Viral and Cellular mRNA Translation in Coronavirus-Infected Cells.
Viral and Cellular mRNA Translation in Coronavirus-Infected Cells.
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冠状病毒感染细胞中的病毒和细胞mRNA翻译。
DOI:
10.1016/bs.aivir.2016.08.001
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发表时间:
2016
影响因子:
--
通讯作者:
Makino S
中科院分区:
文献类型:
--
作者:
Nakagawa K;Lokugamage KG;Makino S
Coronaviruses have large positive-strand RNA genomes that are 5′ capped and 3′ polyadenylated. The 5′-terminal two-thirds of the genome contain two open reading frames (ORFs), 1a and 1b, that together make up the viral replicase gene and encode two large polyproteins that are processed by viral proteases into 15–16 nonstructural proteins, most of them being involved in viral RNA synthesis. ORFs located in the 3′-terminal one-third of the genome encode structural and accessory proteins and are expressed from a set of 5′ leader-containing subgenomic mRNAs that are synthesized by a process called discontinuous transcription. Coronavirus protein synthesis not only involves cap-dependent translation mechanisms but also employs regulatory mechanisms, such as ribosomal frameshifting. Coronavirus replication is known to affect cellular translation, involving activation of stress-induced signaling pathways, and employing viral proteins that affect cellular mRNA translation and RNA stability. This chapter describes our current understanding of the mechanisms involved in coronavirus mRNA translation and changes in host mRNA translation observed in coronavirus-infected cells.