ADENOASSOCIATED VIRUS (AAV) REP PROTEINS MEDIATE COMPLEX-FORMATION BETWEEN AAV DNA AND ITS INTEGRATION SITE IN HUMAN DNA

被引:294
作者
WEITZMAN, MD
KYOSTIO, SRM
KOTIN, RM
OWENS, RA
机构
[1] NIDDKD,MOLEC & CELLULAR BIOL LAB,BETHESDA,MD 20892
[2] NHLBI,MOLEC HEMATOL BRANCH,BETHESDA,MD 20892
[3] GENET THERAPY INC,GAITHERSBURG,MD 20878
关键词
D O I
10.1073/pnas.91.13.5808
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
AAV is unique among eukaryotic viruses in the ability of its DNA to integrate preferentially into a specific region of the human genome. Understanding AAV integration may aid in developing gene therapy systems with predictable integration sites. Using a gel mobility-shift assay, we have identified a DNA sequence within the AAV integration locus on human chromosome 19 which is specifically bound by the AAV Rep78 and Rep68 proteins. This Rep recognition sequence is a GCTC repeating moth very similar to sequences within the inverted terminal repeats of the AAV genome which are also bound by Rep78 and Rep68. Cloned oligonucleotides containing the recognition sequence can direct specific binding by Rep proteins. Binding assays with mutant Rep proteins show that the amino-terminal portion of Rep78 and Rep68 can direct binding to either the AAV terminal repeat hairpin DNA or chromosome 19. This human genomic DNA can be complexed with AAV DNA by Rep proteins as demonstrated by a dual-label (P-32/biotin) assay. These results suggest a role for Rep in targeting viral integration.
引用
收藏
页码:5808 / 5812
页数:5
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