US20030022190A1

US20030022190A1 - Method and reagents for testing for mutations in the BRCA1 gene

Info

Publication number: US20030022190A1
Application number: US10/032,924
Authority: US
Inventors: Robert Shipman; James Leushner; James Dunn
Original assignee: Individual
Current assignee: Individual
Priority date: 1994-07-08
Filing date: 2001-12-26
Publication date: 2003-01-30
Also published as: AU2687397A; US6403303B1; CA2254892A1; WO1997043441A1

Abstract

Samples are tested for mutations in the BRCA1 gene using a hierarchical approach. First, each sample is amplified in one or more multiplex PCR amplification reactions. Each multiplex PCR reaction produces a mixture of amplified fragments. The sizes and amounts of these fragments are evaluated and compared to standard values reflecting the sizes and amounts of fragments produced when the same multiplex amplification is performed on the wild-type BRCA1 gene. Differences between the observed fragment sizes and/or amounts and those for the wild-type gene are indicative of a mutation with the BRCA1 gene of the sample. Next, one or more of the exons of the BRCA1 gene are sequenced, preferably only for those samples where no mutation was detected by analysis of the multiplex PCR fragments. The sequencing procedure can be performed by amplification and sequencing of the multiplex amplification mixture.

Description

This application is a continuation in part of U.S. patent application Ser. No. 08/271,946 filed Jul. 8, 1994 which is incorporated herein by reference.[0001]

BACKGROUND OF THE INVENTION

Genetic testing to determine the presence of or a susceptibility to a disease condition offers incredible opportunities for improved medical care, and the potential for such testing increases almost daily as ever increasing numbers of disease-associated genes and/or mutations are identified. One such disease-associated gene is the BRCA1 gene. Mutations in the BRCA1 gene have been shown to be linked to breast and ovarian cancer. Miki et al., “A Strong Candidate for the Breast Cancer and Ovarian Cancer Susceptibility Gene BRCA1 ”, Science 226: 66-71 (1994).

Since the identification of the BRCA1 gene, researchers have tested many individuals using sequencing, single-stranded conformational polymorphism, allele-specific oligonucleotide hybridization and heteroduplex analysis to identify BRCA1 mutations in families with a history of breast and ovarian cancer. Shattuck-Eidens et al., “A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene”, J. Amer. Med. Assoc. 273: 535-541 (1995). Diagnostic screening to identify persons with these mutations, and thus with an apparent genetic predisposition to breast and ovarian cancers offers the opportunity for increased monitoring of high-risk patients which should lead to earlier detection of cancer. Such early detection improves the likelihood of successful treatment and the likelihood of long-term post-detection survival. On the other hand, large scale screening could be prohibitively expensive, absent a easily-performed, low-cost test for mutations in the BRCA1 gene.

It as an object of the present invention to provide a screening methodology which can be used to provide low-cost testing for mutations in the BRCA1 gene.

It is a further object of the present invention to provide reagents, particularly primers and primer cocktails, which can be used in testing for mutations in the BRCA1 gene.

SUMMARY OF THE INVENTION

In accordance with the present invention, samples are tested for mutations in the BRCA1 gene using a hierarchical approach. First, each sample is amplified in one or more multiplex PCR amplification reactions. Each multiplex PCR reaction produces a mixture of amplified fragments. The sizes and amounts of these fragments are evaluated and compared to standard values reflecting the sizes and amounts of fragments produced when the same multiplex amplification is performed on the wild-type BRCA1 gene. Differences between the observed fragment sizes and/or amounts and those for the wild-type gene are indicative of a mutation with the BRCA1 gene of the sample.

The next step in the method of the invention is sequencing of one or more regions within the BRCA1 gene. In accordance with the hierarchical method, such sequencing will be performed on samples where no mutation was detected by analysis of the multiplex PCR fragments.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates an embodiment of the sequencing step of the method of the invention; and [0008]
FIGS. 2A and 2B illustrate two embodiments of the method of the invention in which multiplex amplification and sequencing are performed sequentially on the same initial aliquot of sample.[0009]

