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本文引用的文献

1
Stress Granules and Processing Bodies in Translational Control.应激颗粒和翻译调控中的加工体
Cold Spring Harb Perspect Biol. 2019 May 1;11(5):a032813. doi: 10.1101/cshperspect.a032813.
2
Ribosome Profiling: Global Views of Translation.核糖体图谱分析:翻译的全局观。
Cold Spring Harb Perspect Biol. 2019 May 1;11(5):a032698. doi: 10.1101/cshperspect.a032698.
3
The Epitranscriptome in Translation Regulation.翻译调控中的表观转录组
Cold Spring Harb Perspect Biol. 2019 Aug 1;11(8):a032623. doi: 10.1101/cshperspect.a032623.
4
Phosphorylation and Signal Transduction Pathways in Translational Control.翻译:翻译为简体中文输出
Cold Spring Harb Perspect Biol. 2019 Jul 1;11(7):a033050. doi: 10.1101/cshperspect.a033050.
5
Noncanonical Translation Initiation in Eukaryotes.真核生物中的非规范翻译起始。
Cold Spring Harb Perspect Biol. 2019 Apr 1;11(4):a032672. doi: 10.1101/cshperspect.a032672.
6
Defining the Role of Stress Granules in Innate Immune Suppression by the Herpes Simplex Virus 1 Endoribonuclease VHS.定义单纯疱疹病毒 1 内切核糖核酸酶 VHS 在先天免疫抑制中的应激颗粒作用。
J Virol. 2018 Jul 17;92(15). doi: 10.1128/JVI.00829-18. Print 2018 Aug 1.
7
Protein Synthesis Initiation in Eukaryotic Cells.真核细胞中的蛋白质合成起始。
Cold Spring Harb Perspect Biol. 2018 Dec 3;10(12):a033092. doi: 10.1101/cshperspect.a033092.
8
Translation Elongation and Recoding in Eukaryotes.真核生物中的翻译延伸和重编码。
Cold Spring Harb Perspect Biol. 2018 Aug 1;10(8):a032649. doi: 10.1101/cshperspect.a032649.
9
The Initiation Factors eIF2, eIF2A, eIF2D, eIF4A, and eIF4G Are Not Involved in Translation Driven by Hepatitis C Virus IRES in Human Cells.起始因子eIF2、eIF2A、eIF2D、eIF4A和eIF4G不参与丙型肝炎病毒内部核糖体进入位点在人细胞中驱动的翻译过程。
Front Microbiol. 2018 Feb 13;9:207. doi: 10.3389/fmicb.2018.00207. eCollection 2018.
10
Role of eIF2α Kinases in Translational Control and Adaptation to Cellular Stress.真核起始因子 2α 激酶在翻译调控和细胞应激适应中的作用。
Cold Spring Harb Perspect Biol. 2018 Jul 2;10(7):a032870. doi: 10.1101/cshperspect.a032870.

病毒感染细胞中的翻译调控。

Translational Control in Virus-Infected Cells.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294.

出版信息

Cold Spring Harb Perspect Biol. 2019 Mar 1;11(3):a033001. doi: 10.1101/cshperspect.a033001.

DOI:10.1101/cshperspect.a033001
PMID:29891561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6396331/
Abstract

As obligate intracellular parasites, virus reproduction requires host cell functions. Despite variations in genome size and configuration, nucleic acid composition, and their repertoire of encoded functions, all viruses remain unconditionally dependent on the protein synthesis machinery resident within their cellular hosts to translate viral messenger RNAs (mRNAs). A complex signaling network responsive to physiological stress, including infection, regulates host translation factors and ribosome availability. Furthermore, access to the translation apparatus is patrolled by powerful host immune defenses programmed to restrict viral invaders. Here, we review the tactics and mechanisms used by viruses to appropriate control over host ribosomes, subvert host defenses, and dominate the infected cell translational landscape. These not only define aspects of infection biology paramount for virus reproduction, but continue to drive fundamental discoveries into how cellular protein synthesis is controlled in health and disease.

摘要

作为专性细胞内寄生虫,病毒的繁殖需要宿主细胞的功能。尽管基因组大小和结构、核酸组成以及编码功能的种类存在差异,但所有病毒仍然无条件地依赖于其宿主细胞中存在的蛋白质合成机制来翻译病毒信使 RNA(mRNA)。一个对生理应激(包括感染)有反应的复杂信号网络调节宿主翻译因子和核糖体的可用性。此外,对翻译装置的访问受到强大的宿主免疫防御机制的控制,这些防御机制旨在限制病毒入侵。在这里,我们回顾了病毒用来控制宿主核糖体、颠覆宿主防御并主导受感染细胞翻译景观的策略和机制。这些不仅定义了感染生物学中对病毒繁殖至关重要的方面,而且还不断推动对细胞蛋白质合成在健康和疾病中如何受到控制的基本发现。