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2
Transient and stable knockdown of the integrase cofactor LEDGF/p75 reveals its role in the replication cycle of human immunodeficiency virus.整合酶辅因子LEDGF/p75的瞬时和稳定敲低揭示了其在人类免疫缺陷病毒复制周期中的作用。
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Self-limiting, cell type-dependent replication of an integrase-defective human immunodeficiency virus type 1 in human primary macrophages but not T lymphocytes.整合酶缺陷型1型人类免疫缺陷病毒在人原代巨噬细胞中而非T淋巴细胞中进行自我限制、细胞类型依赖性复制。
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Expression analysis of LEDGF/p75, APOBEC3G, TRIM5alpha, and tetherin in a Senegalese cohort of HIV-1-exposed seronegative individuals.在塞内加尔的一组 HIV-1 暴露但血清阴性的个体中,对 LEDGF/p75、APOBEC3G、TRIM5alpha 和 tetherin 的表达进行分析。
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本文引用的文献

1
Importin 7 may be dispensable for human immunodeficiency virus type 1 and simian immunodeficiency virus infection of primary macrophages.输入蛋白7对于原代巨噬细胞的1型人类免疫缺陷病毒和猿猴免疫缺陷病毒感染可能并非必需。
J Virol. 2005 Sep;79(17):11541-6. doi: 10.1128/JVI.79.17.11541-11546.2005.
2
Solution structure of the HIV-1 integrase-binding domain in LEDGF/p75.LEDGF/p75中HIV-1整合酶结合结构域的溶液结构
Nat Struct Mol Biol. 2005 Jun;12(6):526-32. doi: 10.1038/nsmb937. Epub 2005 May 15.
3
Integrase mutants defective for interaction with LEDGF/p75 are impaired in chromosome tethering and HIV-1 replication.与LEDGF/p75相互作用存在缺陷的整合酶突变体在染色体锚定和HIV-1复制方面受损。
J Biol Chem. 2005 Jul 8;280(27):25517-23. doi: 10.1074/jbc.M501378200. Epub 2005 Apr 25.
4
Identification of the LEDGF/p75 HIV-1 integrase-interaction domain and NLS reveals NLS-independent chromatin tethering.LEDGF/p75 HIV-1整合酶相互作用结构域和核定位信号的鉴定揭示了不依赖核定位信号的染色质锚定。
J Cell Sci. 2005 Apr 15;118(Pt 8):1733-43. doi: 10.1242/jcs.02299. Epub 2005 Mar 29.
5
The interaction of LEDGF/p75 with integrase is lentivirus-specific and promotes DNA binding.LEDGF/p75与整合酶的相互作用具有慢病毒特异性,并促进DNA结合。
J Biol Chem. 2005 May 6;280(18):17841-7. doi: 10.1074/jbc.M411681200. Epub 2005 Mar 4.
6
Class II integrase mutants with changes in putative nuclear localization signals are primarily blocked at a postnuclear entry step of human immunodeficiency virus type 1 replication.在假定的核定位信号上发生改变的II类整合酶突变体主要在1型人类免疫缺陷病毒复制的核进入后步骤被阻断。
J Virol. 2004 Dec;78(23):12735-46. doi: 10.1128/JVI.78.23.12735-12746.2004.
7
Identification of an evolutionarily conserved domain in human lens epithelium-derived growth factor/transcriptional co-activator p75 (LEDGF/p75) that binds HIV-1 integrase.在人晶状体上皮衍生生长因子/转录共激活因子p75(LEDGF/p75)中鉴定出与HIV-1整合酶结合的进化保守结构域。
J Biol Chem. 2004 Nov 19;279(47):48883-92. doi: 10.1074/jbc.M406307200. Epub 2004 Sep 14.
8
LEDGF/p75 determines cellular trafficking of diverse lentiviral but not murine oncoretroviral integrase proteins and is a component of functional lentiviral preintegration complexes.LEDGF/p75决定多种慢病毒而非鼠类致癌逆转录病毒整合酶蛋白的细胞转运,并且是功能性慢病毒整合前复合物的一个组成部分。
J Virol. 2004 Sep;78(17):9524-37. doi: 10.1128/JVI.78.17.9524-9537.2004.
9
LEDGF/p75 is essential for nuclear and chromosomal targeting of HIV-1 integrase in human cells.LEDGF/p75对于HIV-1整合酶在人类细胞中的细胞核及染色体靶向定位至关重要。
J Biol Chem. 2003 Aug 29;278(35):33528-39. doi: 10.1074/jbc.M303594200. Epub 2003 Jun 9.
10
The barrier-to-autointegration factor is a component of functional human immunodeficiency virus type 1 preintegration complexes.自整合屏障因子是功能性1型人类免疫缺陷病毒整合前复合物的一个组成部分。
J Virol. 2003 Apr;77(8):5030-6. doi: 10.1128/jvi.77.8.5030-5036.2003.

LEDGFp75基因沉默后,巨噬细胞中人类免疫缺陷病毒1型感染受到适度但可重复的抑制。

Modest but reproducible inhibition of human immunodeficiency virus type 1 infection in macrophages following LEDGFp75 silencing.

作者信息

Zielske Steven P, Stevenson Mario

机构信息

Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, 01605, USA.

出版信息

J Virol. 2006 Jul;80(14):7275-80. doi: 10.1128/JVI.02470-05.

DOI:10.1128/JVI.02470-05
PMID:16809334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1489053/
Abstract

LEDGFp75 is a cellular protein which binds human immunodeficiency virus type 1 (HIV-1) integrase with high specificity and affinity but whose function in infection has not been defined. We infected LEDGFp75-deficient primary macrophages with wild-type HIV in order to assess potential infection phenotypes which would provide clues to LEDGFp75 function. Silencing of LEDGFp75 by 70 to 80% resulted in an average of 53% reduced infection of macrophages by HIV. Analysis of infection intermediates showed that integration, but not two-long-terminal-repeat (2LTR) circles or late cDNAs, was reduced up to 74% in LEDGFp75-deficient macrophages. Therefore, LEDGFp75 has a modest involvement in HIV-1 integration in macrophages.

摘要

LEDGFp75是一种细胞蛋白,它能以高特异性和亲和力与人免疫缺陷病毒1型(HIV-1)整合酶结合,但其在感染过程中的功能尚未明确。我们用野生型HIV感染LEDGFp75缺陷的原代巨噬细胞,以评估可能的感染表型,这些表型可为LEDGFp75的功能提供线索。LEDGFp75沉默70%至80%导致HIV对巨噬细胞的感染平均减少53%。对感染中间体的分析表明,在LEDGFp75缺陷的巨噬细胞中,整合过程(而非双长末端重复序列(2LTR)环或晚期cDNA)减少了74%。因此,LEDGFp75在巨噬细胞的HIV-1整合过程中起适度作用。