HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VPR ARRESTS THE CELL-CYCLE IN G(2) BY INHIBITING THE ACTIVATION OF P34(CDC2)-CYCLIN-B

被引:334
|
作者
RE, F
BRAATEN, D
FRANKE, EK
LUBAN, J
机构
[1] COLUMBIA UNIV,COLL PHYS & SURG,DEPT MICROBIOL,NEW YORK,NY 10032
[2] COLUMBIA UNIV,COLL PHYS & SURG,DEPT MED,NEW YORK,NY 10032
关键词
D O I
10.1128/JVI.69.11.6859-6864.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human immunodeficiency virus type 1 (HIV-1) vpr inhibits the replication of tumor cell lines and peripheral blood mononuclear cells. Here it is demonstrated that expression of vpr, either in the context of a provirus or from an independent genetic element, induces a discrete cell cycle arrest, with cells containing 4N DNA. Low cyclin B-associated kinase activity, as well as the status of p34(cdc2) and cdc25C phosphorylation, indicates that the cascade of reactions which drives the cell into mitosis has not been initiated, The phosphatase inhibitor okadaic acid releases the block, suggesting that Vpr perturbs upstream regulators of the G(2)-M transition. These studies demonstrate that HIV-1 vpr has profound effects on the cellular factors which control entry into mitosis and indicate vpr's potential contribution to the cellular pathology associated with HIV-1 infection.
引用
收藏
页码:6859 / 6864
页数:6
相关论文
共 50 条