A distinct group of hepacivirus/pestivirus-like internal ribosomal entry sites in members of diverse Picornavirus genera:: Evidence for modular exchange of functional noncoding RNA elements by recombination

被引:116
作者
Hellen, Christopher U. T. [1 ]
de Breyne, Sylvain [1 ]
机构
[1] Suny Downstate Med Ctr, Dept Immunol & Microbiol, Brooklyn, NY 11203 USA
关键词
D O I
10.1128/JVI.02403-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The 5' untranslated regions (UTRs) of the RNA genomes of Flaviviridae of the Hepacivirus and Pestivirus genera contain internal ribosomal entry sites (IRESs) that are unrelated to the two principal classes of IRESs of Picornaviridae. The mechanism of translation initiation on hepacivirus/pestivirus (HP) IRESs, which involves factor-independent binding to ribosomal 40S subunits, also differs fundamentally from initiation on these picornavirus IRESs. Ribosomal binding to HP IRESs requires conserved sequences that form a pseudoknot and the adjacent IIId and IIIe domains; analogous elements do not occur in the two principal groups of picornavirus IRESs. Here, comparative sequence analysis was used to identify a subset of picornaviruses from multiple genera that contain 5' UTR sequences with significant similarities to HP IRESs. They are avian encephallomyelitis virus, duck hepatitis virus 1, duck picornavirus, porcine teschovirus, porcine enterovirus 8, Seneca Valley virus, and simian picornavirus. Their 5' UTRs are predicted to form several structures, in some of which the peripheral elements differ from the corresponding HP IRES elements but in which the core pseudoknot, domain IIId, and domain IIIe elements are all closely related. These findings suggest that HP-like IRESs have been exchanged between unrelated virus families by recombination and support the hypothesis that RNA viruses consist of modular coding and noncoding elements that can exchange and evolve independently.
引用
收藏
页码:5850 / 5863
页数:14
相关论文
共 75 条
[1]   SECONDARY STRUCTURE OF THE 5' NONTRANSLATED REGIONS OF HEPATITIS-C VIRUS AND PESTIVIRUS GENOMIC RNAS [J].
BROWN, EA ;
ZHANG, HC ;
PING, LH ;
LEMON, SM .
NUCLEIC ACIDS RESEARCH, 1992, 20 (19) :5041-5045
[2]   Hepatitis C virus-related internal ribosome entry sites are found in multiple genera of the family Picornaviridae [J].
Chard, LS ;
Bordeleau, ME ;
Pelletier, J ;
Tanaka, J ;
Belsham, GJ .
JOURNAL OF GENERAL VIROLOGY, 2006, 87 :927-936
[3]   Functional analyses of RNA structures shared between the internal ribosome entry sites of hepatitis C virus and the picornavirus porcine teschovirus 1 Talfan [J].
Chard, LS ;
Kaku, Y ;
Jones, B ;
Nayak, A ;
Belsham, GJ .
JOURNAL OF VIROLOGY, 2006, 80 (03) :1271-1279
[4]   TRANSDUCTION OF A HUMAN RNA SEQUENCE BY POLIOVIRUS [J].
CHARINI, WA ;
TODD, S ;
GUTMAN, GA ;
SEMLER, BL .
JOURNAL OF VIROLOGY, 1994, 68 (10) :6547-6552
[5]   Evaluation of several lightweight stochastic context-free grammars for RNA secondary structure prediction [J].
Dowell, RD ;
Eddy, SR .
BMC BIOINFORMATICS, 2004, 5 (1)
[6]   The influence of viral coding sequences on pestivirus IRES activity reveals further parallels with translation initiation in prokaryotes [J].
Fletcher, SP ;
Ali, IK ;
Kaminski, A ;
Digard, P ;
Jackson, RJ .
RNA, 2002, 8 (12) :1558-1571
[7]   Pestivirus Internal Ribosome Entry Site (IRES) structure and function:: Elements in the 5′ untranslated region important for IRES function [J].
Fletcher, SP ;
Jackson, RJ .
JOURNAL OF VIROLOGY, 2002, 76 (10) :5024-5033
[8]   Sequences in the 5′ nontranslated region of hepatitis C virus required for RNA replication [J].
Friebe, P ;
Lohmann, V ;
Krieger, N ;
Bartenschlager, R .
JOURNAL OF VIROLOGY, 2001, 75 (24) :12047-12057
[9]   Cis-acting RNA elements required for replication of bovine viral diarrhea virus hepatitis C virus 5′ nontranslated region chimeras [J].
Frolov, I ;
McBride, MS ;
Rice, CM .
RNA, 1998, 4 (11) :1418-1435
[10]   Hepatitis C virus and the related bovine viral diarrhea virus considerably differ in the functional organization of the 5′ non-translated region:: Implications for the viral life cycle [J].
Grassmann, CW ;
Yu, HY ;
Isken, O ;
Behrens, SE .
VIROLOGY, 2005, 333 (02) :349-366