The 5′-terminal region of the Aichi virus genome encodes cis-acting replication elements required for positive- and negative-strand RNA synthesis

被引:27
作者
Nagashima, S [1 ]
Sasaki, J [1 ]
Taniguchi, K [1 ]
机构
[1] Fujita Hlth Univ, Sch Med, Dept Virol & Parasitol, Toyoake, Aichi 4701192, Japan
关键词
D O I
10.1128/JVI.79.11.6918-6931.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aichi virus is a member of the family Picornaviridae. It has already been shown that three stem-loop structures (SL-A, SL-B, and SL-C, from the 5' end) formed at the 5' end of the genome are critical elements for viral RNA replication. In this study, we further characterized the 5'-terminal cis-acting replication elements. We found that an additional structural element, a pseudoknot structure, is formed through base-pairing interaction between the loop segment of SL-B (nucleotides [nt] 57 to 60) and a sequence downstream of SL-C (nt 112 to 115) and showed that the formation of this pseudoknot is critical for viral RNA replication. Mapping of the 5'-terminal sequence of the Aichi virus genome required for RNA replication using a series of Aichi virus-encephalomyocarditis virus chimera replicons indicated that the 5'-end 115 nucleotides including the pseudoknot structure are the minimum requirement for RNA replication. Using the cell-free translation-replication system, we examined the abilities of viral RNAs with a lethal mutation in the 5'-terminal structural elements to synthesize negative- and positive-strand RNAs. The results showed that the formation of three stem-loops and the pseudoknot structure at the 5' end of the genome is required for negative-strand RNA synthesis. In addition, specific nucleotide sequences in the stem of SL-A or its complementary sequences at the 3' end of the negative-strand were shown to be critical for the initiation of positive-strand RNA synthesis but not for that of negative-strand synthesis. Thus, the 5' end of the Aichi virus genome encodes elements important for not only negative-strand synthesis but also positive-strand synthesis.
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页码:6918 / 6931
页数:14
相关论文
共 51 条
[1]   POLIOVIRUSES CONTAINING PICORNAVIRUS TYPE-1 AND/OR TYPE-2 INTERNAL RIBOSOMAL ENTRY SITE ELEMENTS - GENETIC HYBRIDS AND THE EXPRESSION OF A FOREIGN GENE [J].
ALEXANDER, L ;
LU, HH ;
WIMMER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1406-1410
[2]   A FUNCTIONAL RIBONUCLEOPROTEIN COMPLEX FORMS AROUND THE 5' END OF POLIOVIRUS RNA [J].
ANDINO, R ;
RIECKHOF, GE ;
BALTIMORE, D .
CELL, 1990, 63 (02) :369-380
[3]   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
[4]  
Bartlett MG, 1996, J MASS SPECTROM, V31, P275, DOI 10.1002/(SICI)1096-9888(199603)31:3<275::AID-JMS294>3.0.CO
[5]  
2-Q
[6]   Translating ribosomes inhibit poliovirus negative-strand RNA synthesis [J].
Barton, DJ ;
Morasco, BJ ;
Flanegan, JB .
JOURNAL OF VIROLOGY, 1999, 73 (12) :10104-10112
[7]   COMPLETE REPLICATION OF POLIOVIRUS IN-VITRO - PREINITIATION RNA REPLICATION COMPLEXES REQUIRE SOLUBLE CELLULAR FACTORS FOR THE SYNTHESIS OF VPG-LINKED RNA [J].
BARTON, DJ ;
BLACK, EP ;
FLANEGAN, JB .
JOURNAL OF VIROLOGY, 1995, 69 (09) :5516-5527
[8]   5′ cloverleaf in poliovirus RNA is a cis-acting replication element required for negative-strand synthesis [J].
Barton, DJ ;
O'Donnell, BJ ;
Flanegan, JB .
EMBO JOURNAL, 2001, 20 (06) :1439-1448
[9]   The structure, function and application of the hammerhead ribozyme [J].
Birikh, KR ;
Heaton, PA ;
Eckstein, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 245 (01) :1-16
[10]   Cell-dependent role for the poliovirus 3′ noncoding region in positive-strand RNA synthesis [J].
Brown, DM ;
Kauder, SE ;
Cornell, CT ;
Jang, GM ;
Racaniello, VR ;
Semler, BL .
JOURNAL OF VIROLOGY, 2004, 78 (03) :1344-1351