose (RNA), 2'-O-ethyl modified ribose, 2'-O-propyl modified ribose, and/or substituted derivatives of these modifications such as halogenated derivatives.
A most preferred antisense oligonucleotide according to the invention comprises a 2'-O-methyl phosphorothioate ribose.
A functional equivalent of an antisense oligonucleotide of the invention may be defined as an oligonucleotide as defined herein wherein an activity of said functional equivalent is retained to at least some extent. Preferably, an activity of said functional equivalent is inducing exon 45 skipping and providing a functional dystrophin protein. Said activity of said functional equivalent is therefore preferably assessed by detection of exon 45 skipping and quantifying the amount of a functional dystrophin protein. A functional dystrophin is herein preferably defined as being a dystrophin able to bind actin and members of the DGC protein complex. The assessment of said activity of an oligonucleotide is preferably done by RT-PCR or by immunofluorescence or Western blot analysis. Said activity is preferably retained to at least some extent when it represents at least 50%, or at least 60%, or at least 70% or at least 80% or at least 90% or at least 95% or more of corresponding activity of said oligonucleotide the functional equivalent derives from. Throughout this application, when the word oligonucleotide is used it may be replaced by a functional equivalent thereof as defined herein.
It will also be understood by a skilled person that distinct antisense oligonucleotides can be combined for efficiently skipping of exon 45 of the human DMD pre-mRNA. In a preferred embodiment, a combination of at least two antisense oligonucleotides are used in a method of the invention, such as two distinct antisense oligonucleotides, three distinct antisense oligonucleotides, four distinct antisense oligonucleotides, or five distinct antisense oligonucleotides or even more. It is also encompassed by the present disclosure to combine several oligonucleotides or molecules as depicted in table 1 except SEQ ID NO:68.
An antisense oligonucleotide can be linked to a moiety that enhances uptake of the antisense oligonucleotide in cells, preferably myogenic cells or muscle cells. Examples of such moieties are cholesterols, carbohydrates, vitamins, biotin, lipids, phospholipids, cell-penetrating peptides including but not limited to antennapedia, TAT, transportan and positively charged amino acids such as oligoarginine, poly-arginine, oligolysine or polylysine, antigen-binding domains such as provided by an antibody, a Fab fragment of an antibody, or a single chain antigen binding domain such as a cameloid single domain antigen-binding domain.
A preferred antisense oligonucleotide comprises a peptide-linked PMO.
A preferred antisense oligonucleotide comprising one or more nucleotide analogs or equivalents of the invention modulates splicing in one or more muscle cells, including heart muscle cells, upon systemic delivery. In this respect, systemic delivery of an antisense oligonucleotide comprising a specific nucleotide analog or equivalent might result in targeting a subset of muscle cells, while an antisense oligonucleotide comprising a distinct nucleotide analog or equivalent might result in targeting of a different subset of muscle cells. Therefore, in one embodiment it is preferred to use a combination of antisense oligonucleotides comprising different nucleotide analogs or equivalents for modulating skipping of exon 45 of the human DMD pre-mRNA.
In the disclosure, a cell can be provided with a molecule capable of interfering with essential sequences that result in highly efficient skipping of exon 45 of the human DMD pre-mRNA by plasmid-derived antisense oligonucleotide expression or viral expression provided by viral-based vector. Such a viral-based vector comprises an expression cassette that drives expression of an antisense oligonucleotide as defined herein. Preferred virus-based vectors include adenovirus- or adeno-associated virus-based vectors. Expression is preferably driven by a polymerase III promoter, such as a U1, a U6, or a U7 RNA promoter. A muscle or myogenic cell can be provided with a plasmid for antisense oligonucleotide expression by providing the plasmid in an aqueous solution. Alternatively, a plasmid can be provided by transfection using known transfection agentia such as, for example, LipofectAMINE™ 2000 (Invitrogen) or polyethyleneimine (PEI; ExGen500 (MBI Fermentas)), or derivatives thereof.
One preferred antisense oligonucleotide expression system is an adenovirus associated virus (AAV)-based vector. Single chain and double chain AAV-based vectors have been developed that can be used for prolonged expression of small antisense nucleotide sequences for highly efficient skipping of exon 45 of the DMD pre-mRNA.
A preferred AAV-based vector comprises an expression cassette that is driven by a polymerase III-promoter (Pol III). A preferred Pol III promoter is, for example, a U1, a U6, or a U7 RNA promoter.
The invention therefore also provides a viral-based vector, comprising a Pol III-promoter driven expression cassette for expression of one or more antisense sequences of the invention for inducing skipping of exon 45 of the human DMD pre-mRNA.
Pharmaceutical composition
If required, an antisense oligonucleotide of the invention or a vector expressing an antisense oligonucleotide of the invention can be incorporated into a pharmaceutically active mixture or composition by adding a pharmaceutically acceptable carrier.
Therefore, in a further aspect, the invention provides a composition, preferably a pharmaceutical composition comprising an antisense oligonucleotide according to the invention, and/or a viral-based vector expressing the antisense sequence(s) according to the invention and a pharmaceutically acceptable carrier.
A preferred pharmaceutical composition comprises an antisense oligonucleotide as defined herein and/or a vector as defined herein, and a pharmaceutical acceptable carrier or excipient, optionally combined with an antisense oligonucleotide and/or a vector which is able to modulate skipping of exon 7, 44, 46, 51, 53, 59, 67 of the DMD pre-mRNA.
Preferred excipients include excipients capable of forming complexes, vesicles and/or liposomes that deliver such a molecule as defined herein, preferably an oligonucleotide complexed or trapped in a vesicle or liposome through a cell membrane. Many of these excipients are known in the art. Suitable excipients comprise polyethylenimine and derivatives, or similar cationic polymers, including polypropyleneimine or polyethylenimine copolymers (PECs) and derivatives, synthetic amphiphils, lipofectinTM, DOTAP and/or viral capsid proteins that are capable of self assembly into particles that can deliver such antisense oligonucleotide as defined herein to a cell, preferably a muscle cell. Such excipients have been shown to efficiently deliver (oligonucleotide such as antisense) nucleic acids to a wide variety of cultured cells, including muscle cells. We obtained very good results using polyethylenimine (PEI, ExGen500, MBI Fermentas) as shown in the example. Their high transfection potential is combined with an excepted low to moderate toxicity in terms of overall cell survival. The ease of structural modification can be used to allow further modifications and the analysis of their further (in vivo) nucleic acid transfer characteristics and toxicity.
Lipofectin represents an example of a liposomal transfection agent. It consists of two lipid components, a cationic lipid N-[1-(2,3 dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) (cp. DOTAP which is the methylsulfate salt) and a neutral lipid dioleoylphosphatidylethanolamine (DOPE). The neutral component mediates the intracellular release. Another group of delivery systems are polymeric nanoparticles.
Polycations such like diethylaminoethylaminoethyl (DEAE)-dextran, which are well known as DNA transfection reagent can be combined with butylcyanoacrylate (PBCA) and hexylcyanoacrylate (PHCA) to formulate cationic nanoparticles that can deliver an antisense oligonucleotide across cell membranes into cells.
In addition to these common nanoparticle materials, the cationic peptide protamine offers an alternative approach to formulate an antisense oligonucleotide as colloids. This colloidal nanoparticle system can form so called proticles, which can be prepared by a simple self-assembly process to package and mediate intracellular release of an antisense oligonucleotide. The skilled person may select and adapt any of the above or other commercially available alternative excipients and delivery systems to package and deliver an antisense oligonucleotide for use in the current invention to deliver said antisense oligonucleotide for the treatment of Duchenne Muscular Dystrophy in humans.
