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KR920703118A - 유전자 발현에 영향을 주는 다수의 표적반응요소를 가진 벡터 - Google Patents

유전자 발현에 영향을 주는 다수의 표적반응요소를 가진 벡터

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Publication number
KR920703118A
KR920703118A KR1019920701696A KR920701696A KR920703118A KR 920703118 A KR920703118 A KR 920703118A KR 1019920701696 A KR1019920701696 A KR 1019920701696A KR 920701696 A KR920701696 A KR 920701696A KR 920703118 A KR920703118 A KR 920703118A
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dna construct
virus
target response
construct
cells
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KR1019920701696A
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KR0148782B1 (ko
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쥴리아나 리스지바쯔
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원본미기재
더 유나이티드 스테이트 오브 어메리카 에즈 리프리젠티드 바이 더 세크리터리 유.에스 디파트먼트 오브 컴머스
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Publication of KR920703118A publication Critical patent/KR920703118A/ko
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Publication of KR0148782B1 publication Critical patent/KR0148782B1/ko

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Abstract

내용 없음

Description

유전자 발현에 영향을 주는 다수의 표적반응요소를 가진 벡터
[도면의 간단한 설명]
제1도는 HIV-LTR에 의한 다수의 TAR요소를 이용하여 HIV유전자 발현을 세포내에서 억제하는 것에 관한 작동가설을 나타낸다.
제2a도는 다수의 TAR요소의 구성 및 전사체의 예상되는 이차 구조를 나타낸다. B. 플라스미드의 일반 구조를 나타낸다.
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (18)

  1. 텐덤하게 전사되도록 적어도 2개의 표적반응요소에 작동적으로 연결되는 프로모터 및 벡터로 이루어진 DNA 구조체.
  2. 제1항에 있어서, 5 내지 50개의 표적반응요소를 가지는 DNA 구조체.
  3. 제2항에 있어서, 25개의 표적반응요소를 가지는 DNA 구조체.
  4. 제1항에 있어서, 상기 반응요소가 활성반응요소인 DNA 구조체.
  5. 제4항에 있어서, 상기 요소가 tat 활성반응요소인 DNA 구조체.
  6. 제1항에 있어서, 상기 프로모터가 바이러스에서 생긴 생성물에 의해 조절가공한 DNA 구조체.
  7. 제6항에 있어서, 상기 프로모터가 HW-l LTR인 DNA 구조체.
  8. 제6항에 있어서, 상기 벡터가 PCD7인 DNA 구조체.
  9. 제1항에 있어서, 바이러스성 RNA에 특이한 리보짐을 코오드화하는 DNA 단편을 더 포함하는 DNA 구조체.
  10. 제1항에 있어서, 전이지배 네가티브 돌연변이 바이러스성 단백질을 코오드화 하는 DNA단편을 더포함하는 DNA 구조체.
  11. 제10항에 있어서, 상기 단백질이 GAG인 DNA 구조체.
  12. 하나의 표적반응요소에 작동적으로 연결되는 프로모터 및 벡터로 필수적으로 구성되는 DNA 구조체.
  13. (i) 바이러스 감염된 환자로부터 세포를 얻고; (ii) 상기 세포내에 청구범위 제1항 또는 제10항에 의한 구조체를 도입시키고; 그리고 (iii) (ii)단계의 세포를 상기 치료가 실행되는 조건하에서 상기 환자에게 다시 도입시키는 단계로 이루어지는 바이러스성 감염을 치료하는 방법.
  14. 제13항에 있어서, 상기 바이러스가 인간 면역결핍 바이러스(HIV)인 방법.
  15. 제13항에 있어서, 상기 세포가 골수세포 또는 혈액세포인 방법.
  16. 저해가 실행되는 조건하에서 청구범위 제1항 또는 제12항에 의한 상기 구조체를 바이러스에 감염된 세포내에 도입시키는 것으로 이루어진 HlV-1복제를 저해하는 방법.
  17. 제16항에 있어서, 상기 바이러스가 HIV인 방법.
  18. 바이러스로 감염된 세포내에 청구범위 제1항에 의한 구조체를 도입시키고, 여기서 상기 바이러스의 생성물이 상기 요소의 전사를 조절하여 상기 저해를 실행하는 것으로 이루어진 바이러스 복제를 저해하는 방법.
    ※ 참고사항:최초출원 내용에 의하여 공개되는 것임.
KR1019920701696A 1990-01-18 1991-01-16 유전자 발현에 영향을 주는 다수의 표적반응요소를 가진 벡터 KR0148782B1 (ko)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US46740790A 1990-01-18 1990-01-18
US467,407 1990-01-18
US59629990A 1990-10-15 1990-10-15
US596,299 1990-10-15
US596299 1990-10-15
PCT/US1991/000175 WO1991010453A1 (en) 1990-01-18 1991-01-16 Vector with multiple target response elements affecting gene expression
US467407 1999-12-20

