Direct activation of protein phosphatase-2A(0) by HIV-1 encoded protein complex NCp7:vpr

被引:43
作者
Tung, HYL
DeRocquigny, H
Zhao, LJ
Cayla, X
Rogues, BP
Ozon, R
机构
[1] CFSR BIOMED SCI INST,PROT & PEPTIDE RES LAB,HOUSTON,TX 77068
[2] CNRS,INSERM,U266,DEPT PHARMACOCHIM MOL & STRUCT,URA D 1500,F-75006 PARIS,FRANCE
[3] ST LOUIS UNIV,CTR HLTH SCI,SCH MED,INST MOL VIROL,ST LOUIS,MO 63110
关键词
Protein phosphatase-2A; HIV-1; NCp7; vpr;
D O I
10.1016/S0014-5793(96)01470-6
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
The effects of HIV-1 encoded proteins NCp7, vpr and NCp7:vpr complex on the activity of protein phosphatase-2A(0) have been tested, We report that NCp7 is an activator of protein phosphatase-2A(0) and that vpr activated protein phosphatase-2A(0) only slightly, We also report that NCp7 and vpr form a tight complex which becomes a more potent activator of protein phosphatase-2A(0) than NCp7 alone, The ability of NCp7 to activate protein phosphatase-2A(0) is regulated by vpr. The C-terminal portion of vpr prevents NCp7 from activating protein phosphatase-2A(0) while the N-terminal portion of vpr potentiates the effect of NCp7 on the activity of protein phosphatase-2A(0), Our findings indicate that vpr may be acting as a targeting subunit which directs NCp7 to activate protein phosphatase-2A(0), In view of the fact that protein phosphatase-2A functions as an inhibitor of G(0) to M transition of the cell cycle and is involved in other key cellular processes such as the control of RNA transcription, the results presented in this report may explain how HIV-1 causes cell cycle arrest which may lead to CD4+ T cell depletion and also how it disturbs normal cellular processes of its host cell.
引用
收藏
页码:197 / 201
页数:5
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