Mechanism of minus strand strong stop transfer in HIV-1 reverse transcription

被引:32
作者
Chen, Y
Balakrishnan, M
Roques, BP
Fay, PJ
Bambara, RA
机构
[1] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Ctr Canc, Rochester, NY 14642 USA
[3] CNRS, UER Sci Pharmaceut & Biol, URA D1500, U266,INSERM,Dept Pharmacochim Mol & Struct, F-75270 Paris, France
关键词
D O I
10.1074/jbc.M210959200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Retrovirus minus strand strong stop transfer (minus strand transfer) requires reverse transcriptase-associated RNase H, R sequence homology, and viral nucleocapsid protein. The minus strand transfer mechanism in human immunodeficiency virus-1 was examined in vitro with purified protein and substrates. Blocking donor RNA 5'-end cleavage inhibited transfers when template homology was 19 nucleotides (nt) or less. Cleavage of the donor W-end occurred prior to formation of transfer products. This suggests that when template homology is short, transfer occurs through a primer terminus switch-initiated mechanism, which requires cleavage of the donor 5' terminus. On templates with 26-nt and longer homology, transfer occurred before cleavage of the donor 5' terminus. Transfer was unaffected when donor 5'-end cleavages were blocked but was reduced when internal cleavages within the donor were restricted. Based on the overall data, we conclude that in human immunodeficiency virus-1, which contains a 97-nt R sequence, minus strand transfer occurs through an acceptor invasion-initiated mechanism. Transfer is initiated at internal regions of the homologous R sequence without requiring cleavage at the donor W-end. The acceptor invades at gaps created by reverse transcriptase-RNase H in the donor-cDNA hybrid. The fragmented donor is eventually strand-displaced by the acceptor, completing the transfer.
引用
收藏
页码:8006 / 8017
页数:12
相关论文
共 80 条
[61]   Structural determinants of murine leukemia virus reverse transcriptase that affect the frequency of template switching [J].
Svarovskaia, ES ;
Delviks, KA ;
Hwang, CK ;
Pathak, VK .
JOURNAL OF VIROLOGY, 2000, 74 (15) :7171-7178
[62]   ABORTIVE REVERSE TRANSCRIPTION BY MUTANTS OF MOLONEY MURINE LEUKEMIA-VIRUS DEFICIENT IN THE REVERSE TRANSCRIPTASE-ASSOCIATED RNASE H-FUNCTION [J].
TANESE, N ;
TELESNITSKY, A ;
GOFF, SP .
JOURNAL OF VIROLOGY, 1991, 65 (08) :4387-4397
[63]   DEFECTS IN MOLONEY MURINE LEUKEMIA-VIRUS REPLICATION CAUSED BY A REVERSE-TRANSCRIPTASE MUTATION MODELED ON THE STRUCTURE OF ESCHERICHIA-COLI RNASE-H [J].
TELESNITSKY, A ;
BLAIN, SW ;
GOFF, SP .
JOURNAL OF VIROLOGY, 1992, 66 (02) :615-622
[64]  
Telesnitsky A., 1997, P121
[65]  
Telesnitsky A., 1993, REVERSE TRANSCRIPTAS, P49
[66]   Cis-acting elements required for strong stop acceptor template selection during Moloney murine leukemia virus reverse transcription [J].
Topping, R ;
Demoitie, MA ;
Shin, NH ;
Telesnitsky, A .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 281 (01) :1-15
[67]   DNA STRAND EXCHANGE AND SELECTIVE DNA ANNEALING PROMOTED BY THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 NUCLEOCAPSID PROTEIN [J].
TSUCHIHASHI, Z ;
BROWN, PO .
JOURNAL OF VIROLOGY, 1994, 68 (09) :5863-5870
[68]   KINETICS OF SYNTHESIS, STRUCTURE AND PURIFICATION OF AVIAN-SARCOMA VIRUS-SPECIFIC DNA MADE IN CYTOPLASM OF ACUTELY INFECTED-CELLS [J].
VARMUS, HE ;
HEASLEY, S ;
KUNG, HJ ;
OPPERMANN, H ;
SMITH, VC ;
BISHOP, JM ;
SHANK, PR .
JOURNAL OF MOLECULAR BIOLOGY, 1978, 120 (01) :55-82
[69]  
Vogt V. M., 1997, P27
[70]   Requirements for minus-strand transfer catalyzed by Rous sarcoma virus reverse transcriptase [J].
Werner, S ;
Vogel-Bachmayr, K ;
Hollinderbäumer, B ;
Wöhrl, BM .
JOURNAL OF VIROLOGY, 2001, 75 (21) :10132-10138