In addition, an antisense oligonucleotide could be covalently or non-covalently linked to a targeting ligand specifically designed to facilitate the uptake in to the cell, cytoplasm and/or its nucleus. Such ligand could comprise (i) a compound (including but not limited to peptide(-like) structures) recognising cell, tissue or organ specific elements facilitating cellular uptake and/or (ii) a chemical compound able to facilitate the uptake in to cells and/or the intracellular release of an antisense oligonucleotide from vesicles, e.g. endosomes or lysosomes.
Therefore, in a preferred embodiment, an antisense oligonucleotide are formulated in a medicament which is provided with at least an excipient and/or a targeting ligand for delivery and/or a delivery device of said compound to a cell and/or enhancing its intracellular delivery. Accordingly, the invention also encompasses a pharmaceutically acceptable composition comprising a an antisense oligonucleotide and further comprising at least one excipient and/or a targeting ligand for delivery and/or a delivery device of said compound to a cell and/or enhancing its intracellular delivery. It is to be understood that an antisense oligonucleotide may not be formulated in one single composition or preparation. Depending on their identity, the skilled person will know which type of formulation is the most appropriate for each compound.
In a preferred embodiment, an in vitro concentration of an antisense oligonucleotide as defined herein, which is ranged between 0.1 nM and 1 µM is used. More preferably, the concentration used is ranged between 0.3 to 400 nM, even more preferably between 1 to 200 nM. molecule or an oligonucleotide as defined herein may be used at a dose which is ranged between 0.1 and 20 mg/kg, preferably 0.5 and 10 mg/kg. If several antisense oligonucleotides are used, these concentrations may refer to the total concentration of antisense oligonucleotides or the concentration of each antisense oligonucleotide added. The ranges of concentration of antisense oligonucleotide(s) as given above are preferred concentrations for in vitro or ex vivo uses. The skilled person will understand that depending on the antisense oligonucleotide(s) used, the target cell to be treated, the gene target and its expression levels, the medium used and the transfection and incubation conditions, the concentration of oligonucleotide(s) used may further vary and may need to be optimised any further.
More preferably, an antisense oligonucleotide and an adjunct compound to be used in the invention to prevent, treat DMD are synthetically produced and administered directly to a cell, a tissue, an organ and/or patients in formulated form in a pharmaceutically acceptable composition or preparation. The delivery of a pharmaceutical composition to the subject is preferably carried out by one or more parenteral injections, e.g. intravenous and/or subcutaneous and/or intramuscular and/or intrathecal and/or intraventricular administrations, preferably injections, at one or at multiple sites in the human body.
Use
In yet a further aspect, the invention provides the use of an antisense oligonucleotide according to the invention, and/or a viral-based vector that expresses one or more antisense sequences according to the invention and/or a pharmaceutical composition, for inducing and/or promoting splicing of the DMD pre-mRNA. The splicing is preferably modulated in a human myogenic cell or a muscle cell in vitro. More preferred is that splicing is modulated in human a myogenic cell or muscle cell in vivo.
Accordingly, the invention further relates to the use of an antisense oligonucleoitde as defined herein and/or the vector as defined herein and/or or the pharmaceutical composition as defined herein for inducing and/or promoting splicing of the DMD pre-mRNA or for the preparation of a medicament for the treatment of a DMD patient.
In this document and in its claims, the verb "to comprise" and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. In addition the verb "to consist" may be replaced by "to consist essentially of" meaning that an antisense oligonucleotide or a viral-based vector or a composition as defined herein may comprise additional component(s) than the ones specifically identified, said additional component(s) not altering the unique characteristic of the invention. In addition, reference to an element by the indefinite article "a" or "an" does not exclude the possibility that more than one of the element is present, unless the context clearly requires that there be one and only one of the elements. The indefinite article "a" or "an" thus usually means "at least one". Each embodiment as identified herein may be combined together unless otherwise indicated. All patent and literature references cited in the present specification are hereby incorporated by reference in their entirety.
The following examples are offered for illustrative purposes only, and are not intended to limit the scope of the present invention in any way.
Legends to the figure
  • Figure 1. In human control myotubes, a series of AONs (PS220 to PS225; SEQ ID NO: 3 to 8), all binding to a continuous stretch of at least 21 nucleotides within a specific sequence of exon 45 (i.e. SEQ ID NO:2), were tested at two different concentrations (200 and 500 nM). All six AONs were effective in inducing specific exon 45 skipping, as confirmed by sequence analysis (not shown). PS220 (SEQ ID NO:3) however, reproducibly induced highest levels of exon 45 skipping (see Fig. 2). (NT: non-treated cells, M: size marker).
  • Figure 2. In human control myotubes, 25-mer PS220 (SEQ ID NO: 3) was tested at increasing concentration. Levels of exon 45 skipping of up to 75% (at 400 nM) were observed reproducibly, as assessed by Agilent LabChip Analysis.
  • Figure 3. In human control myotubes, the efficiencies of a "short" 17-mer AON45-5 (SEQ ID NO:68) and its overlapping "long" 25-mer counterpart PS220 were directly compared at 200 nM and 500 nM. PS220 was markedly more efficient at both concentrations: 63% when compared to 3% obtained with 45-5. (NT: non-treated cells, M: size marker).
Examples Examples 1 and 2 Materials and methods
AON design was based on (partly) overlapping open secondary structures of the target exon RNA as predicted by the m-fold program (Zuker,M. (2003) Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res., 31, 3406-3415), and on (partly) overlapping putative SR-protein binding sites as predicted by numerous software programs such as ESEfinder (Cartegni,L. et al.(2003) ESEfinder: A web resource to identify exonic splicing enhancers. Nucleic Acids Res, 31, 3568-71; Smith,P.J. et al. (2006) An increased specificity score matrix for the prediction of SF2/ASF-specific exonic splicing enhancers. Hum.Mol.Genet., 15, 2490-2508) that predicts binding sites for the four most abundant SR proteins (SF2/ASF, SC35, SRp40 and SRp55). AONs were synthesized by Prosensa Therapeutics B.V. (Leiden, Netherlands), and contain 2'-O-methyl RNA and full-length phosphorothioate (PS) backbones.
Tissue culturing, transfection and RT-PCR analysis
Myotube cultures derived from a healthy individual ("human control") were obtained as described previously (Aartsma-Rus et al. Hum Mol Genet 2003; 12(8): 907-14). For the screening of AONs, myotube cultures were transfected with 0 to 500 nM of each AON. The transfection reagent polyethylenimine (PEI, ExGen500 MBI Fermentas) was used according to manufacturer's instructions, with 2 µl PEI per µg AON. Exon skipping efficiencies were determined by nested RT-PCR analysis using primers in the exons flanking exon 45. PCR fragments were isolated from agarose gels for sequence verification. For quantification, the PCR products were analyzed using the Agilent DNA 1000 LabChip Kit and the Agilent 2100 bioanalyzer (Agilent Technologies, USA).
