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本文引用的文献

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The intramembrane protease SPPL2a promotes B cell development and controls endosomal traffic by cleavage of the invariant chain.膜内蛋白酶 SPPL2a 通过切割不变链促进 B 细胞发育并控制内体运输。
J Exp Med. 2013 Jan 14;210(1):41-58. doi: 10.1084/jem.20121069. Epub 2012 Dec 24.
2
Doxorubicin blocks proliferation of cancer cells through proteolytic activation of CREB3L1.阿霉素通过CREB3L1的蛋白水解激活来阻断癌细胞的增殖。
Elife. 2012 Dec 18;1:e00090. doi: 10.7554/eLife.00090.
3
Foamy virus envelope protein is a substrate for signal peptide peptidase-like 3 (SPPL3).泡沫病毒包膜蛋白是信号肽肽酶样 3(SPPL3)的底物。
J Biol Chem. 2012 Dec 21;287(52):43401-9. doi: 10.1074/jbc.M112.371369. Epub 2012 Nov 6.
4
Epigenetic silencing of antiviral genes renders clones of Huh-7 cells permissive for hepatitis C virus replication.抗病毒基因的表观遗传沉默使 Huh-7 细胞克隆对丙型肝炎病毒复制具有易感性。
J Virol. 2013 Jan;87(1):659-65. doi: 10.1128/JVI.01984-12. Epub 2012 Oct 31.
5
Structural analysis of hepatitis C virus core-E1 signal peptide and requirements for cleavage of the genotype 3a signal sequence by signal peptide peptidase.丙型肝炎病毒核心-E1 信号肽的结构分析和信号肽肽酶切割 3a 基因型信号序列的要求。
J Virol. 2012 Aug;86(15):7818-28. doi: 10.1128/JVI.00457-12. Epub 2012 May 16.
6
Hepatitis C virus: a new class of virus associated with particles derived from very low-density lipoproteins.丙型肝炎病毒:一种与极低密度脂蛋白衍生颗粒相关的新型病毒。
Arterioscler Thromb Vasc Biol. 2012 May;32(5):1099-103. doi: 10.1161/ATVBAHA.111.241448.
7
Human cytomegalovirus UL40 signal peptide regulates cell surface expression of the NK cell ligands HLA-E and gpUL18.人类巨细胞病毒 UL40 信号肽调节 NK 细胞配体 HLA-E 和 gpUL18 的细胞表面表达。
J Immunol. 2012 Mar 15;188(6):2794-804. doi: 10.4049/jimmunol.1102068. Epub 2012 Feb 15.
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Reducing HPV-associated cancer globally.全球减少 HPV 相关癌症。
Cancer Prev Res (Phila). 2012 Jan;5(1):18-23. doi: 10.1158/1940-6207.CAPR-11-0542.
9
Analysis of genes regulated by the transcription factor LUMAN identifies ApoA4 as a target gene in dendritic cells.分析转录因子 LUMAN 调控的基因,鉴定出 ApoA4 是树突状细胞中的一个靶基因。
Mol Immunol. 2012 Feb;50(1-2):66-73. doi: 10.1016/j.molimm.2011.12.003. Epub 2011 Dec 30.
10
The membrane-bound transcription factor CREB3L1 is activated in response to virus infection to inhibit proliferation of virus-infected cells.膜结合转录因子 CREB3L1 在病毒感染时被激活,以抑制被病毒感染的细胞的增殖。
Cell Host Microbe. 2011 Jul 21;10(1):65-74. doi: 10.1016/j.chom.2011.06.006.

膜内蛋白水解调控在病毒感染和抗病毒免疫中的作用。

Roles of regulated intramembrane proteolysis in virus infection and antiviral immunity.

作者信息

Ye Jin

机构信息

Department of Molecular Genetics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9046, USA.

出版信息

Biochim Biophys Acta. 2013 Dec;1828(12):2926-32. doi: 10.1016/j.bbamem.2013.05.005.

DOI:10.1016/j.bbamem.2013.05.005
PMID:24099010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3837687/
Abstract

Regulated intramembrane proteolysis (RIP) is a signaling mechanism through which transmembrane precursor proteins are cleaved to liberate their cytoplasmic and/or luminal/extracellular fragments from membranes so that these fragments are able to function at a new location. Recent studies have indicated that this proteolytic reaction plays an important role in host-virus interaction. On one hand, RIP transfers the signal from the endoplasmic reticulum (ER) to nucleus to activate antiviral genes in response to alteration of the ER caused by viral infection. On the other hand, RIP can be hijacked by virus to process transmembrane viral protein precursors and to destroy transmembrane antiviral proteins. Understanding this Yin and Yang side of RIP may lead to new strategies to combat viral infection. This article is part of a Special Issue entitled: Intramembrane Proteases.

摘要

调节性膜内蛋白水解(RIP)是一种信号传导机制,通过该机制,跨膜前体蛋白被切割,从而从膜上释放出其胞质和/或腔/细胞外片段,使这些片段能够在新的位置发挥作用。最近的研究表明,这种蛋白水解反应在宿主-病毒相互作用中起着重要作用。一方面,RIP将信号从内质网(ER)传递到细胞核,以响应病毒感染引起的内质网变化来激活抗病毒基因。另一方面,RIP可能被病毒劫持,用于处理跨膜病毒蛋白前体并破坏跨膜抗病毒蛋白。了解RIP的阴阳两面可能会带来对抗病毒感染的新策略。本文是名为:膜内蛋白酶的特刊的一部分。