Evidence for a unique mechanism of strand transfer from the transactivation response region of HIV-1

被引:97
作者
Kim, JK
Palaniappan, C
Wu, WM
Fay, PJ
Bambara, RA
机构
[1] UNIV ROCHESTER,MED CTR,DEPT BIOCHEM & BIOPHYS,ROCHESTER,NY 14642
[2] UNIV ROCHESTER,DEPT MED,ROCHESTER,NY 14642
[3] UNIV ROCHESTER,CTR CANC,ROCHESTER,NY 14642
关键词
D O I
10.1074/jbc.272.27.16769
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
We previously found that strand transfer by human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) is promoted at sites where RT pauses during synthesis, In this report, strand transfer is measured within the 5' transactivation response region (TAR) of HIV-1 RNA, We hypothesized that the stable hairpin structure of TAR would induce RT pausing, promoting RNase II-directed cleavage of the template and subsequent transfer at that site, We further predicted that HIV-1 nucleocapsid protein (NC), known to melt secondary structures, would decrease transfer, We show that TAR created a strong pause site for RT, but NC significantly promoted strand transfer, The effect of NC is specific, since other single strand binding proteins failed to stimulate transfer, In another unexpected outcome, preferred positions of internal transfer were not at the pause site but were in the upper stem and loop of TAR, Thus, we propose a new mechanism for transfer within TAR described by an interactive hairpin model, in which association between the donor and the acceptor templates within the TAR stem promotes transfer, The model is consistent with the observed stimulation of strand transfer by NC, The model is applicable to internal and replicative end transfer.
引用
收藏
页码:16769 / 16777
页数:9
相关论文
共 36 条
[1]   PAUSING BY RETROVIRAL DNA-POLYMERASES PROMOTES STRAND TRANSFER FROM INTERNAL REGIONS OF RNA DONOR TEMPLATES TO HOMOPOLYMERIC ACCEPTOR TEMPLATES [J].
BUISER, RG ;
BAMBARA, RA ;
FAY, PJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1216 (01) :20-30
[2]   STRUCTURE, REPLICATION, AND RECOMBINATION OF RETROVIRUS GENOMES - SOME UNIFYING HYPOTHESES [J].
COFFIN, JM .
JOURNAL OF GENERAL VIROLOGY, 1979, 42 (JAN) :1-26
[3]   TRANSACTIVATION OF HUMAN-IMMUNODEFICIENCY-VIRUS OCCURS VIA A BIMODAL MECHANISM [J].
CULLEN, BR .
CELL, 1986, 46 (07) :973-982
[4]   VIRAL-RNA ANNEALING ACTIVITIES OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 NUCLEOCAPSID PROTEIN REQUIRE ONLY PEPTIDE DOMAINS OUTSIDE THE ZINC FINGERS [J].
DEROCQUIGNY, H ;
GABUS, C ;
VINCENT, A ;
FOURNIEZALUSKI, MC ;
ROQUES, B ;
DARLIX, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6472-6476
[5]  
DESTEFANO JJ, 1994, J BIOL CHEM, V269, P161
[6]   REQUIREMENTS FOR STRAND TRANSFER BETWEEN INTERNAL REGIONS OF HETEROPOLYMER TEMPLATES BY HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE [J].
DESTEFANO, JJ ;
MALLABER, LM ;
RODRIGUEZRODRIGUEZ, L ;
FAY, PJ ;
BAMBARA, RA .
JOURNAL OF VIROLOGY, 1992, 66 (11) :6370-6378
[7]   PARAMETERS THAT INFLUENCE PROCESSIVE SYNTHESIS AND SITE-SPECIFIC TERMINATION BY HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE ON RNA AND DNA TEMPLATES [J].
DESTEFANO, JJ ;
BUISER, RG ;
MALLABER, LM ;
FAY, PJ ;
BAMBARA, RA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1131 (03) :270-280
[8]   HUMAN IMMUNODEFICIENCY VIRUS-1 TAT PROTEIN BINDS TRANS-ACTIVATION-RESPONSIVE REGION (TAR) RNA INVITRO [J].
DINGWALL, C ;
ERNBERG, I ;
GAIT, MJ ;
GREEN, SM ;
HEAPHY, S ;
KARN, J ;
LOWE, AD ;
SINGH, M ;
SKINNER, MA ;
VALERIO, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :6925-6929
[9]   Helix structure and ends of RNA/DNA hybrids direct the cleavage specificity of HIV-1 reverse transcriptase RNase H [J].
Palaniappan, C ;
Fuentes, GM ;
RodriguezRodriguez, L ;
Fay, PJ ;
Bambara, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (04) :2063-2070
[10]   DETAILED MODEL OF REVERSE TRANSCRIPTION AND TESTS OF CRUCIAL ASPECTS [J].
GILBOA, E ;
MITRA, SW ;
GOFF, S ;
BALTIMORE, D .
CELL, 1979, 18 (01) :93-100