Results
A series of AONs targeting sequences within SEQ ID NO:2 within exon 45 were designed and tested in normal myotube cultures, by transfection and subsequent RT-PCR and sequence analysis of isolated RNA. PS220 (SEQ ID NO: 3) reproducibly induced highest levels of exon 45 skipping, when compared to PS221-PS225 (Figure 1). High levels of exon 45 skipping of up to 75% were already obtained at 400 nM PS220 (Figure 2). In a direct comparison, PS220 (a 25-mer) was reproducibly more efficient in inducing exon 45 skipping than its shorter 17-mer counterpart AON 45-5 (SEQ ID NO: 68; previously published as h45AON5 (Aartsma-Rus et al. Am J Hum Genet 2004;74: 83-92)), at both AON concentrations of 200 nM and 500 nM and with 63% versus 3% respectively at 500 nM (Figure 3). This result is probably due to the fact that the extended length of PS220, in fact completely overlapping AON 45-5, increases the free energy of the AON-target complex such that the efficiency of inducing exon 45 skipping is also increased.
SEQ ID NO 3 (PS220) UUUGCCGCUGCCCAAUGCCAUCCUG SEQ ID NO 36 GUUGCAUUCAAUGUUCUGACAACAG
SEQ ID NO 4 (PS221) AUUCAAUGUUCUGACAACAGUUUGC SEQ ID NO 37 UUGCAUUCAAUGUUCUGACAACAGU
SEQ ID NO 5 (PS222) CCAGUUGCAUUCAAUGUUCUGACAA SEQ ID NO 38 UGCAUUCAAUGUUCUGACAACAGUU
SEQ ID NO 6 (PS223) CAGUUGCAUUCAAUGUUCUGAC SEQ ID NO 39 GCAUUCAAUGUUCUGACAACAGUUU
SEQ ID NO 7 (PS224) AGUUGCAUUCAAUGUUCUGA SEQ ID NO 40 CAUUCAAUGUUCUGACAACAGUUUG
SEQ ID NO 8 (PS225) GAUUGCUGAAUUAUUUCUUCC SEQ ID NO 41 AUUCAAUGUUCUGACAACAGUUUGC
SEQ ID NO 9 GAUUGCUGAAUUAUUUCUUCCCCAG SEQ ID NO 42 UCAAUGUUCUGACAACAGUUUGCCG
SEQ ID NO 10 AUUGCUGAAUUAUUUCUUCCCCAGU SEQ ID NO 43 CAAUGUUCUGACAACAGUUUGCCGC
SEQ ID NO 11 UUGCUGAAUUAUUUCUUCCCCAGUU SEQ ID NO 44 AAUGUUCUGACAACAGUUUGCCGCU
SEQ ID NO 12 UGCUGAAUUAUUUCUUCCCCAGUUG SEQ ID NO 45 AUGUUCUGACAACAGUUUGCCGCUG
SEQ ID NO 13 GCUGAAUUAUUUCUUCCCCAGUUGC SEQ ID NO 46 UGUUCUGACAACAGUUUGCCGCUGC
SEQ ID NO 14 CUGAAUUAUUUCUUCCCCAGUUGCA SEQ ID NO 47 GUUCUGACAACAGUUUGCCGCUGCC
SEQ ID NO 15 UGAAUUAUUUCUUCCCCAGUUGCAU SEQ ID NO 48 UUCUGACAACAGUUUGCCGCUGCCC
SEQ ID NO 16 GAAUUAUUUCUUCCCCAGUUGCAUU SEQ ID NO 49 UCUGACAACAGUUUGCCGCUGCCCA
SEQ ID NO17 AAUUAUUUCUUCCCCAGUUGCAUUC SEQ ID NO 50 CUGACAACAGUUUGCCGCUGCCCAA
SEQ ID NO 18 AUUAUUUCUUCCCCAGUUGCAUUCA SEQ ID NO 51 UGACAACAGUUUGCCGCUGCCCAAU
SEQ ID NO 19 UUAUUUCUUCCCCAGUUGCAUUCAA SEQ ID NO 52 GACAACAGUUUGCCGCUGCCCAAUG
SEQ ID NO 20 UAUUUCUUCCCCAGUUGCAUUCAAU SEQ ID NO 53 ACAACAGUUUGCCGCUGCCCAAUGC
SEQ ID NO 21 AUUUCUUCCCCAGUUGCAUUCAAUG SEQ ID NO 54 CAACAGUUUGCCGCUGCCCAAUGCC
SEQ ID NO 22 UUUCUUCCCCAGUUGCAUUCAAUGU SEQ ID NO 55 AACAGUUUGCCGCUGCCCAAUGCCA
SEQ ID NO 23 UUCUUCCCCAGUUGCAUUCAAUGUU SEQ ID NO 56 ACAGUUUGCCGCUGCCCAAUGCCAU
SEQ ID NO 24 UCUUCCCCAGUUGCAUUCAAUGUUC SEQ ID NO 57 CAGUUUGCCGCUGCCCAAUGCCAUC
SEQ ID NO 25 CUUCCCCAGUUGCAUUCAAUGUUCU SEQ ID NO 58 AGUUUGCCGCUGCCCAAUGCCAUCC
SEQ ID NO 26 UUCCCCAGUUGCAUUCAAUGUUCUG SEQ ID NO 59 GUUUGCCGCUGCCCAAUGCCAUCCU
SEQ ID NO 27 UCCCCAGUUGCAUUCAAUGUUCUGA SEQ ID NO 60 UUUGCCGCUGCCCAAUGCCAUCCUG
SEQ ID NO 28 CCCCAGUUGCAUUCAAUGUUCUGAC SEQ ID NO 61 UUGCCGCUGCCCAAUGCCAUCCUGG
SEQ ID NO 29 CCCAGUUGCAUUCAAUGUUCUGACA SEQ ID NO 62 UGCCGCUGCCCAAUGCCAUCCUGGA
SEQ ID NO 30 CCAGUUGCAUUCAAUGUUCUGACAA SEQ ID NO 63 GCCGCUGCCCAAUGCCAUCCUGGAG
SEQ ID NO 31 CAGUUGCAUUCAAUGUUCUGACAAC SEQ ID NO 64 CCGCUGCCCAAUGCCAUCCUGGAGU
SEQ ID NO 32 AGUUGCAUUCAAUGUUCUGACAACA SEQ ID NO 65 CGCUGCCCAAUGCCAUCCUGGAGUU
SEQ ID NO 33 UCC UGU AGA AUA CUG GCA UC SEQ ID NO 66 UGU UUU UGA GGA UUG CUG AA
