Battling for Ribosomes: Translational Control at the Forefront of the Antiviral Response

被引:29
|
作者
Hoang, Huy-Dung [1 ,2 ]
Graber, Tyson E. [2 ]
Alain, Tommy [1 ,2 ]
机构
[1] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Childrens Hosp, Eastern Ontario Res Inst, Ottawa, ON K1H 8L1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Virus; mTOR; protein synthesis; stress granules; ribosome profiling; ACTIVATED PROTEIN-KINASE; STRANDED-RNA BINDING; STRESS GRANULE FORMATION; FACTOR 2-ALPHA KINASE; INITIATION-FACTOR; 4E; NF-KAPPA-B; ENDOPLASMIC-RETICULUM STRESS; STOMATITIS-VIRUS INFECTION; NEWLY SYNTHESIZED PROTEINS; MESSENGER-RNA;
D O I
10.1016/j.jmb.2018.04.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the early stages of infection, gaining control of the cellular protein synthesis machinery including its ribosomes is the ultimate combat objective for a virus. To successfully replicate, viruses unequivocally need to usurp and redeploy this machinery for translation of their own mRNA. In response, the host triggers global shutdown of translation while paradoxically allowing swift synthesis of antiviral proteins as a strategy to limit collateral damage. This fundamental conflict at the level of translational control defines the outcome of infection. As part of this special issue on molecular mechanisms of early virus host cell interactions, we review the current state of knowledge regarding translational control during viral infection with specific emphasis on protein kinase RNA-activated and mammalian target of rapamycin-mediated mechanisms. We also describe recent technological advances that will allow unprecedented insight into how viruses and host cells battle for ribosomes. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1965 / 1992
页数:28
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