The frameshift stimulatory signal of human immunodeficiency virus type 1 group O is a pseudoknot

被引:33
作者
Baril, M [1 ]
Dulude, D [1 ]
Steinberg, SV [1 ]
Brakier-Gingras, L [1 ]
机构
[1] Univ Montreal, Dept Biochim, Montreal, PQ H3T 1J4, Canada
关键词
human immunodeficiency virus type 1; HIV-1 group O; ribosomal frameshiffing; RNA structure; RNA pseudoknot;
D O I
10.1016/S0022-2836(03)00784-8
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
Human immunodeficiency virus type 1 (HIV-1) requires a programmed-1 ribosomal frameshift to produce Gag-Pol, the precursor of its enzymatic activities. This frameshift occurs at a slippery sequence on the viral messenger RNA and is stimulated by a specific structure, downstream of the shift site. While in group M, the most abundant HIV-1 group, the frameshift stimulatory signal is an extended bulged stem-loop, we show here, using a combination of mutagenesis and probing studies, that it is a pseudoknot in group O. The mutagenesis and probing studies coupled to an in silico analysis show that group O pseudoknot is a hairpin-type pseudoknot with two coaxially stacked stems of eight base-pairs (stem 1 and stem 2), connected by single-stranded loops of 2 nt (loop 1) and 20 nt (loop 2). Mutations impairing formation of stem 1 or stem 2 of the pseudoknot reduce frameshift efficiency, whereas compensatory changes that allow re-formation of these stems restore the frameshift efficiency to near wild-type level. The difference between the frameshift stimulatory signal of group O and group M supports the hypothesis that these groups originate from a different monkey to human transmission. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:571 / 583
页数:13
相关论文
共 44 条
[1]  
*AL NAT LAB, 2002, HUM RETR AIDS ED
[2]   MUTATIONAL ANALYSIS OF THE RNA PSEUDOKNOT COMPONENT OF A CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL [J].
BRIERLEY, I ;
ROLLEY, NJ ;
JENNER, AJ ;
INGLIS, SC .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 220 (04) :889-902
[3]   CHARACTERIZATION OF AN EFFICIENT CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL - REQUIREMENT FOR AN RNA PSEUDOKNOT [J].
BRIERLEY, I ;
DIGARD, P ;
INGLIS, SC .
CELL, 1989, 57 (04) :537-547
[4]   RIBOSOMAL FRAMESHIFTING ON VIRAL RNAS [J].
BRIERLEY, I .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :1885-1892
[5]  
BRIERLEY I, 2001, RIBOSOME, P233
[6]   AN RNA PSEUDOKNOT AND AN OPTIMAL HEPTAMERIC SHIFT SITE ARE REQUIRED FOR HIGHLY EFFICIENT RIBOSOMAL FRAMESHIFTING ON A RETROVIRAL MESSENGER-RNA [J].
CHAMORRO, M ;
PARKIN, N ;
VARMUS, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (02) :713-717
[7]   A characteristic bent conformation of RNA pseudoknots promotes -1 frameshifting during translation of retroviral RNA [J].
Chen, XY ;
Kang, HS ;
Shen, LX ;
Chamorro, M ;
Varmus, HE ;
Tinoco, I .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 260 (04) :479-483
[8]   Natural residues versus antiretroviral drug-selected mutations in HIV type 1 group O reverse transcriptase and protease related to virological drug failure in vivo [J].
de Baar, MP ;
Janssens, W ;
de Ronde, A ;
Fransen, K ;
Colebunders, R ;
Kestens, L ;
van der Groen, G ;
Goudsmit, J .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2000, 16 (14) :1385-1394
[9]   The late domain of human immunodeficiency virus type 1 p6 promotes virus release in a cell type-dependent manner [J].
Demirov, DG ;
Orenstein, JM ;
Freed, EO .
JOURNAL OF VIROLOGY, 2002, 76 (01) :105-117
[10]   Susceptibility of human immunodeficiency virus type 1 group O isolates to antiretroviral agents: In vitro phenotypic and genotypic analyses [J].
Descamps, D ;
Collin, G ;
Letourneur, F ;
Apetrei, C ;
Damond, F ;
LoussertAjaka, I ;
Simon, F ;
Saragosti, S ;
BrunVezinet, F .
JOURNAL OF VIROLOGY, 1997, 71 (11) :8893-8898