SEQ ID NO 34 SEQ ID NO 67
SEQ ID NO 35 SEQ ID NO 68 (45-5) GCCCAAUGCCAUCCUGG
SEQ ID NO 69 AGAGCAGGUACCUCCAACAUCAAGG SEQ ID NO 91 UCAAGGAAGAUGGCAUUUCUAGUUU
SEQ ID NO 70 GAGCAGGUACCUCCAACAUCAAGGA SEQ ID NO 92 UCAAGGAAGAUGGCAUUUCU
SEQ ID NO 71 AGCAGGUACCUCCAACAUCAAGGAA SEQ ID NO 93 CAAGGAAGAUGGCAUUUCUAGUUUG
SEQ ID NO 72 GCAGGUACCUCCAACAUCAAGGAAG SEQ ID NO 94 AAGGAAGAUGGCAUUUCUAGUUUGG
SEQ ID NO 73 CAGGUACCUCCAACAUCAAGGAAGA SEQ ID NO 95 AGGAAGAUGGCAUUUCUAGUUUGGA
SEQ ID NO 74 AGGUACCUCCAACAUCAAGGAAGAU SEQ ID NO 96 GGAAGAUGGCAUUUCUAGUUUGGAG
SEQ ID NO 75 GGUACCUCCAACAUCAAGGAAGAUG SEQ ID NO 97 GAAGAUGGCAUUUCUAGUUUGGAGA
SEQ ID NO 76 GUACCUCCAACAUCAAGGAAGAUGG SEQ ID NO 98 AAGAUGGCAUUUCUAGUUUGGAGAU
SEQ ID NO 77 UACCUCCAACAUCAAGGAAGAUGGC SEQ ID NO 99 AGAUGGCAUUUCUAGUUUGGAGAUG
SEQ ID NO 78 ACCUCCAACAUCAAGGAAGAUGGCA SEQ ID NO 100 GAUGGCAUUUCUAGUUUGGAGAUGG
SEQ ID NO 79 CCUCCAACAUCAAGGAAGAUGGCAU SEQ ID NO 101 AUGGCAUUUCUAGUUUGGAGAUGGC
SEQ ID NO 80 CUCCAACAUCAAGGAAGAUGGCAUU SEQ ID NO 102 UGGCAUUUCUAGUUUGGAGAUGGCA
SEQ ID NO 81 CUCCAACAUCAAGGAAGAUGGCAUUUCUAG SEQ ID NO 103 GGCAUUUCUAGUUUGGAGAUGGCAG
SEQ ID NO 82 UCCAACAUCAAGGAAGAUGGCAUUU SEQ ID NO 104 GCAUUUCUAGUUUGGAGAUGGCAGU
SEQ ID NO 83 CCAACAUCAAGGAAGAUGGCAUUUC SEQ ID NO 105 CAUUUCUAGUUUGGAGAUGGCAGUU
SEQ ID NO 84 CAACAUCAAGGAAGAUGGCAUUUCU SEQ ID NO 106 AUUUCUAGUUUGGAGAUGGCAGUUU
SEQ ID NO 85 AACAUCAAGGAAGAUGGCAUUUCUA SEQ ID NO 107 UUUCUAGUUUGGAGAUGGCAGUUUC
SEQ ID NO 86 ACAUCAAGGAAGAUGGCAUUUCUAG SEQ ID NO 108 UUCUAGUUUGGAGAUGGCAGUUUCC
SEQ ID NO 87 ACAUCAAGGAAGAUGGCAUUUCUAGUUUGG
SEQ ID NO 88 ACAUCAAGGAAGAUGGCAUUUCUAG
SEQ ID NO 89 CAUCAAGGAAGAUGGCAUUUCUAGU
SEQ ID NO 90 AUCAAGGAAGAUGGCAUUUCUAGUU
SEQ ID NO 109 CCAUUGUGUUGAAUCCUUUAACAUU SEQ ID NO 116 CAUUCAACUGUUGCCUCCGGUUCUGAAGGUG
SEQ ID NO 110 CCAUUGUGUUGAAUCCUUUAAC SEQ ID NO 117 CUGAAGGUGUUCUUGUACUUCAUCC
SEQ ID NO 111 AUUGUGUUGAAUCCUUUAAC SEQ ID NO 118 UGUAUAGGGACCCUCCUUCCAUGACUC
SEQ ID NO 112 CCUGUCCUAAGACCUGCUCA SEQ ID NO 119 AUCCCACUGAUUCUGAAUUC
SEQ ID NO 113 CUUUUGGAUUGCAUCUACUGUAUAG SEQ ID NO 120 UUGGCUCUGGCCUGUCCUAAGA
SEQ ID NO 114 CAUUCAACUGUUGCCUCCGGUUCUG SEQ ID NO 121 AAGACCUGCUCAGCUUCUUCCUUAGCUUCCAGCCA
SEQ ID NO 115 CUGUUGCCUCCGGUUCUGAAGGUG
SEQ ID NO 122 UGCAUGUUCCAGUCGUUGUGUGG SEQ ID NO 124 AUUUACCAACCUUCAGGAUCGAGUA
SEQ ID NO 123 CACUAUUCCAGUCAAAUAGGUCUGG SEQ ID NO 125 GGCCUAAAACACAUACACAUA
SEQ ID NO 126 UCAGCUUCUGUUAGCCACUG SEQ ID NO 151 AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 127 UUCAGCUUCUGUUAGCCACU SEQ ID NO 152 CAGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 128 UUCAGCUUCUGUUAGCCACUG SEQ ID NO 153 AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 129 UCAGCUUCUGUUAGCCACUGA SEQ ID NO 154 AGCUUCUGUUAGCCACUGAU
SEQID NO 130 UUCAGCUUCUGUUAGCCACUGA SEQ ID NO 155 GCUUCUGUUAGCCACUGAUU
SEQ ID NO 131 UCAGCUUCUGUUAGCCACUGA SEQ ID NO 156 AGCUUCUGUUAGCCACUGAUU
SEQ ID NO 132 UUCAGCUUCUGUUAGCCACUGA SEQ ID NO 157 GCUUCUGUUAGCCACUGAUUA
SEQ ID NO 133 UCAGCUUCUGUUAGCCACUGAU SEQ ID NO 158 AGCUUCUGUUAGCCACUGAUUA
SEQ ID NO 134 UUCAGCUUCUGUUAGCCACUGAU SEQ ID NO 159 GCUUCUGUUAGCCACUGAUUAA
SEQ ID NO 135 UCAGCUUCUGUUAGCCACUGAUU SEQ ID NO 160 AGCUUCUGUUAGCCACUGAUUAA
SEQ ID NO 136 UUCAGCUUCUGUUAGCCACUGAUU SEQ ID NO 161 GCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 137 UCAGCUUCUGUUAGCCACUGAUUA SEQ ID NO 162 AGCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 138 UUCAGCUUCUGUUAGCCACUGAUA SEQ ID NO 163 GCUUCUGUUAGCCACUGAUUAAA
