Coronavirus cis-Acting RNA Elements

被引:77
作者
Madhugiri, R. [1 ]
Fricke, M. [2 ]
Marz, M. [2 ,3 ]
Ziebuhr, J. [1 ]
机构
[1] Justus Liebig Univ Giessen, Inst Med Virol, Giessen, Germany
[2] Friedrich Schiller Univ Jena, Fac Math & Comp Sci, Jena, Germany
[3] FLI Leibniz Inst Age Res, Jena, Germany
来源
ADVANCES IN VIRUS RESEARCH, VOL 96: CORONAVIRUSES | 2016年 / 96卷
基金
英国生物技术与生命科学研究理事会;
关键词
MOUSE HEPATITIS-VIRUS; RESPIRATORY-SYNDROME CORONAVIRUS; DEFECTIVE INTERFERING RNA; 3' UNTRANSLATED REGION; HOST GENE-EXPRESSION; PROTEIN-PROTEIN INTERACTIONS; RIBONUCLEOPROTEIN A1 BINDS; PUTATIVE MOLECULAR SWITCH; REGULATORY SEQUENCE TRS; LENGTH INFECTIOUS CDNA;
D O I
10.1016/bs.aivir.2016.08.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Coronaviruses have exceptionally large RNA genomes of approximately 30 kilobases. Genome replication and transcription is mediated by a multisubunit protein complex comprised of more than a dozen virus-encoded proteins. The protein complex is thought to bind specific cis-acting RNA elements primarily located in the 50- and 30-terminal genome regions and upstream of the open reading frames located in the 30-proximal one-third of the genome. Here, we review our current understanding of coronavirus cis-acting RNA elements, focusing on elements required for genome replication and packaging. Recent bioinformatic, biochemical, and genetic studies suggest a previously unknown level of conservation of cis-acting RNA structures among different coronavirus genera and, in some cases, even beyond genus boundaries. Also, there is increasing evidence to suggest that individual cis-acting elements may be part of higher-order RNA structures involving long-range and dynamic RNA-RNA interactions between RNA structural elements separated by thousands of nucleotides in the viral genome. We discuss the structural and functional features of these cis-acting RNA elements and their specific functions in coronavirus RNA synthesis.
引用
收藏
页码:127 / 163
页数:37
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