DETAILED DESCRIPTION OF THE INVENTION

To date, over thirty BRCA1 mutations have been identified in the breast cancer families which have been studied. A substantial number of these mutations are insertion or deletion mutations. Furthermore, 75% of the currently known mutations are found in exon 11 and an additional 5% are found in exons 2 and 20. This type of distribution makes BRCA1 well-suited for analysis using the type of hierarchical analysis described in co-pending U.S. patent application Ser. No. 08/271,946. Use of a hierarchical analysis provides highly accurate test results at a reduced cost per patient. [0010]
The first step in the hierarchical analysis is multiplex amplification and fragment length analysis of at least exons 2, 11 and 20 of the BRCA 1 gene. For multiplex amplification, a sample to be evaluated is combined with a several amplification primers. Amplification primers are selected to hybridize with the known sequence of the introns or exons of the BRCA1 gene. This sequence can be found online at the Breast Cancer Information Core, which has the following URL: http://www.nchgr.nih.gov/Intramural_research/Lab_transfer/Bic/. Information about the cDNA sequence can also be found from GenBank Accession No. U14680 or Genome Data Base Accession No. GDB: 126611. While considerable variation is theoretically possible in the sequence of these primers, the practical requirements for multiplex amplification and fragment analysis mean that primers cannot be simply selected at random. These requirements impose at least the following limitations on primers used in the method of the invention: [0011]
(1) in order to avoid the possibility of false positive results the primer pair, i.e., the combination of the 5′-primer and the 3′-primer for any given exon must be unique to the BRCA1 gene so that only the BRCA1 gene will be amplified. This means that the primer sequences will be generally somewhat longer than the minimum which can be used as an amplification primer. Preferred primers are from 18 to 23 nucleotides in length, without internal homology or primer-primer homology. [0012]
(2) It is also desirable for the primers to form more stable duplexes with the target DNA at the primers′ 3′-ends than at their 5′-ends, because this leads to less false priming. Stability can be approximated by GC content, since GC base pairs are more stable than AT pairs, or by nearest neighbor thermodynamic parameters. Breslauer et al., “Predicting DNA duplex stability from base sequence”, [0013] Proc. Nat'l Acad. Sci. USA 83: 3746-3750 (1986).
(3) To ensure complete amplification of each exon, the two primers of a pair are preferably selected to hybridize in the introns immediately flanking the exon to be amplified using the primer pair. [0014]
(4) Primer pairs are advantageously selected to have similar melting temperatures. Further, multiplex pools should contain primer pairs with approximately the same thermal profile, so that they can be effectively coamplified together. This goal can be achieved by having groups of primer pairs with approximately the same length and the same G/C content. [0015]
(5) The length of the gene region between the primer binding sites on a normal BRCA1 gene should be different for each exon to be multiplexed as a group. Differences of only one base in length are sufficient, provided a high resolution gel capable of resolving one base differences is used in analyzing the amplification products. However, greater differences in length are preferred, to avoid confusion in interpreting fragment sizes resulting from an insertion or deletion mutation. [0016]
Table 1 shows a series of amplification primers for various exons of the BRCA1 gene which meet these criteria when grouped into one of the multiplex groups as shown in the Table. It will be understood in the art that the same amplification products could be produced using primer pairs complementary to those set forth in Table 1. Because of the large size of exon 11, this exon is preferably amplified in multiple overlapping fragments using primers which bind to the exon in an interlocking manner so that all regions of the exon are amplified and analyzed, rather than using intron primers. This provides a more robust analysis, since amplification of shorter regions provides more reliable results, and also facilitates localization and identification of detected insertion or deletion mutations. Melting temperatures and optimum annealing temperatures in Table 1 are calculated assuming a salt concentration of 50 mM and 250 pM primer concentration. Conditions of actual use may be different, for example primer concentration of 200 nM to 1 μM will normally be used. Because of variations in primer and/or salt concentrations, experimental optimization using the calculated temperature as a starting point may be desirable. [0017]
While the foregoing set of primers provides the desirable ability to coamplify regions of the BRCA1 gene for fragment length analysis, it will be appreciated that other primers sets can be used as well based upon the known sequence of the BRCA1 gene by evaluating the uniqueness of the primer sequences and determining the predicted melting temperature for each primer. This can be accomplished in several ways. For example, the melting temperature, Tm can be calculated using either of the following equations: [0018]
Tm(° C.)=81.5+16.6×log [Na]+0.41×(% GC)−675/length
where [Na] is the concentration of sodium ions, and the % GC is in number percent, or [0019]
Tm(° C.)=2×(A+T)+4×(G+C)
where A, T, G, and C represent the number of adenosine, thymidine, guanosine and cytosine residues in the primer. Alternatively, OLIGO™ software can be used to calculate Tm, nearest neighbor and ΔH/ΔG values. In general, primers for coamplification should be selected to have predicted melting temperatures differing by less than 4° C. [0020]
To perform the multiplex fragment analysis, each selected set of primers is combined with an aliquot of sample in a reaction mixture containing a template-dependant DNA polymerase, such as Taq polymerase, T7 DNA Polymerase, or Thermo Sequenase®; deoxynucleoside triphosphate feedstocks (A, C, C and T); and an appropriate buffer to permit extension of the primers. The resulting reaction mixture is thermally cycled through multiple cycles of annealing (performed at or below an average of the optimum annealing temperatures listed in Table 1), primer extension (performed at about 70 to 72° C.) and denaturation (performed at a temperature of around 95° C.). In practice, each reaction condition is optimized using the predicted temperatures as a starting points, and varying the temperature within a range from about 44 to 66° C. [0021]
After sufficient cycles to produce detectable levels of amplification products, the product mixture is loaded onto a separation matrix, e.g., a polyacrylamide gel, more specifically a PAGE sequencing gel, and separated on the basis of fragment size. Labeled amplification primers, particularly of amplification primers labeled with fluorophores such a fluorescein, facilitate detection of the separated bands within the separation matrix. The size of each detected fragment is determined, and compared to the expected size of the fragments for the multiplex amplification. Deviations in size or loss of a band reflect the presence and size of an insertion or deletion mutation involving the amplified fragment forming that band. Reduction in the intensity of a band generally reflects loss of one copy of the amplified exon or region in the sample. [0022]