SEQ ID NO 139 UCAGCUUCUGUUAGCCACUGAUUAA SEQ ID NO 164 CCAUUUGUAUUUAGCAUGUUCCC
SEQ ID NO 140 UUCAGCUUCUGUUAGCCACUGAUUAA SEQ ID NO 165 AGAUACCAUUUGUAUUUAGC
SEQ ID NO 141 UCAGCUUCUGUUAGCCACUGAUUAAA SEQ ID NO 166 GCCAUUUCUCAACAGAUCU
SEQ ID NO 142 UUCAGCUUCUGUUAGCCACUGAUUAAA SEQ ID NO 167 GCCAUUUCUCAACAGAUCUGUCA
SEQ ID NO 143 CAGCUUCUGUUAGCCACUG SEQ ID NO 168 AUUCUCAGGAAUUUGUGUCUUUC
SEQ ID NO 144 CAGCUUCUGUUAGCCACUGAU SEQ ID NO 169 UCUCAGGAAUUUGUGUCUUUC
SEQ ID NO 145 AGCUUCUGUUAGCCACUGAUU SEQ ID NO 170 GUUCAGCUUCUGUUAGCC
SEQ ID NO 146 CAGCUUCUGUUAGCCACUGAUU SEQ ID NO 171 CUGAUUAAAUAUCUUUAUAU C
SEQ ID NO 147 AGCUUCUGUUAGCCACUGAUUA SEQ ID NO 172 GCCGCCAUUUCUCAACAG
SEQ ID NO 148 CAGCUUCUGUUAGCCACUGAUUA SEQ ID NO 173 GUAUUUAGCAUGUUCCCA
SEQ ID NO 149 AGCUUCUGUUAGCCACUGAUUAA SEQ ID NO 174 CAGGAAUUUGUGUCUUUC
SEQ ID NO 150 CAGCUUCUGUUAGCCACUGAUUAA
SEQ ID NO 175 GCUUUUCUUUUAGUUGCUGCUCUUU SEQ ID NO 203 AGGUUCAAGUGGGAUACUAGCAAUG
SEQ ID NO 176 CUUUUCUUUUAGUUGCUGCUCUUUU SEQ ID NO 204 GGUUCAAGUGGGAUACUAGCAAUGU
SEQ ID NO 177 UUUUCUUUUAGUUGCUGCUCUUUUC SEQ ID NO 205 GUUCAAGUGGGAUACUAGCAAUGUU
SEQ ID NO 178 UUUCUUUUAGUUGCUGCUCUUUUCC SEQ ID NO 206 UUCAAGUGGGAUACUAGCAAUGUUA
SEQ ID NO 179 UUCUUUUAGUUGCUGCUCUUUUCCA SEQ ID NO 207 UCAAGUGGGAUACUAGCAAUGUUAU
SEQ ID NO 180 UCUUUUAGUUGCUGCUCUUUUCCAG SEQ ID NO 208 CAAGUGGGAUACUAGCAAUGUUAUC
SEQ ID NO 181 CUUUUAGUUGCUGCUCUUUUCCAGG SEQ ID NO 209 AAGUGGGAUACUAGCAAUGUUAUCU
SEQ ID NO 182 UUUUAGUUGCUGCUCUUUUCCAGGU SEQ ID NO 210 AGUGGGAUACUAGCAAUGUUAUCUG
SEQ ID NO 183 UUUAGUUGCUGCUCUUUUCCAGGUU SEQ ID NO 211 GUGGGAUACUAGCAAUGUUAUCUGC
SEQ ID NO 184 UUAGUUGCUGCUCUUUUCCAGGUUC SEQ ID NO 212 UGGGAUACUAGCAAUGUUAUCUGCU
SEQ ID NO 185 UAGUUGCUGCUCUUUUCCAGGUUCA SEQ ID NO 213 GGGAUACUAGCAAUGUUAUCUGCUU
SEQ ID NO 186 AGUUGCUGCUCUUUUCCAGGUUCAA SEQ ID NO 214 GGAUACUAGCAAUGUUAUCUGCUUC
SEQ ID NO 187 GUUGCUGCUCUUUUCCAGGUUCAAG SEQ ID NO 215 GAUACUAGCAAUGUUAUCUGCUUCC
SEQ ID NO 188 UUGCUGCUCUUUUCCAGGUUCAAGU SEQ ID NO 216 AUACUAGCAAUGUUAUCUGCUUCCU
SEQ ID NO 189 UGCUGCUCUUUUCCAGGUUCAAGUG SEQ ID NO 217 UACUAGCAAUGUUAUCUGCUUCCUC
SEQ ID NO 190 GCUGCUCUUUUCCAGGUUCAAGUGG SEQ ID NO 218 ACUAGCAAUGUUAUCUGCUUCCUCC
SEQ ID NO 191 CUGCUCUUUUCCAGGUUCAAGUGGG SEQ ID NO 219 CUAGCAAUGUUAUCUGCUUCCUCCA
SEQ ID NO 192 UGCUCUUUUCCAGGUUCAAGUGGGA SEQ ID NO 220 UAGCAAUGUUAUCUGCUUCCUCCAA
SEQ ID NO 193 GCUCUUUUCCAGGUUCAAGUGGGAC SEQ ID NO 221 AGCAAUGUUAUCUGCUUCCUCCAAC
SEQ ID NO 194 CUCUUUUCCAGGUUCAAGUGGGAUA SEQ ID NO 222 GCAAUGUUAUCUGCUUCCUCCAACC
SEQ ID NO 195 UCUUUUCCAGGUUCAAGUGGGAUAC SEQ ID NO 223 CAAUGUUAUCUGCUUCCUCCAACCA
SEQ ID NO 196 CUUUUCCAGGUUCAAGUGGGAUACU SEQ ID NO 224 AAUGUUAUCUGCUUCCUCCAACCAU
SEQ ID NO 197 UUUUCCAGGUUCAAGUGGGAUACUA SEQ ID NO 225 AUGUUAUCUGCUUCCUCCAACCAUA
SEQ ID NO 198 UUUCCAGGUUCAAGUGGGAUACUAG SEQ ID NO 226 UGUUAUCUGCUUCCUCCAACCAUAA
SEQ ID NO 199 UUCCAGGUUCAAGUGGGAUACUAGC SEQ ID NO 227 GUUAUCUGCUUCCUCCAACCAUAAA
SEQ ID NO 200 UCCAGGUUCAAGUGGGAUACUAGCA SEQ ID NO 228 GCUGCUCUUUUCCAGGUUC
SEQ ID NO 201 CCAGGUUCAAGUGGGAUACUAGCAA SEQ ID NO 229 UCUUUUCCAGGUUCAAGUGG
SEQ ID NO 202 CAGGUUCAAGUGGGAUACUAGCAAU SEQ ID NO 230 AGGUUCAAGUGGGAUACUA
SEQ ID NO 231 CAAUUUUUCCCACUCAGUAUU SEQ ID NO 233 UCCUCAGGAGGCAGCUCUAAAU
SEQ ID NO 232 UUGAAGUUCCUGGAGUCUU
SEQ ID NO 234 GCGCUGGUCACAAAAUCCUGUUGAAC SEQ ID NO 236 GGUGAAUAACUUACAAAUUUGGAAGC
SEQ ID NO 235 CACUUGCUUGAAAAGGUCUACAAAGGA
SEQUENCE LISTING
  • <110> Academisch ziekenhuis Leiden Prosensa B.V. Prosensa Holding B.v. Prosensa Technologies B.v.
