SITE-SPECIFIC INTEGRATION BY ADENOASSOCIATED VIRUS IS DIRECTED BY A CELLULAR DNA-SEQUENCE

被引:124
作者
GIRAUD, C
WINOCOUR, E
BERNS, KI
机构
[1] CORNELL UNIV,COLL MED,HEARST MICROBIOL RES CTR,DEPT MICROBIOL,NEW YORK,NY 10021
[2] WEIZMANN INST SCI,DEPT MOLEC GENET & VIROL,IL-76100 REHOVOT,ISRAEL
关键词
D O I
10.1073/pnas.91.21.10039
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Different regions of an 8.2-kb cloned DNA segment containing the target for adeno-associated virus (AAV) integration in human chromosome 19q13.3-qter (AAVS1 locus) were subcloned in an Epstein-Barr virus-based shuttle vector and propagated as episomes in a derivative of the 293 human embryonic kidney cell line. Preferential recombination with an infecting AAV genome was assessed by measuring the frequency of recombinants among the shuttle vectors recovered in Escherichia coli. The signals which direct recombination with the AAV genome were localized to a 510-nt region at the 5' end of the 8.2-kb AAVS1 DNA. Hence, the results indicate that site-specific integration of AAV is directed by a specific DNA sequence on human chromosome 19. An unusual degree of DNA heterogeneity in the recovered vector was also associated with the 510 nt at the 5' end of AAVS1 DNA, suggesting that the AAV chromosomal integration locus may be involved in genomic instability.
引用
收藏
页码:10039 / 10043
页数:5
相关论文
共 33 条
[1]   IDENTIFICATION OF NUCLEAR PROTEINS THAT SPECIFICALLY INTERACT WITH ADENO-ASSOCIATED VIRUS TYPE-2 INVERTED TERMINAL REPEAT HAIRPIN DNA [J].
ASHKTORAB, H ;
SRIVASTAVA, A .
JOURNAL OF VIROLOGY, 1989, 63 (07) :3034-3039
[2]   PARVOVIRUS REPLICATION [J].
BERNS, KI .
MICROBIOLOGICAL REVIEWS, 1990, 54 (03) :316-329
[3]   OUABAIN-RESISTANT MUTANTS OF THE RAT NA,K-ATPASE ALPHA-2 ISOFORM IDENTIFIED BY USING AN EPISOMAL EXPRESSION VECTOR [J].
CANFIELD, V ;
EMANUEL, JR ;
SPICKOFSKY, N ;
LEVENSON, R ;
MARGOLSKEE, RF .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (04) :1367-1372
[4]  
CHORINI JA, 1994, J VIROL, V68, P797
[5]   ANALYSIS OF MUTATION IN HUMAN-CELLS BY USING AN EPSTEIN-BARR-VIRUS SHUTTLE SYSTEM [J].
DUBRIDGE, RB ;
TANG, P ;
HSIA, HC ;
LEONG, PM ;
MILLER, JH ;
CALOS, MP .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (01) :379-387
[6]   LIPOFECTION - A HIGHLY EFFICIENT, LIPID-MEDIATED DNA-TRANSFECTION PROCEDURE [J].
FELGNER, PL ;
GADEK, TR ;
HOLM, M ;
ROMAN, R ;
CHAN, HW ;
WENZ, M ;
NORTHROP, JP ;
RINGOLD, GM ;
DANIELSEN, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7413-7417
[7]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467
[8]  
Greener A., 1990, STRATEGIES MOL BIOL, V3, P5
[10]   PARTIAL-PURIFICATION OF ADENOASSOCIATED VIRUS REP78, REP52, AND REP40 AND THEIR BIOCHEMICAL-CHARACTERIZATION [J].
IM, DS ;
MUZYCZKA, N .
JOURNAL OF VIROLOGY, 1992, 66 (02) :1119-1128