The amplification reaction are preferably performed in a quantitative manner. This means that, for maximum effectiveness in the method of the present invention, the amplification of the exons in the sample should be carried out only for a number of cycles during which doubling of DNA is still being achieved. [0023]
Because of the frequency of insertion and deletion mutations among the known mutations in the BRCA1 gene, the fragment analysis test may, in many instances provide all the information that is needed to provide a diagnostic result. Where no insertion or deletion mutation is detected in the fragment analysis, however, the sample is further evaluated to determine the sequence of the one or more exons (or partial exons) of the BRCA1 gene. [0024]
Sequencing can be performed in known manner, although it will preferably be performed using a chain-termination sequencing reaction as originally described by Sanger et al. More preferably, the sequencing will be performed by amplification and sequencing of an exon (or portion thereof) of the BRCA1 gene using the methodologies disclosed in U.S. patent application Ser. No. ______ filed May 1, 1996 (Attorney Docket No. VGEN.P-020), which is incorporated herein by reference. This amplification and sequencing procedure can be carried out on a fresh aliquot of the original sample, or on aliquots of one or more of the multiplex fragment analysis product mixtures. [0025]
FIG. 1 illustrates a first embodiment of the sequencing step of the present invention. As shown in FIG. 1, a sample containing a target nucleic acid polymer which is to be amplified and sequenced is combined with an amplification mixture containing two primers for an exon or portion of an exon of the BRCA1 gene, a mixture of dNTP's and thermostable polymerase in a buffer suitable for amplification. The primers may be the same primers as disclosed in Table 1, or other primers which hybridize selectively with the selected part of the BRCA1 gene. [0026]
The mixture is amplified through an initial set of cycles, for example 15-40 cycles. At this stage reagents for forming chain termination products, namely a dideoxynucleoside triphosphate (ddNTP) and optionally additional thermostable polymerase, dNTP's and a labeled sequencing primer are added and additional cycles (for example another 15-20 cycles) are performed during which both amplification and the formation of chain termination products occurs. The sequencing primer may be one of the primers disclosed in Table 1 for the exon or exon portion or some other primer which hybridizes specifically with the amplified portion of the BRCA1 gene, e.g., a nested primer. At the end of these cycles, the product mixture is evaluated to determine the lengths of the chain termination products, and hence the positions of the particular base corresponding to the ddNTP within the target nucleic acid polymer. [0027]
The thermostable polymerase used in at least the sequencing step of this amplification and sequencing process, and preferably in both steps, is one which incorporates dideoxynucleosides into an extending oligonucleotide at a rate which is no less than about 0.4 times the rate of incorporation of deoxynucleosides in the same amplification mixture. The commercially available enzyme Thermo Sequenase® is such an enzyme. [0028]
A variation of this method which may be advantageous is the use of asymmetric amplification to preferentially amplify one strand of the target nucleic acid. In this case, the primer which will produce the desired sequencing template strand is combined with the sample in an amount greater than the other primer, e.g., a 10 to 50-fold excess. More amplification cycles may be required to take full advantage of asymmetric amplification. [0029]
It may also be advantageous to biotinylate one of the primers used for amplification. When amplification is carried out with biotinylated primers, a partial separation of reagents can be accomplished prior to the introduction of the sequencing reagents by capturing the biotinylated amplification products on an avidin or streptavidin-coated support, separating the liquid medium from the support and replacing the liquid medium with the sequencing reagents. In a preferred use of this approach, the biotinylated products are captured on metal or magnetic beads, which are captured with a magnet to facilitate separation of the amplification liquid. While this step is not necessary to the method, and is not intended to accomplish complete removal of the amplification reagents, the use of this step can improve the sensitivity of the procedure by reducing the number of background oligonucleotides, particularly where a separate labeled-sequencing primer is added with the ddNTP. [0030]
FIGS. 2A and 2B illustrate two embodiments of the method of the invention. As shown in FIGS. 2A and 2B, a patient sample 1 is first subjected to multiplex PCR to produce a complex mixture of amplification products using sets of amplification primers for the BRCA1 gene as disclosed in Table 1. The products of this mixture are analyzed, to detect insertion or deletion mutations. If the results of the fragment length analysis fail to show a mutation, the sample 1 is further analyzed by sequencing a selected exon or exons. [0031]
An aliquot of the original multiplex PCR amplification mixture is used as the starting material for multiple cycles of combined amplification and sequencing. Thus, the multiplex PCR amplification mixture is combined with amplification and/or labeled sequencing primers and amplified and sequenced in a single reaction vessel. Preferably, the multiplex amplification PCR is performed using capturable primers (for example biotin-labeled primers) and separated from the multiplex amplification reagents using affinity beads (e.g. avidin-coated beads) prior to the addition of the amplification/sequencing reagents. (FIG. 2B). Additional aliquots of the multiplex reaction mixture may be processed to sequence different regions if no mutation is detected in the first sequencing step. [0032]
It should be noted that the multiplex reaction performed in the first step of this embodiment makes use of labeled primers. Fluorescence from these primers may interfere with observation of a few peaks in the sequencing ladder. This interference can be minimized by utilizing a nested sequencing primer, which produces fragments having a maximum length which is shorter than the multiplex amplification products, or by the utilization of distinguishable labels for the multiplex amplification and sequencing primers. [0033]
The fragment analysis and sequencing steps of the present invention may also be advantageously combined with additional analytical steps for evaluation mutations in the BRCA1 gene. For example, a ligation analysis of the type described in the U.S. patent application Ser. No. 08/590,503 which is incorporated herein by reference can be used before or after the fragment length analysis to detect mutations in some or all of the exons of the BRCA1 gene. Briefly, this technique makes use of a set of oligonucleotide probes which hybridize in series along the length of the exon or region being evaluated. The ligation of the probes together forms a ligation product, the size of which is evaluated. When the gene or gene fragment being analyzed corresponds to the normal sequence and thus perfectly matches the probes, all of the probes in the set are ligated together, and the ligation product has a certain resulting size. When a mutation appears in the gene, the hybridization of the probe overlapping the mutation is impaired, with the result that some or all of the ligation product is of smaller size. By evaluating the size of the ligation product, both the existence of a mutation and its approximate position can be identified. [0034]