  • <120> Methods and means for efficient skipping of exon 45 in DMD pre-mRNA
  • <130> P6024691PCT
  • <150> PCT/NL2008/50673 <151> 2008-10-27
  • <160> 236
  • <170> PatentIn version 3.3
  • <210> 1 <211> 3685 <212> PRT <213> homo sapiens
  • <400> 1
  • <210> 2 <211> 75 <212> RNA <213> artificial
  • <220> <223> exon
  • <400> 2
  • <210> 3 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 3 uuugccgcug cccaaugcca uccug 25
  • <210> 4 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 4 auucaauguu cugacaacag uuugc 25
  • <210> 5 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 5 ccaguugcau ucaauguucu gacaa 25
  • <210> 6 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 6 caguugcauu caauguucug ac 22
  • <210> 7 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 7 aguugcauuc aauguucuga 20
  • <210> 8 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 8 gauugcugaa uuauuucuuc c 21
  • <210> 9 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 9 gauugcugaa uuauuucuuc cccag 25
  • <210> 10 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 10 auugcugaau uauuucuucc ccagu 25
  • <210> 11 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 11 uugcugaauu auuucuuccc caguu 25
  • <210> 12 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 12 ugcugaauua uuucuucccc aguug 25
  • <210> 13 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 13 gcugaauuau uucuucccca guugc 25
  • <210> 14 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 14 cugaauuauu ucuuccccag uugca 25
  • <210> 15 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 15 ugaauuauuu cuuccccagu ugcau 25
  • <210> 16 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 16 gaauuauuuc uuccccaguu gcauu 25
  • <210> 17 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 17 aauuauuucu uccccaguug cauuc 25
  • <210> 18 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 18 auuauuucuu ccccaguugc auuca 25
  • <210> 19 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 19 uuauuucuuc cccaguugca uucaa 25
  • <210> 20 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 20 uauuucuucc ccaguugcau ucaau 25
  • <210> 21 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 21 auuucuuccc caguugcauu caaug 25
  • <210> 22 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 22 uuucuucccc aguugcauuc aaugu 25
  • <210> 23 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 23 uucuucccca guugcauuca auguu 25
  • <210> 24 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 24 ucuuccccag uugcauucaa uguuc 25
  • <210> 25 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 25 cuuccccagu ugcauucaau guucu 25
  • <210> 26 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 26 uuccccaguu gcauucaaug uucug 25
  • <210> 27 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 27 uccccaguug cauucaaugu ucuga 25
  • <210> 28 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 28 ccccaguugc auucaauguu cugac 25
  • <210> 29 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 29 cccaguugca uucaauguuc ugaca 25
  • <210> 30 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 30 ccaguugcau ucaauguucu gacaa 25
  • <210> 31 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 31 caguugcauu caauguucug acaac 25
  • <210> 32 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 32 aguugcauuc aauguucuga caaca 25
  • <210> 33 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 33 uccuguagaa uacuggcauc 20
  • <210> 34 <211> 27 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 34 ugcagaccuc cugccaccgc agauuca 27
  • <210> 35 <211> 34 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 35 uugcagaccu ccugccaccg cagauucagg cuuc 34
  • <210> 36 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 36 guugcauuca auguucugac aacag 25
  • <210> 37 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 37 uugcauucaa uguucugaca acagu 25
  • <210> 38 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 38 ugcauucaau guucugacaa caguu 25
  • <210> 39 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 39 gcauucaaug uucugacaac aguuu 25
  • <210> 40 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 40 cauucaaugu ucugacaaca guuug 25
  • <210> 41 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 41 auucaauguu cugacaacag uuugc 25
  • <210> 42 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 42 ucaauguucu gacaacaguu ugccg 25
  • <210> 43 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 43 caauguucug acaacaguuu gccgc 25
  • <210> 44 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 44 aauguucuga caacaguuug ccgcu   25
  • <210> 45 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 45 auguucugac aacaguuugc cgcug 25
  • <210> 46 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 46 uguucugaca acaguuugcc gcugc 25
  • <210> 47 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 47 guucugacaa caguuugccg cugcc 25
  • <210> 48 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 48 uucugacaac aguuugccgc ugccc   25
  • <210> 49 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 49 ucugacaaca guuugccgcu gccca 25
  • <210> 50 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 50 cugacaacag uuugccgcug cccaa 25
  • <210> 51 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 51 ugacaacagu uugccgcugc ccaau 25
  • <210> 52 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 52 gacaacaguu ugccgcugcc caaug 25
  • <210> 53 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 53 acaacaguuu gccgcugccc aaugc   25
  • <210> 54 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 54 caacaguuug ccgcugccca augcc 25
  • <210> 55 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 55 aacaguuugc cgcugcccaa ugcca 25
  • <210> 56 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 56 acaguuugcc gcugcccaau gccau 25
  • <210> 57 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 57 caguuugccg cugcccaaug ccauc 25
  • <210> 58 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 58 aguuugccgc ugcccaaugc caucc 25
  • <210> 59 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 59 guuugccgcu gcccaaugcc auccu 25
  • <210> 60 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 60 uuugccgcug cccaaugcca uccug 25
  • <210> 61 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 61 uugccgcugc ccaaugccau ccugg 25
  • <210> 62 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 62 ugccgcugcc caaugccauc cugga 25
  • <210> 63 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 63 gccgcugccc aaugccaucc uggag 25
  • <210> 64 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 64 ccgcugccca augccauccu ggagu 25
  • <210> 65 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 65 cgcugcccaa ugccauccug gaguu 25
  • <210> 66 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligoncleotide
  • <400> 66 uguuuuugag gauugcugaa 20
  • <210> 67 <211> 40 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 67 uguucugaca acaguuugcc gcugcccaau gccauccugg 40
  • <210> 68 <211> 17 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 68 gcccaaugcc auccugg 17
  • <210> 69 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 69 agagcaggua ccuccaacau caagg 25
  • <210> 70 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 70 gagcagguac cuccaacauc aagga 25
  • <210> 71 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 71 agcagguacc uccaacauca aggaa 25
  • <210> 72 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 72 gcagguaccu ccaacaucaa ggaag   25
  • <210> 73 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 73 cagguaccuc caacaucaag gaaga 25
  • <210> 74 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 74 agguaccucc aacaucaagg aagau   25
  • <210> 75 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 75 gguaccucca acaucaagga agaug 25
  • <210> 76 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 76 guaccuccaa caucaaggaa gaugg 25
  • <210> 77 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 77 uaccuccaac aucaaggaag auggc 25
  • <210> 78 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 78 accuccaaca ucaaggaaga uggca 25
  • <210> 79 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 79 ccuccaacau caaggaagau ggcau 25
  • <210> 80 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 80 cuccaacauc aaggaagaug gcauu 25
  • <210> 81 <211> 30 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 81 cuccaacauc aaggaagaug gcauuucuag 30
  • <210> 82 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 82 uccaacauca aggaagaugg cauuu 25
  • <210> 83 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 83 ccaacaucaa ggaagauggc auuuc 25
  • <210> 84 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 84 caacaucaag gaagauggca uuucu 25
  • <210> 85 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 85 aacaucaagg aagauggcau uucua   25
  • <210> 86 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 86 acaucaagga agauggcauu ucuag 25
  • <210> 87 <211> 30 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 87 acaucaagga agauggcauu ucuaguuugg 30
  • <210> 88 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 88 acaucaagga agauggcauu ucuag 25
  • <210> 89 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 89 caucaaggaa gauggcauuu cuagu   25
  • <210> 90 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 90 aucaaggaag auggcauuuc uaguu 25
  • <210> 91 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 91 ucaaggaaga uggcauuucu aguuu 25
  • <210> 92 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 92 ucaaggaaga uggcauuucu 20
  • <210> 93 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 93 caaggaagau ggcauuucua guuug 25
  • <210> 94 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 94 aaggaagaug gcauuucuag uuugg 25
  • <210> 95 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 95 aggaagaugg cauuucuagu uugga 25
