HIV-1 infection requires a functional integrase NLS

被引:171
作者
Bouyac-Bertoia, M
Dvorin, JD
Fouchier, RAM
Jenkins, Y
Meyer, BE
Wu, LI
Emerman, M
Malim, MH [1 ]
机构
[1] Univ Penn, Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
[4] Erasmus Univ, Dept Virol, NL-3000 DR Rotterdam, Netherlands
[5] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
关键词
D O I
10.1016/S1097-2765(01)00240-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1025 / 1035
页数:11
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