Use of CLEAVASE (Third Wave Technologies, Inc. Madison Wis.) provides another diagnostic technique which can be used according to the invention to identify mutations in BRCA1 by determining the sizes and amounts of amplified exon fragments. CLEAVASE is an endonuclease which cuts single stranded DNA (ssDNA) molecules. Since mutant ssDNA adopts a different conformation from wild-type ssDNA, the CLEAVASE digestion products show a different array of fragments. This array of fragments can be separated and examined by electrophoresis, much like multiplex PCR fragments. The advantage of CLEAVASE is that it can detect single base substitution mutations as well as insertions and deletions. Therefore, it detects fewer false negatives than multiplex PCR, though it does not locate mutations as precisely as sequencing.

TABLE 1


	Prod	Optimum	Seq.		Sense/
	Size	Annealing	ID		Anti-	Tm	MP
Exon	(bp)	Temp (° C.)	No.	Primer	sense	(° C.)	P-1

1	234	59.1	1	GGTAGCCCCTTGGTTTCCCTC	sense	59.3	A
			2	ACGCCAGTACCCCAGACCATC	anti	57.7

2	236	46.8	3	AATGATGAAAATGAAGTTGTC	sense	43.4	B
			4	GTTCATTTGCATAGGAGATAA	anti	44.1

2	275	47.7	75	AAACCTTCCAAATCTTCAAAT	sense	46.9	C
			76	TTCTGTTCATTTGCATAGGAG	anti	47.3

2	286	46.9	75	AAACCTTCCAAATCTTCAAAT	sense	46.9	B
			77	TGTAAGGTCAATTCTGTTCAT	anti	43.8

3	116	47.3	5	GAGCCTCATTTATTTTCTTTT	sense	44.9	C
			6	TGAAGGACAAAAACAAAAGCT	anti	48.8

4	204	49.2	7	ACCTTAAATTTTTCAACAGCT	sense	45.2	E
			8	CTCTACAGAAAACACAAAATT	anti	41.0

5	202	46.6	9	GCCTTTTGAGTATTCTTTCTA	sense	43.2	B
			10	TTCTACTTTTCCTACTGTGGT	anti	42.8

6	233	48.9	11	AGGTTTTCTACTGTTGCTGCA	sense	49.5	D
			12	CAGCACTTCACTCTCATTCTT	anti	46.1

7	218	47.3	13	CATACATTTTTCTCTAACTGC	sense	41.5	C
			14	GAAGAAGAAGAAAACAAATGG	anti	45.5

8	193	50.4	15	AGGAGGAAAAGCACAGAACTG	sense	50.5	F
			16	TACTTAAAAAACCTGAGACCC	anti	45.2

9	197	46.0	17	CAAGTACATTTTTTTAACCCT	sense	43.2	B
			18	AAAGAGAGAAACATCAATCCT	anti	44.1

10	227	48.9	19	TTTGACAGTTCTGCATACATG	sense	46.0	D
			20	CAAATGGTCTTCAGAATAATC	anti	43.4

11a	314	49.6	21	CTCCAAGGTGTATGAAGTATG	sense	44.0	I
			22	CAGCCTTTTCTACATTCATTC	anti	46.2

11b	348	49.8	23	ATTACAGCATGAGAACAGCAG	sense	47.2	J
			24	GAGTCATCAGAACCTAACAGT	anti	42.2

11c	340	49.1	25	ATAGCAGCATTCAGAAAGTTA	sense	44.2	H
			26	TCAGTAACAAATGCTCCTATA	anti	42.3

11d	314	50.2	27	CTCCCCAACTTAAGCCATGTA	sense	51.2	K
			28	TCGAGTGATTCTATTGGGTTA	anti	46.8

11e	325	49.2	29	TGGTCATGAGAATAAAACAAA	sense	45.1	I
			30	TGGCATTTGGTTGTACTTTTT	anti	49.4

11f	352	51.1	31	AAGCCCACCTAATTGTACTGA	sense	48.4	L
			32	TTTGGGGTCTTCAGCATTATT	anti	50.8

11g	307	48.3	33	AAGAAGAGAAACTAGAAACAG	sense	39.5	H
			34	AATGGATACTTAAAGCCTTCT	anti	44.3

11h	332	49.2	35	AAGGGACTAATTCATCGTTGT	sense	47.2	I
			36	GTCTGTACAGGGTTGATATTA	anti	41.5

11i	255	50.4	37	TGAATGTGAACAAAAGGAAGA	sense	47.4	K
			38	ATGGGAAAAAGTGGTGGTATA	anti	48.2

11j	346	48.6	39	AACGAAACTGGACTCATTACT	sense	45.0	H
			40	TGTTTCTACCTAGTTCTGCTT	anti	43.2

11k	340	49.4	41	TGGGCTCCAGTATTAATGAAA	sense	49.4	I
			42	TCAGCAAAACTAGTATCTTCC	anti	43.5

11l	313	49.8	43	CATGCATCTCAGGTTTGTTCT	sense	49.3	J
			44	TATGCCTAGTAGACTGAGAAG	anti	40.9

11m	312	52.7	45	GCTTCCCTGCTTCCAACACTT	sense	55.0	L
			46	TGCCTCATTTGTTTGGAAGAA	anti	52.5

11n	277	52.1	47	ACAGTGCAGTGAATTGGAAGA	sense	49.7	K
			48	CTCCCCAAAAGCATAAACATT	anti	50.5

12	191	49.2	49	GCGTTTATAGTCTGCTTTTAC	sense	43.9	E
			50	TTGGAGTGGTATTCTTTTAAG	anti	43.7

13	267	50.5	51	TATTTCATTTTCTTGGTACCA	sense	44.6	F
			52	ATAAAGGGGAAGGAAAGAATT	anti	47.9

14	251	46.7	53	GAATTATCACTATCAGAACAA	sense	38.6	B
			54	CAATCAGAGTTCAATATAAAT	anti	38.3

15	393	47.4	55	CCAGCAAGTATGAAATGTCCT	sense	48.7	C
			56	CTTTATGTAGCATTCAGAGTA	anti	38.3

16	559	49.6	57	CTTAACAGAGACCAGAACTTT	sense	42.4	E
			58	TTTCCAGAATGTTGTTAAGTC	anti	43.9

17	212	48.5	59	CTAGTATTCTGAGCTGTGTGC	sense	44.3	D
			60	CCTCGCCTCATGTCGTTTTAT	anti	53.3

18	258	48.9	61	CTCTTTAGCTTCTTAGGACAG	sense	42.8	D
			62	CTCAAGACTCAAGCATCAGCA	anti	50.6

19	215	50.5	63	TGTGAATCGCTGACCTCTCTA	sense	50.0	F
			64	AAGTGGTGCATTGATGGAAGG	anti	53.9

20	169	52.0	65	TCTCTTATCCTGATGGCTGTG	sense	49.0	G
			66	ATACAGAGTGGTGGGGTGAGA	anti	50.8

21	167	56.4	67	CAGTGGTGCGATCTCAGCTCA	sense	56.2	A
			68	AAGGCTGGTGCTGGAACTCTG	anti	55.8

22	273	51.0	69	TAGAGGGCCTGGGTTAAGTAT	sense	49.3	G
			70	GAGAAGACTTCTGACGCTACC	anti	46.6

23	152	51.1	71	CCTACTTTGACACTTTGAATG	sense	44.3	G
			72	AATGTGCCAAGAACTGTGCTA	anti	50.1

24	252	50.9	73	TAATCTCTGCTTGTGTTCTCT	sense	43.4	F
			74	GTAGCCAGGACAGTAGAAGGA	anti	47.9

EXAMPLE 1

Individual exons of the BRCA1 gene are amplified as follows. [0036]
5 ul of patient sample genomic DNA (20 ng/ul) is combined with 2 ul 10X PCR Buffer, 0.6 ul 50 mM Mg2+, 0.4 ul 10 mM dNTP mix (containing each of the 4 dNTPs), 1 ul DMSO (100%), and 8 ul ddH2O. 2 ul of a 50 ng/ul mixture of an amplification primer pair (i.e. 100 ng each primer), one of which is labeled with a detectable label, are added to the mix. The amplification primer pair is one of the pairs of exons designated in table 1 as being specific for a particular exon. A suitable label is fluorescein, which can be detected on an A.L.F. automated DNA sequencer (Pharmacia, Inc., Piscataway, N.J.). [0037]
The mixture is prepared on ice. Addition of 1 ul Taq Polymerase (1 U/ul) (Roche Molecular Systems, Inc.), bringing the total volume to 20 ul, is followed by thermal cycling as follows: [0038]
Initial denaturation 94C 10 min [0039]

Cycle (20 - 35 times):

anneal *47C 40 sec

extend 72C 60 sec

aenature 94C 30 sec

Final extension 72C 10 min then hold at room

temperature.
An equal volume of Stop Solution comprising Formamide and a visible dye is added after the reaction is complete. 6 ul of this mixture is loaded into a single lane of an A.L.F. Sequencing Gel, and the reaction products are detected. [0040]

