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本文引用的文献

1
eIF5A promotes translation elongation, polysome disassembly and stress granule assembly.eIF5A 促进翻译延伸、多核糖体解体和应激颗粒组装。
PLoS One. 2010 Apr 1;5(4):e9942. doi: 10.1371/journal.pone.0009942.
2
USP10: friend and foe.USP10:朋友与敌人。
Cell. 2010 Feb 5;140(3):308-10. doi: 10.1016/j.cell.2010.01.034.
3
Histone acetyl transferases as emerging drug targets.组蛋白乙酰转移酶作为新兴的药物靶点。
Drug Discov Today. 2009 Oct;14(19-20):942-8. doi: 10.1016/j.drudis.2009.06.008. Epub 2009 Jul 2.
4
MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response.微小RNA介导的基因沉默调节紫外线诱导的DNA损伤反应。
EMBO J. 2009 Jul 22;28(14):2090-9. doi: 10.1038/emboj.2009.156. Epub 2009 Jun 18.
5
RNA granules: post-transcriptional and epigenetic modulators of gene expression.RNA颗粒:基因表达的转录后和表观遗传调节剂。
Nat Rev Mol Cell Biol. 2009 Jun;10(6):430-6. doi: 10.1038/nrm2694.
6
Hypusine-containing protein eIF5A promotes translation elongation.含hypusine的蛋白质eIF5A促进翻译延伸。
Nature. 2009 May 7;459(7243):118-21. doi: 10.1038/nature08034.
7
Polysomes, P bodies and stress granules: states and fates of eukaryotic mRNAs.多核糖体、P小体与应激颗粒:真核生物mRNA的状态与命运
Curr Opin Cell Biol. 2009 Jun;21(3):403-8. doi: 10.1016/j.ceb.2009.03.005. Epub 2009 Apr 23.
8
eIF5A has a function in the elongation step of translation in yeast.真核生物翻译起始因子5A(eIF5A)在酵母的翻译延伸步骤中发挥作用。
Biochem Biophys Res Commun. 2009 Mar 20;380(4):785-90. doi: 10.1016/j.bbrc.2009.01.148. Epub 2009 Jan 29.
9
Protein arginine methylation in mammals: who, what, and why.哺乳动物中的蛋白质精氨酸甲基化:何人、何物及为何。
Mol Cell. 2009 Jan 16;33(1):1-13. doi: 10.1016/j.molcel.2008.12.013.
10
The control of mRNA decapping and P-body formation.信使核糖核酸去帽作用及加工小体形成的调控
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翻译后修饰在应激颗粒组装中的作用。

The role of posttranslational modifications in the assembly of stress granules.

机构信息

National Research Lab for RNA Cell Biology, BK21 Graduate Program for RNA Biology and Department of Molecular Biology, Dankook University, Gyeonggi-do 448-701, South Korea.

出版信息

Wiley Interdiscip Rev RNA. 2010 Nov-Dec;1(3):486-93. doi: 10.1002/wrna.23.

DOI:10.1002/wrna.23
PMID:21956944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7169689/
Abstract

Stress granules (SGs) are aggregates of translationally silenced messenger ribonucleoprotein (mRNP) complexes induced by oxidative, osmotic, hypoxic, thermal, viral, and genotoxic stresses. Over the past decade, extensive research has identified key components of SGs, their molecular interactions, and impact on stress-induced reprogramming of protein expression and cell survival. However, studies defining the signaling pathways that modulate SG assembly have only been launched recently. These studies reveal that posttranslational modifications of selected SG proteins play important roles in the regulation of SG assembly and function. Here we provide an overview of the signaling pathways and posttranslational protein modifications that regulate the assembly and function of SGs.

摘要

应激颗粒(SGs)是由氧化、渗透、缺氧、热、病毒和基因毒性应激诱导产生的翻译沉默信使核糖核蛋白(mRNP)复合物聚集体。在过去十年中,广泛的研究已经确定了应激颗粒的关键成分、它们的分子相互作用,以及对应激诱导的蛋白质表达重编程和细胞存活的影响。然而,关于调控应激颗粒组装的信号通路的研究直到最近才开始。这些研究表明,特定应激颗粒蛋白的翻译后修饰在应激颗粒组装和功能的调节中发挥着重要作用。在这里,我们概述了调控应激颗粒组装和功能的信号通路以及蛋白质翻译后修饰。