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HIV-1基质蛋白中的两个核定位信号调节HIV-1整合前复合物的核输入。

Two nuclear localization signals in the HIV-1 matrix protein regulate nuclear import of the HIV-1 pre-integration complex.

作者信息

Haffar O K, Popov S, Dubrovsky L, Agostini I, Tang H, Pushkarsky T, Nadler S G, Bukrinsky M

机构信息

Cytokine Networks Inc., Seattle, WA, 98119, USA.

出版信息

J Mol Biol. 2000 Jun 2;299(2):359-68. doi: 10.1006/jmbi.2000.3768.

Abstract

Replication of HIV-1 in non-dividing and slowly proliferating cell populations depends on active import of the viral pre-integration complex (PIC) into the cell nucleus. While it is commonly accepted that this process is mediated by an interaction between the HIV-1 PIC and the cellular nuclear import machinery, controversial results have been reported concerning the mechanisms of this interaction. Here, we demonstrate that a recently identified nuclear localization signal within the HIV-1 matrix protein (MA), MA NLS-2, together with previously described MA NLS-1, mediates nuclear import of the HIV-1 PIC. Inactivation of both MA NLSs precluded nuclear translocation of MA and rendered the virus defective in nuclear import and replication in non-dividing macrophage cultures, even when functional Vpr and integrase (IN), two more viral proteins implicated in HIV-1 nuclear import, were present. Taken together, these results indicate that Vpr does not function as an independent nuclear import factor and demonstrate that HIV-1 MA, by virtue of its two nuclear localization signals, regulates HIV-1 nuclear import.

摘要

HIV-1在非分裂和缓慢增殖的细胞群体中的复制依赖于病毒前整合复合物(PIC)主动导入细胞核。虽然人们普遍认为这一过程是由HIV-1 PIC与细胞的核输入机制之间的相互作用介导的,但关于这种相互作用的机制已有一些有争议的报道。在此,我们证明,HIV-1基质蛋白(MA)中最近鉴定出的一个核定位信号MA NLS-2,与先前描述的MA NLS-1一起,介导HIV-1 PIC的核输入。两个MA NLS均失活会阻止MA的核转位,并使病毒在非分裂巨噬细胞培养物中的核输入和复制出现缺陷,即使存在另外两种与HIV-1核输入有关的病毒蛋白功能性Vpr和整合酶(IN)。综上所述,这些结果表明Vpr并非作为一个独立的核输入因子发挥作用,并证明HIV-1 MA凭借其两个核定位信号调节HIV-1的核输入。

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