EXAMPLE 2

Multiplex amplification of selected exons or parts of exons of BRCA1 is achieved as follows: [0041]
5 ul of patient sample genomic DNA (20 ng/ul) is combined with 2 ul 10X PCR Buffer, 0.6 ul 50 mM Mg2+, 0.4 ul 10 mM dNTP mix (containing equimolar amounts of each of the 4 dNTPs), 1 ul DMSO (100%), and 8 ul ddH2O. 2 ul of a mixture containing 50 ng/ul of a multiplex set of primers as indicated in Table 1, (i.e. 100 ng each primer), one of each pair being labeled with a detectable label, are added to the mix. A suitable label is fluorescein, which can be detected on an A.L.F. automated DNA sequencer (Pharmacia, Inc., Piscataway, N.J.). [0042]
The mixture is prepared on ice. Addition of 1 ul Taq Polymerase (1 U/ul) (Roche Molecular Systems, Inc.), bringing the total volume to 20 ul, is followed by thermal cycling as follows: [0043]
Initial denaturation 94C 10 min [0044]

Cycle (20-35 times)

anneal *47C 40 sec

extend 72C 60 sec

denature 94C 30 sec

Final extension 72C 10 min then hold at room

temperature.
An equal volume of Stop Solution comprising formamide and a visible dye is added after the reaction is complete. 6 ul of this mixture is loaded into a single lane of an A.L.F. Sequencing Gel, and the reaction products are detected. [0045]

EXAMPLE 3

Sequencing of an individual exon of BRCA1 is achieved as follows. [0046]
Amplified, biotinylated PCR product is prepared as a template for sequencing by generating the following mixture: 300 ng genomic DNA (patient sample); 1X Taq polymerase Buffer (final: 10 mM Tris-HCl, pH 8.3, 50 mM KC1, 1.5 mM MgCl2, 0.001% gelatin); and 0.2 mM each dNTP. To this mixture is added 8 pMol of each primer selected from table 1 to amplify a specific exon of BRCA1, one of which primers is biotinylated. The reaction mixture is kept on ice until the addition of 2.5U Taq DNA polymerase. The final volume is 25 ul. [0047]
This reaction mixture is thermal cycled in a Perkin Elmer 9600 as follows: [0048]

94° C. 2 min x1 cycle

94° C. 30 sec

*50° C. 30 sec x35 cycles

65° C. 2 min

65° C. 7 min x1 cycle
At the end of the reaction, a 5 ul aliquot may be taken and observed on a 1% agarose gel containing ethidium bromide to assess integrity of the amplification reaction. [0049]
If the PCR product appears satisfactory, the reaction buffer is exchanged using streptavidin/magnetic beads as follows: [0050]
1. take 8 ul of streptavidin beads (Dynal), wash with 50 ul 2×BW buffer [0051]
2. resuspend beads in 10 ul of 2×BW buffer [0052]
3. remove 10 ul of PCR product from above and mix with washed beads. [0053]
4. sit at RT for up to 1 hour with periodic mixing by gently tapping side of tube [0054]
5. place on magnetic rack, allow PCR bound-beads to separate and remove supernatant. Wash with 50 ul of 1×BW buffer, separate on magnetic rack and remove supernatant. Repeat with 50 ul of TE. [0055]
6. resuspend bound beads in 10 ul of dH20. [0056]
7. use 3 ul for cycle sequencing [0057]
*2×BW buffer: Binding/Washing buffer; 10 mM Tris pH 7.5, 1 mM EDTA, 2M NaCl [0058]
The amplification products are then ready for sequencing as follows. A reaction mixture is prepared consisting of 2 ul T7 Thermo Sequenase™ buffer (Amersham Life Sciences, Cleveland) (final: 26 mM Tris-HCl, pH 9.5, 6.5 mM MgCl2); 3 ul of PCR product from above; 3 ul (final: ˜30 ng/5 pM) Fluoresceinated primer; 3 ul dH2O; and 2 ul diluted Thermo Sequenase™ enzyme (Amersham Life Sciences, Cleveland) (final 6.4U). The total volume of 13 ul is kept on ice. [0059]
The fluoresceinated primer used has the same sequence as the non-biotinylated primer used in the amplification reaction, above, but it is fluoresceinated so that it may be detected on an A.L.F. Automated DNA Sequencing Apparatus (Pharmacia, Inc.; Piscataway, N.J.) [0060]
The reagents are mixed well, and a 3 ul aliquot is added to each of the 4 termination reaction tubes containing 3 ul of Termination Mix. The final volume of 6 ul is covered with 10 ul mineral oil before thermal cycling. [0061]
The d/ddA Termination mix contains 750 uM dNTPs, 2.5 uM ddATP. [0062]
The d/ddC Termination mix contains 750 uM dNTPs, 2.5 uM ddCTP. [0063]
The d/ddG Termination mix contains 750 uM dNTPs, 2.5 uM ddGTP. [0064]
The d/ddT Termination mix contains 750 uM dNTPs, 2.5 uM ddTTP. [0065]
The sequencing reactions are then thermal cycled in a Perkin Elmer 9600 as follows: [0066]

94° C. 2 min x1 cycle

94° C. 30 sec

*50° C. 10 sec cycle 25 times

70° C. 30 sec

70° C. 2 min x1 cycle
After the cycle sequencing reaction is complete, 6 ul of STOP buffer comprising dextran blue in formamide is added to the reaction mixture. 6 ul or half of the reaction products are loaded onto an A.L.F. Sequencer. [0067]

EXAMPLE 4

Single-Tube Sequencing of a BRCA1 exon may be achieved as follows. [0068]
The primer pair is selected from table 1 and is specific for the designated exon of BRCA1. Asymmetric amplification of the sequencing template strand is obtained using an excess ratio (10-50 fold) of template strand primer compared to the non-template strand primer. The following reactants were combined in an Eppendorf tube at 4 degrees C. in the following amounts: [0069]
300 ng patient sample genomic DNA [0070]
Primer 1: 1 pmole [0071]
Primer 2: 20 pmole [0072]
1×Thermo Sequenase™ buffer (Amersham Life Sciences, Cleveland) (final: 26 mM Tris-HCl, pH 9.5, 6.5 mM MgCl2) 5% DMSO [0073]
0.2 mM dNTPs (i.e. 0.05 of each dATP, dCTP, dGTP, dTTP) [0074]
0.25 units Thermo Sequenase™ enzyme (Amersham Life Sciences, Cleveland) [0075]
Final reaction volume: 4 microliters. This small volume allowed for the reaction to proceed close to completion, and particularly to consume available dNTPs during the amplification step. The reaction was overlaid with 10 microliters of Chill Out Liquid Wax. [0076]
The reaction tube was place in a Perkin-Elmer 9600 Thermo-Cycling apparatus and thermal cycled as follows: [0077]