Publications (2)

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KR920703118A true KR920703118A (ko) 1992-12-17
KR0148782B1 KR0148782B1 (ko) 1998-08-17

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EP (1) EP0511285A4 (ko)
JP (1) JP2746480B2 (ko)
KR (1) KR0148782B1 (ko)
AU (1) AU642959B2 (ko)
CA (1) CA2074188C (ko)
WO (1) WO1991010453A1 (ko)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
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JP2752788B2 (ja) * 1989-01-23 1998-05-18 カイロン コーポレイション 感染および過剰増殖障害の為の組換え療法
US5871958A (en) * 1989-05-25 1999-02-16 Duke University Mutant rev genes encoding transdominant repressors of HIV replication
US6251675B1 (en) 1989-05-25 2001-06-26 Duke University Methods utilizing mutant rev genes encoding transdominant repressors of HIV replication
US6245560B1 (en) 1990-01-18 2001-06-12 The United States Of America As Represented By The Department Of Health And Human Services Vector with multiple target response elements affecting gene expression
GB9125623D0 (en) * 1991-12-02 1992-01-29 Dynal As Cell modification
GB9206874D0 (en) * 1992-03-30 1992-05-13 Connaught Lab Generation of improved inducible mammalian expression vectors
US6469158B1 (en) 1992-05-14 2002-10-22 Ribozyme Pharmaceuticals, Incorporated Synthesis, deprotection, analysis and purification of RNA and ribozymes
US5686599A (en) * 1992-05-14 1997-11-11 Ribozyme Pharmaceuticals, Inc. Synthesis, deprotection, analysis and purification of RNA and ribozymes
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US5693535A (en) * 1992-05-14 1997-12-02 Ribozyme Pharmaceuticals, Inc. HIV targeted ribozymes
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US5654398A (en) * 1993-06-03 1997-08-05 The Regents Of The University Of California Compositions and methods for inhibiting replication of human immunodeficiency virus-1
GB9319772D0 (en) * 1993-09-24 1993-11-10 Therexsys Ltd Therapeutic agent
US5877018A (en) * 1994-10-20 1999-03-02 Connaught Laboratories Limited Synthetic eukaryotic promoters containing two inducible elements
AU702266B2 (en) * 1995-08-25 1999-02-18 Regents Of The University Of California, The Chimeric antiviral agents which incorporate Rev binding nucleic acids
US5891994A (en) 1997-07-11 1999-04-06 Thymon L.L.C. Methods and compositions for impairing multiplication of HIV-1
CN1294631A (zh) * 1998-03-20 2001-05-09 贝尼泰克澳大利亚有限公司 控制基因表达
AU9196798A (en) * 1998-05-04 1999-11-23 Julianna Lisziewicz Chimeric decoy rnas having synergistic anti-hiv activity
US6399067B1 (en) 2000-04-28 2002-06-04 Thymon L.L.C. Methods and compositions for impairing multiplication of HIV-1
WO2006088740A2 (en) 2005-02-15 2006-08-24 Thymon, L.L.C. Methods and compositions for impairing multiplication of hiv-1
IT1397569B1 (it) 2009-12-10 2013-01-16 Icgeb Peptidi e loro derivati che inibiscono il rilascio extracellulare della proteina tat di hiv-1 e la replicazione di hiv-1.

Also Published As

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EP0511285A4 (en) 1993-05-26
WO1991010453A1 (en) 1991-07-25
AU642959B2 (en) 1993-11-04
JPH05504255A (ja) 1993-07-08
EP0511285A1 (en) 1992-11-04
AU7074091A (en) 1991-08-05
JP2746480B2 (ja) 1998-05-06
CA2074188A1 (en) 1991-07-19
KR0148782B1 (ko) 1998-08-17
CA2074188C (en) 2004-05-11

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