A coding RNA sequence acts as a replication signal in cardioviruses

被引:100
作者
Lobert, PE
Escriou, N
Ruelle, J
Michiels, T
机构
[1] Catholic Univ Louvain, Christian de Duve Inst Cellular Pathol, Microbial Pathogenesis Unit, MIPA,VIRO 7479, B-1020 Brussels, Belgium
[2] Inst Pasteur, Unite Genet Mol Virus Respunivir, CNRS, URA 1966, F-75724 Paris 15, France
关键词
D O I
10.1073/pnas.96.20.11560
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Theiler's virus and Mengo virus are representatives of the Cardiovirus genus within the picornavirus family, Their genome is an 8-kilobase long positive strand RNA molecule. This RNA molecule plays three roles in infected cells: It serves as a messenger RNA, acts as a template for genome replication, and is encapsidated to form progeny virions. We observed that a cis-acting signal required for replication of Theiler's virus was contained within a 130-nt stretch of the region encoding the capsid protein VP2. This RNA sequence does not influence internal ribosome entry site-mediated translation initiation and thus likely acts directly as a signal for the replication complex. We found a similar signal in the VP2-coding sequence of Mengo virus, and both signals could be functionally exchanged. Within the replication element, a 9-nt sequence that is highly conserved among cardioviruses was shown to be essential for replication. This conserved sequence was contained in mostly unpaired regions of the RNA secondary structure predicted for the replication elements of the various cardioviruses. Interestingly, a similar replication element has been reported to occur in the distantly related human rhinovirus type 14, suggesting that such elements could be conserved throughout the picornavirus family. However, the different location of the replication elements in rhinovirus and cardioviruses, and the fact that they were not functionally exchangeable, is raising intriguing questions about the evolution of such signals in picornaviruses.
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页码:11560 / 11565
页数:6
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