94° C. 2 min x1 cycle

94° C. 30 sec

*60° C. 30 sec x39 cycles

72° C. 2 min

65° C. 7 min x1 cycle
After thermal cycling, the reaction vessel was cooled to 4 C for 10 min, whereupon the Chill Out Wax solidified and prevented any PCR carry over of product which could lead to contamination. [0078]
6 microliters of the following sequencing mix was then added: [0079]
1.2 microliters: Sequencing Primer (20 pmole) [0080]
1.0 microliters concentrated Thermo Sequenase™ buffer (Amersham Life Sciences, Cleveland) (final: 26 mM Tris-HCl, pH 9.5, 6.5 mM MgCl2) [0081]
1.0 microliters thermal stable polymerase (Thermo Sequenase) (3 units) [0082]
1.0 microliters 20% (v/v) DMSO [0083]
3.0 microliters 1:100 ratio of ddNTP and 4 dNTPs (final concentrations of 2.5 microM and 250 microM respectively). [0084]
The Sequencing primer selected was a fluoresceinated version of the subservient primer (i.e. the one originally added in lesser amount). The fluorescent label allows for detection of reaction products in an automated DNA sequencer, such as the Pharmacia A.L.F. [0085]
The ddNTP selected corresponds to the desired termination reaction, and is either ddATP, ddCTP, ddGTP or ddTTP. [0086]
The reaction was thermal cycled at the following temperatures in a Perkin-Elmer 9600 thermal cycling apparatus for 15 cycles [0087]
95° C. 15 sec [0088]
50° C. 5 sec [0089]
70° C. 15 sec [0090]
After the thermal cycles, the reaction was cooled to 4 C. It was mixed with 6 microliters stop solution (formamide and glycerol), and 1-3 (up to 10) microliters were loaded per lane of an A.L.F. automated sequencer. [0091]

EXAMPLE 5

Multiplex amplification of fragments of exon 11 listed in Table 1 as fragments 11b, 11d, 11i and 11l, of BRCA1 was achieved as follows: [0092]
5 ul of patient sample genomic DNA (20 ng/ul) was combined with 2 ul 10X PCR Buffer, 0.6 ul 50 mM Mg2+, 0.4 ul 10 mM dNTP mix (containing each of the 4 dNTPs), 1 ul DMSO (100%), and 6 ul ddH2O. 1 ul of a mixture containing 50 ng/ul of each primer pair (indicated in Table 1), (i.e. 50 ng each primer), one of each pair being labeled on its 5′ end with a fluorescein label, was added to the mix, totaling 4 ul (1 ul for each primer pair). [0093]
The mixture was prepared on ice. Addition of 1 ul Taq Polymerase (1 U/ul) (Roche Molecular Systems, Inc.), brought the total volume to 20 ul, and was followed by thermal cycling as follows: [0094]
Initial denaturation 94C 10 min [0095]

Cycle (20-35 times)

anneal 50 C 40 sec

extend 72 C 60 sec

denature 94 C 30 sec
Final extension 72C 10 min then held at room temperature. [0096]
An equal volume of Stop Solution comprising formamide and a visible dye was added after the reaction was completed. 6 ul of this mixture was loaded into a single lane of an A.L.F. Sequencing Gel, and the reaction products were detected on an A.L.F. automated DNA sequencer (Pharmacia, Inc., Piscataway, N.J.). [0097]

