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HIV-1感染需要功能性整合酶核定位信号。

HIV-1 infection requires a functional integrase NLS.

作者信息

Bouyac-Bertoia M, Dvorin J D, Fouchier R A, Jenkins Y, Meyer B E, Wu L I, Emerman M, Malim M H

机构信息

Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Mol Cell. 2001 May;7(5):1025-35. doi: 10.1016/s1097-2765(01)00240-4.

Abstract

HIV-1 is able to infect nondividing cells productively in part because the postentry viral nucleoprotein complexes are actively imported into the nucleus. In this manuscript, we identify a novel nuclear localization signal (NLS) in the viral integrase (IN) protein that is essential for virus replication in both dividing and nondividing cells. The IN NLS stimulates the efficient nuclear accumulation of viral DNA as well as virion-derived IN protein during the initial stages of infection but is dispensable for catalytic function. Because this NLS is required for infection irrespective of target cell proliferation, we suggest that interactions between uncoated viral nucleoprotein complexes and the host cell nuclear import machinery are critical for HIV-1 infection of all cells.

摘要

HIV-1能够有效感染非分裂细胞,部分原因是进入细胞后的病毒核蛋白复合物能被主动转运到细胞核中。在本论文中,我们在病毒整合酶(IN)蛋白中鉴定出一种新型核定位信号(NLS),它对于病毒在分裂细胞和非分裂细胞中的复制至关重要。在感染初期,IN NLS能刺激病毒DNA以及病毒体来源的IN蛋白高效地在细胞核中积累,但对于催化功能而言并非必需。由于无论靶细胞是否增殖,这种NLS都是感染所必需的,我们认为未包膜的病毒核蛋白复合物与宿主细胞核输入机制之间的相互作用对于HIV-1感染所有细胞至关重要。

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