  • <210> 96 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 96 ggaagauggc auuucuaguu uggag   25
  • <210> 97 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 97 gaagauggca uuucuaguuu ggaga   25
  • <210> 98 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 98 aagauggcau uucuaguuug gagau 25
  • <210> 99 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 99 agauggcauu ucuaguuugg agaug 25
  • <210> 100 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 100 gauggcauuu cuaguuugga gaugg 25
  • <210> 101 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 101 auggcauuuc uaguuuggag auggc 25
  • <210> 102 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 102 uggcauuucu aguuuggaga uggca   25
  • <210> 103 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 103 ggcauuucua guuuggagau ggcag 25
  • <210> 104 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 104 gcauuucuag uuuggagaug gcagu 25
  • <210> 105 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 105 cauuucuagu uuggagaugg caguu 25
  • <210> 106 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 106 auuucuaguu uggagauggc aguuu 25
  • <210> 107 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 107 uuucuaguuu ggagauggca guuuc 25
  • <210> 108 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 108 uucuaguuug gagauggcag uuucc 25
  • <210> 109 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 109 ccauuguguu gaauccuuua acauu 25
  • <210> 110 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 110 ccauuguguu gaauccuuua ac 22
  • <210> 111 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 111 auuguguuga auccuuuaac 20
  • <210> 112 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 112 ccuguccuaa gaccugcuca 20
  • <210> 113 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 113 cuuuuggauu gcaucuacug uauag 25
  • <210> 114 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 114 cauucaacug uugccuccgg uucug 25
  • <210> 115 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 115 cuguugccuc cgguucugaa ggug 24
  • <210> 116 <211> 31 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 116 cauucaacug uugccuccgg uucugaaggu g   31
  • <210> 117 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 117 cugaaggugu ucuuguacuu caucc 25
  • <210> 118 <211> 27 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 118 uguauaggga cccuccuucc augacuc 27
  • <210> 119 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 119 aucccacuga uucugaauuc   20
  • <210> 120 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 120 uuggcucugg ccuguccuaa ga 22
  • <210> 121 <211> 35 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 121 aagaccugcu cagcuucuuc cuuagcuucc agcca 35
  • <210> 122 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 122 ugcauguucc agucguugug ugg 23
  • <210> 123 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 123 cacuauucca gucaaauagg ucugg 25
  • <210> 124 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 124 auuuaccaac cuucaggauc gagua 25
  • <210> 125 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 125 ggccuaaaac acauacacau a 21
  • <210> 126 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 126 ucagcuucug uuagccacug 20
  • <210> 127 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 127 uucagcuucu guuagccacu   20
  • <210> 128 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 128 uucagcuucu guuagccacu g   21
  • <210> 129 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 129 ucagcuucug uuagccacug a 21
  • <210> 130 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 130 uucagcuucu guuagccacu ga 22
  • <210> 131 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 131 ucagcuucug uuagccacug a 21
  • <210> 132 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 132 uucagcuucu guuagccacu ga 22
  • <210> 133 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 133 ucagcuucug uuagccacug au 22
  • <210> 134 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 134 uucagcuucu guuagccacu gau 23
  • <210> 135 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 135 ucagcuucug uuagccacug auu 23
  • <210> 136 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 136 uucagcuucu guuagccacu gauu   24
  • <210> 137 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 137 ucagcuucug uuagccacug auua 24
  • <210> 138 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 138 uucagcuucu guuagccacu gaua   24
  • <210> 139 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 139 ucagcuucug uuagccacug auuaa 25
  • <210> 140 <211> 26 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 140 uucagcuucu guuagccacu gauuaa   26
  • <210> 141 <211> 26 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 141 ucagcuucug uuagccacug auuaaa 26
  • <210> 142 <211> 27 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 142 uucagcuucu guuagccacu gauuaaa 27
  • <210> 143 <211> 19 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 143 cagcuucugu uagccacug   19
  • <210> 144 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 144 cagcuucugu uagccacuga u 21
  • <210> 145 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 145 agcuucuguu agccacugau u 21
  • <210> 146 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 146 cagcuucugu uagccacuga uu 22
  • <210> 147 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 147 agcuucuguu agccacugau ua 22
  • <210> 148 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonculeotide
  • <400> 148 cagcuucugu uagccacuga uua 23
  • <210> 149 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 149 agcuucuguu agccacugau uaa 23
  • <210> 150 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 150 cagcuucugu uagccacuga uuaa   24
  • <210> 151 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 151 agcuucuguu agccacugau uaaa 24
  • <210> 152 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 152 cagcuucugu uagccacuga uuaaa 25
  • <210> 153 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 153 agcuucuguu agccacugau uaaa 24
  • <210> 154 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 154 agcuucuguu agccacugau 20
  • <210> 155 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 155 gcuucuguua gccacugauu 20
  • <210> 156 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 156 agcuucuguu agccacugau u   21
  • <210> 157 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 157 gcuucuguua gccacugauu a 21
  • <210> 158 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonculeotide
  • <400> 158 agcuucuguu agccacugau ua 22
  • <210> 159 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 159 gcuucuguua gccacugauu aa 22
  • <210> 160 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 160 agcuucuguu agccacugau uaa 23
  • <210> 161 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 161 gcuucuguua gccacugauu aaa 23
  • <210> 162 <211> 24 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 162 agcuucuguu agccacugau uaaa 24
  • <210> 163 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 163 gcuucuguua gccacugauu aaa 23
  • <210> 164 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 164 ccauuuguau uuagcauguu ccc 23
  • <210> 165 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 165 agauaccauu uguauuuagc 20
  • <210> 166 <211> 19 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 166 gccauuucuc aacagaucu 19
  • <210> 167 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 167 gccauuucuc aacagaucug uca 23
  • <210> 168 <211> 23 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 168 auucucagga auuugugucu uuc 23
  • <210> 169 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 169 ucucaggaau uugugucuuu c 21
  • <210> 170 <211> 18 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 170 guucagcuuc uguuagcc 18
  • <210> 171 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 171 cugauuaaau aucuuuauau c 21
  • <210> 172 <211> 18 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 172 gccgccauuu cucaacag 18
  • <210> 173 <211> 18 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 173 guauuuagca uguuccca 18
  • <210> 174 <211> 18 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 174 caggaauuug ugucuuuc 18
  • <210> 175 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 175 gcuuuucuuu uaguugcugc ucuuu 25
  • <210> 176 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 176 cuuuucuuuu aguugcugcu cuuuu   25
  • <210> 177 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 177 uuuucuuuua guugcugcuc uuuuc   25
  • <210> 178 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 178 uuucuuuuag uugcugcucu uuucc 25
  • <210> 179 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 179 uucuuuuagu ugcugcucuu uucca 25
  • <210> 180 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 180 ucuuuuaguu gcugcucuuu uccag 25
  • <210> 181 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 181 cuuuuaguug cugcucuuuu ccagg 25
  • <210> 182 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 182 uuuuaguugc ugcucuuuuc caggu 25
  • <210> 183 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 183 uuuaguugcu gcucuuuucc agguu 25
  • <210> 184 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 184 uuaguugcug cucuuuucca gguuc 25
  • <210> 185 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 185 uaguugcugc ucuuuuccag guuca 25
  • <210> 186 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 186 aguugcugcu cuuuuccagg uucaa 25
  • <210> 187 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 187 guugcugcuc uuuuccaggu ucaag 25
  • <210> 188 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 188 uugcugcucu uuuccagguu caagu 25
  • <210> 189 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 189 ugcugcucuu uuccagguuc aagug 25
  • <210> 190 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 190 gcugcucuuu uccagguuca agugg 25