EXAMPLE 6

The procedure of Example 2 is repeated, using a combination of primers identified by Sequence ID Nos. 3, 4, 65 and 66 to perform a multiplex amplification of exons 2 and 20. [0098]
1 77 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 1 GGTAGCCCCT TGGTTTCCGT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 2 ACGCCAGTAC CCCAGAGCAT C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 3 AATGATGAAA ATGAAGTTGT C 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 4 GTTCATTTGC ATAGGAGATA A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 5 GAGCCTCATT TATTTTCTTT T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 6 TGAAGGACAA AAACAAAAGC T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 7 ACCTTAAATT TTTCAACAGC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 8 CTCTACAGAA AACACAAAAT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 9 GCCTTTTGAG TATTCTTTCT A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 10 TTCTACTTTT CCTACTGTGG T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 11 AGGTTTTCTA CTGTTGCTGC A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 12 CAGCACTTCA CTCTCATTCT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 13 CATACATTTT TCTCTAACTG C 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 14 GAAGAAGAAG AAAACAAATG G 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 15 AGGAGGAAAA GCACAGAACT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 16 TACTTAAAAA ACCTGAGACC C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 17 CAAGTACATT TTTTTAACCC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 18 AAAGAGAGAA ACATCAATCC T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 19 TTTGACAGTT CTGCATACAT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 20 CAAATGGTCT TCAGAATAAT C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 21 CTCCAAGGTG TATGAAGTAT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 22 CAGCCTTTTC TACATTCATT C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 23 ATTACAGCAT GAGAACAGCA G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 24 GAGTCATCAG AACCTAACAG T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 25 ATAGCAGCAT TCAGAAAGTT A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 26 TCAGTAACAA ATGCTCCTAT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 27 CTCCCCAACT TAAGCCATGT A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 28 TCGAGTGATT CTATTGGGTT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 29 TGGTCATGAG AATAAAACAA A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 30 TGGCATTTGG TTGTACTTTT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 31 AAGCCCACCT AATTGTACTG A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 32 TTTGGGGTCT TCAGCATTAT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 33 AAGAAGAGAA ACTAGAAACA G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 34 AATGGATACT TAAAGCCTTC T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 35 AAGGGACTAA TTCATGGTTG T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 36 GTCTGTACAG GCTTGATATT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 37 TGAATGTGAA CAAAAGGAAG A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 38 ATGGGAAAAA GTGGTGGTAT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 39 AACGAAACTG GACTCATTAC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 40 TGTTTCTACC TAGTTCTGCT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 41 TGGGCTCCAG TATTAATGAA A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 42 TCAGCAAAAC TAGTATCTTC C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 43 CATGCATCTC AGGTTTGTTC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 44 TATGCCTAGT AGACTGAGAA G 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 45 GCTTCCCTGC TTCCAACACT T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 46 TGCCTCATTT GTTTGGAAGA A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 47 ACAGTGCAGT GAATTGGAAG A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 48 CTCCCCAAAA GCATAAACAT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 49 GCGTTTATAG TCTGCTTTTA C 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 50 TTGGAGTGGT ATTCTTTTAA G 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 51 TATTTCATTT TCTTGGTACC A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 52 ATAAAGGGGA AGGAAAGAAT T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 53 GAATTATCAC TATCAGAACA A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 54 CAATCAGAGT TCAATATAAA T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 55 CCAGCAAGTA TGAAATGTCC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 56 CTTTATGTAG GATTCAGAGT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 57 CTTAACAGAG ACCAGAACTT T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 58 TTTCCAGAAT GTTGTTAAGT C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 59 CTAGTATTCT GAGCTGTGTG C 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 60 CCTCGCCTCA TGTGGTTTTA T 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 61 CTCTTTAGCT TCTTAGGACA G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 62 CTCAAGACTC AAGCATCAGC A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 63 TGTGAATCGC TGACCTCTCT A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 64 AAGTGGTGCA TTGATGGAAG G 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 65 TCTCTTATCC TGATGGGTGT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 66 ATACAGAGTG GTGGGGTGAG A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 67 CAGTGGTGCG ATCTCAGCTC A 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 68 AAGGCTGGTG CTGGAACTCT G 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 69 TAGAGGGCCT GGGTTAAGTA T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 70 GAGAAGACTT CTGACGCTAC C 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 71 CCTACTTTGA CACTTTGAAT G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 72 AATGTGCCAA GAACTGTGCT A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 73 TAATCTCTGC TTGTGTTCTC T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 74 GTAGCCAGGA CAGTAGAAGG A 21 21 nucleic acid double linear other nucleic acid no no internal human amplification primer for BRCA1 gene 75 AAACCTTCCA AATCTTCAAA T 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 76 TTCTGTTCAT TTGCATAGGA G 21 21 nucleic acid double linear other nucleic acid no yes internal human amplification primer for BRCA1 gene 77 TGTAAGGTCA ATTCTGTTCA T 21

Claims

We claim:

1. A method for testing a sample for mutations in the BRCA1 gene comprising the steps of

(a) amplifying one or more exons or partial exons of BRCA1 to produce amplified fragments;

(b) determining the sizes and amounts of the amplified fragments and comparing the determined sizes or amounts to standard values for amplification of the same exons or partial exons of wild-type BRCA1 gene, wherein a difference in fragment size or amount is indicative of the presence of a mutation in the BRCA1 gene; and

(c) if no mutation is detected in the BRCA1 gene as a result of the determination of the sizes and amounts of the amplification fragments, determining the sequence of one or more exons of the BRCA1 gene.

2. The method according to claim 1, wherein at least exons 2, 11 and 20, or portions thereof, are amplified to produce amplification fragments.

3. The method according to claim 1, wherein two or more exons or partial exons are amplified in a multiplex amplification reaction to produce multiplex amplification products.

4. The method according to claim 3, wherein exons 1 and 21 of the BRCA1 gene are amplified in one multiplex amplification reaction.

5. The method according to claim 4, wherein exons 1 and 21 are amplified using the primers identified by Sequence ID Nos. 1, 2, 67 and 68, or primers complementary thereto.

6. The method according to claim 3, wherein exons 2, 5, 9 and 14 of the BRCA1 gene are amplified in one multiplex amplification reaction.

7. The method according to claim 6, wherein exons 2, 5, 9 and 14 are amplified using the primers identified by Sequence ID Nos. 3, 4, 9, 10, 17, 18, 53 and 54, or primers complementary thereto.

8. The method according to claim 3, wherein exons 3, 7 and 15 of the BRCA1 gene are amplified in one multiplex amplification reaction.

9. The method according to claim 8, wherein exons 3, 7, and 15 are amplified using the primers identified by Sequence ID Nos. 5, 6, 13, 14, 55, and 56, or primers complementary thereto.

10. The method according to claim 3, wherein exons 6, 10, 17 and 18 of the BRCA1 gene are amplified in one multiplex amplification reaction.

11. The method according to claim 10, wherein exons 6, 10, 17 and 18 are amplified using the primers identified by Sequence ID Nos. 11, 12, 19, 20, 59, 60, 61 and 62, or primers complementary thereto.

12. The method according to claim 3, wherein exons 4, 12 and 16 of the BRCA1 gene are amplified in one multiplex amplification reaction.

13. The method according to claim 12, wherein exons 4, 12, and 16 are amplified using the primers identified by Sequence ID Nos. 7, 8, 49, 50, 57 and 58, or primers complementary thereto.

14. The method according to claim 3, wherein exons 8, 13, 19 and 24 of the BRCA1 gene are amplified in one multiplex amplification reaction.

15. The method according to claim 14, wherein exons 8, 13, 19 and 24 are amplified using the primers identified by Sequence ID Nos. 15, 16, 51, 52, 63, 64, 73 and 74, or primers complementary thereto.

16. The method according to claim 3, wherein exons 20, 22, and 23 of the BRCA1 gene are amplified in one multiplex amplification reaction.

17. The method according to claim 6, wherein exons 20, 22, and 23 are amplified using the primers identified by Sequence ID Nos. 65, 66, 69, 70, 71 and 72, or primers complementary thereto.

18. The method according to claim 3, wherein exons 2 and 20 are amplified in one multiplex amplification reaction.

19. The method according to claim 3, wherein the sequence is determined by amplifying a selected one of the multiplex amplification products in an aliquot of the multiplex reaction mixture and then sequencing the amplified multiplex amplification products.

20. The method according to claim 19, wherein the amplification of the multiplex reaction mixture and the sequencing of the amplified multiplex reaction product are performed in a single vessel.

