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Differential restriction of human immunodeficiency virus type 2 and simian immunodeficiency virus SIVmac by TRIM5alpha alleles.TRIM5α等位基因对2型人类免疫缺陷病毒和猴免疫缺陷病毒SIVmac的差异性限制
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Gene therapy progress and prospects: development of improved lentiviral and retroviral vectors--design, biosafety, and production.基因治疗的进展与前景:改进型慢病毒和逆转录病毒载体的发展——设计、生物安全性及生产
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Molecular epidemiology of simian immunodeficiency virus SIVsm in U.S. primate centers unravels the origin of SIVmac and SIVstm.美国灵长类动物中心猿猴免疫缺陷病毒SIVsm的分子流行病学揭示了SIVmac和SIVstm的起源。
J Virol. 2005 Jul;79(14):8991-9005. doi: 10.1128/JVI.79.14.8991-9005.2005.
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J Virol. 2005 Jul;79(14):8969-78. doi: 10.1128/JVI.79.14.8969-8978.2005.
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A specific region of 37 amino acid residues in the SPRY (B30.2) domain of African green monkey TRIM5alpha determines species-specific restriction of simian immunodeficiency virus SIVmac infection.非洲绿猴TRIM5α的SPRY(B30.2)结构域中一段由37个氨基酸残基组成的特定区域决定了猿猴免疫缺陷病毒SIVmac感染的物种特异性限制。
J Virol. 2005 Jul;79(14):8870-7. doi: 10.1128/JVI.79.14.8870-8877.2005.
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TRIM5alpha selectively binds a restriction-sensitive retroviral capsid.TRIM5α 选择性结合一种对限制敏感的逆转录病毒衣壳。
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The contribution of RING and B-box 2 domains to retroviral restriction mediated by monkey TRIM5alpha.RING和B-box 2结构域对猴TRIM5α介导的逆转录病毒限制的贡献。
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ND10 components relocate to sites associated with herpes simplex virus type 1 nucleoprotein complexes during virus infection.在病毒感染期间,ND10成分会重新定位到与1型单纯疱疹病毒核蛋白复合物相关的位点。
J Virol. 2005 Apr;79(8):5078-89. doi: 10.1128/JVI.79.8.5078-5089.2005.
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Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection.急性猴免疫缺陷病毒(SIV)感染期间多个组织中出现大量感染及记忆性CD4 + T细胞丧失。
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三联基序蛋白对病毒感染性的控制

Control of viral infectivity by tripartite motif proteins.

作者信息

Towers Greg J

机构信息

Wohl Virion Centre, Infection and Immunity, University College London, London W1T 4JF, UK.

出版信息

Hum Gene Ther. 2005 Oct;16(10):1125-32. doi: 10.1089/hum.2005.16.1125.

DOI:10.1089/hum.2005.16.1125
PMID:16218773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3556579/
Abstract

It is of great interest to understand the molecular details of the pathways that constitute species barriers to viral infection. The tripartite motif protein TRIM5alpha has emerged as an important mediator of species-specific retroviral replication and innate immunity. This review considers the role of TRIM5alpha as an antiviral protein in mammals. The methods used to identify species-specific restriction to retroviral infection, and the identification of TRIM5alpha itself, are outlined. TRIM5alpha mediates an early postentry block to sensitive retroviral infection, usually before viral DNA synthesis. Results from mutational analysis of TRIM5alpha and their contribution to a mechanistic model for TRIM5alpha antiviral activity are discussed. The antiviral role of other TRIM proteins is considered, as is the role of TRIM5alpha cytoplasmic bodies.

摘要

了解构成病毒感染物种屏障的途径的分子细节具有重大意义。三联基序蛋白TRIM5α已成为物种特异性逆转录病毒复制和先天免疫的重要介质。本综述探讨了TRIM5α作为哺乳动物抗病毒蛋白的作用。概述了用于鉴定对逆转录病毒感染的物种特异性限制的方法以及TRIM5α本身的鉴定。TRIM5α介导对敏感逆转录病毒感染的早期进入后阻断,通常在病毒DNA合成之前。讨论了TRIM5α的突变分析结果及其对TRIM5α抗病毒活性机制模型的贡献。还考虑了其他TRIM蛋白的抗病毒作用以及TRIM5α细胞质小体的作用。