Functional consequences of natural sequence variation in the activation domain of HIV-1 Rev

被引:21
作者
Hua, J
Caffrey, JJ
Cullen, BR
机构
[1] DUKE UNIV, MED CTR, HOWARD HUGHES MED INST, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, DEPT GENET, DURHAM, NC 27710 USA
关键词
D O I
10.1006/viro.1996.0439
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Initial infection with an attenuated form of human immunodeficiency virus type 1 (HIV-I) may give rise to some of the rare asymptomatic infections that have been observed. Recently, data have been presented suggesting that a persistent mutation in the essential activation domain of the HIV-I Rev regulatory protein might have contributed to the maintenance of the asymptomatic state in one individual. Here, we have used a range of assays for in vivo Rev function to examine whether natural sequence variation in the normally highly conserved Rev activation domain can indeed affect Rev function. Analysis of five distinct natural sequence variants of the Rev domain demonstrated that each produced a two- to fourfold drop in Rev function when compared to the consensus activation domain sequence. A sixth sequence, reported for the MN isolate of HIV-I, proved entirely inactive. However, resequencing of this region of the MN genome revealed that this isolate actually encodes a consensus Rev activation domain. Overall, these data reveal that even natural sequence variation in the essential Rev activation domain can result in significantly reduced Rev function and suggest that isolates containing such sequence variation are likely to replicate less effectively. (C) 1996 Academic Press, Inc.
引用
收藏
页码:423 / 429
页数:7
相关论文
共 35 条
[1]   SECRETED PLACENTAL ALKALINE-PHOSPHATASE - A POWERFUL NEW QUANTITATIVE INDICATOR OF GENE-EXPRESSION IN EUKARYOTIC CELLS [J].
BERGER, J ;
HAUBER, J ;
HAUBER, R ;
GEIGER, R ;
CULLEN, BR .
GENE, 1988, 66 (01) :1-10
[2]   IDENTIFICATION OF A NOVEL CELLULAR COFACTOR FOR THE REV/REX CLASS OF RETROVIRAL REGULATORY PROTEINS [J].
BOGERD, HP ;
FRIDELL, RA ;
MADORE, S ;
CULLEN, BR .
CELL, 1995, 82 (03) :485-494
[3]   LONG-TERM HIV-1 INFECTION WITHOUT IMMUNOLOGICAL PROGRESSION [J].
BUCHBINDER, SP ;
KATZ, MH ;
HESSOL, NA ;
OMALLEY, PM ;
HOLMBERG, SD .
AIDS, 1994, 8 (08) :1123-1128
[4]   VIROLOGICAL AND IMMUNOLOGICAL CHARACTERIZATION OF LONG-TERM SURVIVORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
CAO, YZ ;
QIN, LM ;
ZHANG, LQ ;
SAFRIT, J ;
HO, DD .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :201-208
[5]   HIV POPULATION-DYNAMICS IN-VIVO - IMPLICATIONS FOR GENETIC-VARIATION, PATHOGENESIS, AND THERAPY [J].
COFFIN, JM .
SCIENCE, 1995, 267 (5197) :483-489
[6]  
Cullen B R, 1995, AIDS, V9 Suppl A, pS19
[7]  
CULLEN BR, 1987, METHOD ENZYMOL, V152, P684
[8]   GENOMIC STRUCTURE OF AN ATTENUATED QUASI-SPECIES OF HIV-1 FROM A BLOOD-TRANSFUSION DONOR AND RECIPIENTS [J].
DEACON, NJ ;
TSYKIN, A ;
SOLOMON, A ;
SMITH, K ;
LUDFORDMENTING, M ;
HOOKER, DJ ;
MCPHEE, DA ;
GREENWAY, AL ;
ELLETT, A ;
CHATFIELD, C ;
LAWSON, VA ;
CROWE, S ;
MAERZ, A ;
SONZA, S ;
LEARMONT, J ;
SULLIVAN, JS ;
CUNNINGHAM, A ;
DWYER, D ;
DOWTON, D ;
MILLS, J .
SCIENCE, 1995, 270 (5238) :988-991
[9]   ISOLATION AND PARTIAL CHARACTERIZATION OF AN UNUSUAL HUMAN IMMUNODEFICIENCY RETROVIRUS FROM 2 PERSONS OF WEST-CENTRAL AFRICAN ORIGIN [J].
DELEYS, R ;
VANDERBORGHT, B ;
VANDENHAESEVELDE, M ;
HEYNDRICKX, L ;
VANGEEL, A ;
WAUTERS, C ;
BERNAERTS, R ;
SAMAN, E ;
NIJS, P ;
WILLEMS, B ;
TAELMAN, H ;
VANDERGROEN, G ;
PIOT, P ;
TERSMETTE, T ;
HUISMAN, JG ;
VANHEUVERSWYN, H .
JOURNAL OF VIROLOGY, 1990, 64 (03) :1207-1216
[10]   REV PROTEIN OF HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 AFFECTS THE STABILITY AND TRANSPORT OF THE VIRAL MESSENGER-RNA [J].
FELBER, BK ;
HADZOPOULOUCLADARAS, M ;
CLADARAS, C ;
COPELAND, T ;
PAVLAKIS, GN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (05) :1495-1499