An RNA tertiary structure in the 3' untranslated region of enteroviruses is necessary for efficient replication

被引:78
作者
Mirmomeni, MH [1 ]
Hughes, PJ [1 ]
Stanway, G [1 ]
机构
[1] UNIV ESSEX, JOHN TABOR LABS, DEPT CHEM & BIOL SCI, COLCHESTER CO4 3SQ, ESSEX, ENGLAND
关键词
D O I
10.1128/JVI.71.3.2363-2370.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
RNA tertiary structures, such as pseudoknots, are known to be biologically significant in a number of virus systems, The 3' untranslated regions of the RNA genomes of all members of the Enterovirus genus of Picornaviridae exhibit a potential, pseudoknot-like, tertiary structure interaction of an unusual type, This is formed by base pairing between loop regions of two secondary structure domains, It is distinct from a potential, conventional pseudoknot, studied previously in poliovirus, which is less conserved phylogenetically. We have analyzed the tertiary structure feature in one enterovirus, coxsackievirus A9, using specific mutagenesis. A double mutant in which the potential interaction was destroyed was nonviable, and viability was restored by introducing compensating mutations, predicted to allow the interaction to reform, Phenotypic pseudorevertants of virus mutants, having mutations designed to disrupt the interaction, were all found to have acquired nucleotide changes which restored the potential interaction. Analysis of one mutant containing a single-base mutation indicated a greatly increased temperature sensitivity due to a step early in replication. The results show that, in addition to secondary structures, tertiary RNA structural interactions can play an important role in the biology of picornaviruses.
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收藏
页码:2363 / 2370
页数:8
相关论文
共 33 条
[1]   POLIOVIRUS RNA-SYNTHESIS UTILIZES AN RNP COMPLEX FORMED AROUND THE 5'-END OF VIRAL-RNA [J].
ANDINO, R ;
RIECKHOF, GE ;
ACHACOSO, PL ;
BALTIMORE, D .
EMBO JOURNAL, 1993, 12 (09) :3587-3598
[2]   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
[3]   THE NUCLEOTIDE-SEQUENCE OF COXSACKIEVIRUS-A9 - IMPLICATIONS FOR RECEPTOR-BINDING AND ENTEROVIRUS CLASSIFICATION [J].
CHANG, KH ;
AUVINEN, P ;
HYYPIA, T ;
STANWAY, G .
JOURNAL OF GENERAL VIROLOGY, 1989, 70 :3269-3280
[4]   LOCALIZATION OF BINDING-SITE FOR ENCEPHALOMYOCARDITIS VIRUS-RNA POLYMERASE IN THE 3'-NONCODING REGION OF THE VIRAL-RNA [J].
CUI, T ;
PORTER, AG .
NUCLEIC ACIDS RESEARCH, 1995, 23 (03) :377-382
[5]   RNA PSEUDOKNOT DOMAIN OF TOBACCO MOSAIC-VIRUS CAN FUNCTIONALLY SUBSTITUTE FOR A POLY(A) TAIL IN PLANT AND ANIMAL-CELLS [J].
GALLIE, DR ;
WALBOT, V .
GENES & DEVELOPMENT, 1990, 4 (07) :1149-1157
[6]   AMPLIFICATION OF RHINOVIRUS SPECIFIC NUCLEIC-ACIDS FROM CLINICAL-SAMPLES USING THE POLYMERASE CHAIN-REACTION [J].
GAMA, RE ;
HORSNELL, PR ;
HUGHES, PJ ;
NORTH, C ;
BRUCE, CB ;
ALNAKIB, W ;
STANWAY, G .
JOURNAL OF MEDICAL VIROLOGY, 1989, 28 (02) :73-77
[7]  
HARRIS KS, 1994, J BIOL CHEM, V269, P27004
[8]   AN UNUSUAL RNA TERTIARY INTERACTION HAS A ROLE FOR THE SPECIFIC AMINOACYLATION OF A TRANSFER-RNA [J].
HOU, YM ;
WESTHOF, E ;
GIEGE, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) :6776-6780
[9]   THE COXSACKIEVIRUS A9 RGD MOTIF IS NOT ESSENTIAL FOR VIRUS VIABILITY [J].
HUGHES, PJ ;
HORSNELL, C ;
HYYPIA, T ;
STANWAY, G .
JOURNAL OF VIROLOGY, 1995, 69 (12) :8035-8040
[10]   BIOLOGY OF COXSACKIE-A VIRUSES [J].
HYYPIA, T ;
STANWAY, G .
ADVANCES IN VIRUS RESEARCH, VOL 42, 1993, 42 :343-373