21. The method according to claim 19, wherein the multiplex reaction mixture is amplified by combining the multiplex reaction mixture with an amplification mixture containing two primers for the selected one of the multiplex reaction products, a mixture of dNTP's and a thermostable polymerase in a buffer suitable for amplification, and exposing the resulting combination to a first series of thermal cycles including at least an extension phase and a denaturation phase to produce an amplified mixture containing the amplified multiplex reaction product; adding a sequencing mixture comprising a chain terminating nucleoside triphosphate to the amplified mixture and exposing the resulting combination to a second series of thermal cycles including at least an extension phase and a denaturation phase to produce sequencing fragments; and evaluating the size of the sequencing fragments.

22. The method according to claim 21, wherein the thermostable polymerase is Thermo Sequenase®.

23. The method according to claim 21, wherein the sequencing mixture further comprises a fluorescently labeled sequencing primer.

24. The method according to claim 23, wherein the sequencing mixture further comprises a thermostable polymerase for sequencing which incorporates dideoxynucleosides into an extending oligonucleotide at a rate which is no less than about 0.4 times the rate of incorporation of deoxynucleosides in an amplification mixture.

25. The method according to claim 24, wherein the thermostable polymerase for sequencing is Thermo Sequenase®

26. A kit for testing a sample for mutations in the BRCA1 gene comprising a mixture of at least four oligonucleotide primers, said primers being selected to amplify at least two different exons or portions of exons of the BRCA1 gene in a multiplex amplification reaction.

27. The kit according to claim 26, wherein the primers are selected for amplification of exons 1 and 21 of the BRCA1 gene in one multiplex amplification reaction.

28. The kit according to claim 27, wherein the primers are for amplification of exons 1 and 21 are the primers identified by Sequence ID Nos. 1, 2, 69 and 70, or primers complementary thereto.

29. The kit according to claim 26, wherein the primers are selected for amplification of exons 2, 5, 9 and 14 of the BRCA1 gene in one multiplex amplification reaction.

30. The kit according to claim 29, wherein the primers for amplification of exons 2, 5, 9 and 14 are the primers identified by Sequence ID Nos. 3, 4, 9, 10, 17, 18, 55 and 56, or primers complementary thereto.

31. The kit according to claim 26, wherein the primers are selected for amplification of exons 3, 7 and 15 of the BRCA1 gene in one multiplex amplification reaction.

32. The kit according to claim 31, wherein the primers for amplification of exons 3, 7 and 15 are the primers identified by Sequence ID Nos. 5, 6, 13, 14, 57, and 58, or primers complementary thereto.

33. The kit according to claim 26, wherein the primers are selected for amplification of exons 6, 10, 17 and 18 of the BRCA1 gene in one multiplex amplification reaction.

34. The kit according to claim 33, wherein primers for amplification of exons 6, 10, 17 and 18 are the primers identified by Sequence ID Nos. 11, 12, 19, 20, 61, 62, 63 and 64, or primers complementary thereto.

35. The kit according to claim 26, wherein the primers are selected for amplification of exons 4, 12 and 16 of the BRCA1 gene in one multiplex amplification reaction.

36. The kit according to claim 35, wherein the primers for amplification of exons 4, 12, and 16 are the primers identified by Sequence ID Nos. 7, 8, 51, 52, 59 and 60, or primers complementary thereto.

37. The kit according to claim 26, wherein the primers are selected for amplification of exons 8, 13, 19 and 24 of the BRCA1 gene in one multiplex amplification reaction.

38. The kit according to claim 37, wherein the primers for amplification of exons 8, 13, 19 and 24 are the primers identified by Sequence ID Nos. 15, 16, 53, 54, 65, 66, 75 and 76, or primers complementary thereto.

39. The kit according to claim 26, wherein the primers are selected for amplification of exons 20, 22, and 23 of the BRCA1 gene in one multiplex amplification reaction.

40. The kit according to claim 39, wherein the primers for amplification of exons 20, 22, and 23 are the primers identified by Sequence ID Nos. 67, 68, 71, 72, 73 and 74, or primers complementary thereto.

41. The kit according to claim 26, wherein the primers are selected for amplification of exons 2 and 20 in one multiplex amplification reaction.

42. The kit according to claim 41, wherein the primers for amplification of exons 2 and 20 are the primers identified by Sequence ID Nos.: 3, 4, 65 and 66.

43. An oligonucleotide primer having the sequence as set forth in any one of Sequence ID Nos. 1 through 77.

44. A method for testing a sample for mutations in the BRCA1 gene comprising the steps of

(b) determining the sizes and amounts of the amplified fragments and comparing the determined sizes or amounts to standard values for amplification of the same exons or partial exons of wild-type BRCA1 gene, wherein a difference in fragment size or amount is indicative of the presence of a mutation in the BRCA1 gene.

45. The method according to claim 44, wherein the amplification step is performed using two or more primers having the sequences as set forth Sequence ID Nos. 1 through 76.

46. The method according to claim 44, wherein two or more exons or partial exons are amplified in a multiplex amplification reaction to produce multiplex amplification products.

47. The method according to claim 46, further comprising the step of determining the sequence a selected one of the multiplex amplification products, wherein the sequence is determined by amplifying the selected one of the multiplex amplification products in an aliquot of the multiplex reaction mixture and then sequencing the amplified multiplex amplification products.

48. The method according to claim 47, wherein the multiplex reaction mixture is amplified by combining the multiplex reaction mixture with an amplification mixture containing two primers for the selected one of the multiplex reaction products, a mixture of dNTP's and a thermostable polymerase in a buffer suitable for amplification, and exposing the resulting combination to a first series of thermal cycles including at least an extension phase and a denaturation phase to produce an amplified mixture containing the amplified multiplex reaction product; adding a sequencing mixture comprising a chain terminating nucleoside triphosphate to the amplified mixture and exposing the resulting combination to a second series of thermal cycles including at least an extension phase and a denaturation phase to produce sequencing fragments; and evaluating the size of the sequencing fragments.

49. The method according to claim 49, wherein the thermostable polymerase is Thermo Sequenase®.

50. The method according to claim 49, wherein the sequencing mixture further comprises a fluorescently labeled sequencing primer.

51. The method according to claim 51, wherein the sequencing mixture further comprises a thermostable polymerase for sequencing which incorporates dideoxynucleosides into an extending oligonucleotide at a rate which is no less than about 0.4 times the rate of incorporation of deoxynucleosides in an amplification mixture.

52. The method according to claim 52, wherein the thermostable polymerase for sequencing is Thermo Sequenase®