  • <210> 191 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 191 cugcucuuuu ccagguucaa guggg 25
  • <210> 192 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 192 ugcucuuuuc cagguucaag uggga 25
  • <210> 193 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 193 gcucuuuucc agguucaagu gggac 25
  • <210> 194 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 194 cucuuuucca gguucaagug ggaua 25
  • <210> 195 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 195 ucuuuuccag guucaagugg gauac 25
  • <210> 196 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 196 cuuuuccagg uucaaguggg auacu 25
  • <210> 197 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 197 uuuuccaggu ucaaguggga uacua   25
  • <210> 198 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 198 uuuccagguu caagugggau acuag 25
  • <210> 199 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 199 uuccagguuc aagugggaua cuagc 25
  • <210> 200 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 200 uccagguuca agugggauac uagca 25
  • <210> 201 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 201 ccagguucaa gugggauacu agcaa 25
  • <210> 202 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 202 cagguucaag ugggauacua gcaau 25
  • <210> 203 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 203 agguucaagu gggauacuag caaug 25
  • <210> 204 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 204 gguucaagug ggauacuagc aaugu   25
  • <210> 205 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 205 guucaagugg gauacuagca auguu 25
  • <210> 206 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 206 uucaaguggg auacuagcaa uguua 25
  • <210> 207 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 207 ucaaguggga uacuagcaau guuau   25
  • <210> 208 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 208 caagugggau acuagcaaug uuauc 25
  • <210> 209 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 209 aagugggaua cuagcaaugu uaucu 25
  • <210> 210 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 210 agugggauac uagcaauguu aucug 25
  • <210> 211 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 211 gugggauacu agcaauguua ucugc 25
  • <210> 212 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 212 ugggauacua gcaauguuau cugcu   25
  • <210> 213 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 213 gggauacuag caauguuauc ugcuu   25
  • <210> 214 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 214 ggauacuagc aauguuaucu gcuuc 25
  • <210> 215 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 215 gauacuagca auguuaucug cuucc   25
  • <210> 216 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 216 auacuagcaa uguuaucugc uuccu 25
  • <210> 217 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 217 uacuagcaau guuaucugcu uccuc   25
  • <210> 218 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 218 acuagcaaug uuaucugcuu ccucc 25
  • <210> 219 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 219 cuagcaaugu uaucugcuuc cucca 25
  • <210> 220 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 220 uagcaauguu aucugcuucc uccaa 25
  • <210> 221 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 221 agcaauguua ucugcuuccu ccaac 25
  • <210> 222 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 222 gcaauguuau cugcuuccuc caacc 25
  • <210> 223 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 223 caauguuauc ugcuuccucc aacca   25
  • <210> 224 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 224 aauguuaucu gcuuccucca accau 25
  • <210> 225 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 225 auguuaucug cuuccuccaa ccaua   25
  • <210> 226 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 226 uguuaucugc uuccuccaac cauaa 25
  • <210> 227 <211> 25 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 227 guuaucugcu uccuccaacc auaaa 25
  • <210> 228 <211> 19 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 228 gcugcucuuu uccagguuc   19
  • <210> 229 <211> 20 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 229 ucuuuuccag guucaagugg 20
  • <210> 230 <211> 19 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 230 agguucaagu gggauacua   19
  • <210> 231 <211> 21 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 231 caauuuuucc cacucaguau u 21
  • <210> 232 <211> 19 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 232 uugaaguucc uggagucuu   19
  • <210> 233 <211> 22 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 233 uccucaggag gcagcucuaa au   22
  • <210> 234 <211> 26 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 234 gcgcugguca caaaauccug uugaac 26
  • <210> 235 <211> 27 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 235 cacuugcuug aaaaggucua caaagga 27
  • <210> 236 <211> 26 <212> RNA <213> artificial
  • <220> <223> oligonucleotide
  • <400> 236 ggugaauaac uuacaaauuu ggaagc 26

Claims (19)

  1. An antisense oligonucleotide comprising the nucleotide sequence SEQ ID NO 3.
  2. An antisense oligonucleotide according to claim 1 consisting of the antisense nucleotide sequence SEQ ID NO:3.
  3. An antisense oligonucleotide according to claim 1 or 2, wherein at least one of the nucleotides is a nucleotide analogue,
  4. An antisense oligonucleotide according to any one of claims 1-3, comprising an RNA residue, and/or an DNA residue.
  5. An antisense oligonucleotide according to any one of claim 1 to 3, wherein the antisense oligonucleotide sequence comprises at least one nucleotide analogue, wherein a nucleotide analogue is defined as a residue having a modified base, and/or a modified backbone, and/or a non-natural intemucleoside linkage, or a combination of these modifications.
  6. An antisense oligonucleotide according to claim 5, wherein the nucleotide analogue has a modified base.
  7. An antisense oligonucleotide according to claim 5, wherein the nucleotide analogue has a modified backbone.
  8. An antisense oligonucleotide according to any one of claims 1-6, wherein the nucleotide analogue comprises one or more sugar moieties that are mono- or disubstituted at the 2', 3' and/or 5' position.
  9. An antisense oligonucleotide according to any of claims 1 to 8, comprising a 2'-O-alkyl substituted phosphorothioate antisense oligonucleotide.
  10. An antisense oligonucleotide according to claim 9, comprising a 2'-O methyl phosphorothioate ribose.
  11. An antisense oligonucleotide according to any one of claims 1-10, comprising a phosphorothioate antisense oligonucleotide comprising the nucleotide sequence 5' uuugccgcug cccaaugcca uccug 3' (SEQ ID NO:3) wherein the sugar moieties are each 2'-O-methyl substituted.
  12. An antisense oligonucleotide which is a phosphorothioate antisense oligonucleotide having the nucleotide sequence 5' uuugccgcug cccaaugcca uccug 3' (SEQ ID NO:3) wherein the sugar moieties are 2'-O-methyl substituted.
  13. An antisense oligonucleotide according to any one of claims 7-9, wherein the modified backbone is selected from the group consisting of a morpholino backbone, a carbamate backbone, a siloxane backbone, a sulfide backbone, a sulfoxide backbone, a sulfone backbone, a formacetyl backbone, a thioformacetyl backbone, a methyleneformacetyl backbone, a riboacetyl backbone, an alkene containing backbone, a sulfamate backbone, a sulfonate backbone, a sulfonamide backbone, a methyleneimino backbone, a methylenehydrazino backbone and an amide backbone.
  14. An antisense oligonucleotide according to any one of claims 1-10 or 13, comprising phosphorodiamidate morpholino oligomer (PMO), peptide nucleic acid, and/or locked nucleic acid.
  15. A viral-based vector, comprising an expression cassette that drives expression of the antisense oligonucleotide as defined in claim 1 or 2.
  16. A pharmaceutical composition comprising an antisense oligonucleotide as defined in any one of claims 1-14 and/or the vector of claim 15, a pharmaceutical acceptable carrier, and optionally combined with an antisense oligonucleotide which is able to induce or promote skipping of exon 7, 44, 46, 51, 53, 59, 67 (as depicted in table 2) of the dystrophin pre-mRNA of a patient.
  17. The antisense oligonucleotide as defined in any one of claims 1-14, the vector of claim 15, or the pharmaceutical composition of claim 16, for inducing or promoting exon 45 skipping, optionally in combination with skipping of one of the exons 7, 44, 46, 51, 53, 59, 67, in the dystrophin pre-mRNA for use in treating a DMD or a BMD patient.
  18. An in vitro method for inducing or promoting skipping of exon 45 of dystrophin pre-mRNA in a patient, preferably in an isolated cell of said patient, the method comprising providing said cell with an antisense oligonucleotide as defined in any one of claims 1-14, the vector of claim 15, or the pharmaceutical composition of claim 16.
  19. An in vitro method according to claim 18, wherein the patient is provided with a functional dystrophin protein and/or wherein the production of an aberrant dystrophin protein in said patient is decreased, wherein the level of said functional dystrophin is assessed by comparison to the level of said dystrophin in said patient at the onset of the method.
HK12100495.6A 2008-10-27 2009-01-13 Methods and means for efficient skipping of exon 45 in duchenne muscular dystrophy pre-mrna HK1160169B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PCT/NL2008/050673 WO2009054725A2 (en) 2007-10-26 2008-10-27 Means and methods for counteracting muscle disorders
NLPCT/NL2008/050673 2008-10-27
PCT/NL2009/050006 WO2010050801A1 (en) 2008-10-27 2009-01-13 Methods and means for efficient skipping of exon 45 in duchenne muscular dystrophy pre-mrna

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HK1160169B true HK1160169B (en) 2015-08-14

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