Viral subversion of the host protein synthesis machinery

被引:410
作者
Walsh, Derek [1 ,3 ]
Mohr, Ian [1 ,2 ]
机构
[1] NYU, Sch Med, Dept Microbiol, New York, NY 10016 USA
[2] NYU, Sch Med, Inst Canc, New York, NY 10016 USA
[3] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin 9, Ireland
基金
爱尔兰科学基金会; 美国国家卫生研究院;
关键词
EUKARYOTIC TRANSLATION INITIATION; RIBOSOME ENTRY SITE; MESSENGER-RNA TRANSLATION; VESICULAR STOMATITIS-VIRUS; GENOME-LINKED PROTEIN; HEPATITIS-C; VACCINIA VIRUS; STRESS GRANULES; BINDING-PROTEIN; P-BODIES;
D O I
10.1038/nrmicro2655
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viruses are fully reliant on the translation machinery of their host cells to produce the polypeptides that are essential for viral replication. Consequently, viruses recruit host ribosomes to translate viral mRNAs, typically using virally encoded functions to seize control of cellular translation factors and the host signalling pathways that regulate their activity. This not only ensures that viral proteins will be produced, but also stifles innate host defences that are aimed at inhibiting the capacity of infected cells for protein synthesis. Remarkably, nearly every step of the translation process can be targeted by virally encoded functions. This Review discusses the diverse strategies that viruses use to subvert host protein synthesis functions and regulate mRNA translation in infected cells.
引用
收藏
页码:860 / 875
页数:16
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