Phosphorylation of Vpr regulates HIV type 1 nuclear import and macrophage infection

被引:34
作者
Agostini, I
Popov, S
Hao, T
Li, JH
Dubrovsky, L
Chaika, O
Chaika, N
Lewis, R
Bukrinsky, M
机构
[1] George Washington Univ, Dept Microbiol & Trop Med, Washington, DC 20037 USA
[2] Picower Inst Med Res, Manhasset, NY 11030 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Zycos, Cambridge, MA 02138 USA
[5] Eppley Canc Inst, Omaha, NE 68198 USA
关键词
D O I
10.1089/088922202753472856
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Viral protein R (Vpr) of human immunodeficiency virus type 1 (HIV-1) is a small accessory protein that regulates nuclear import of the viral preintegration complex and facilitates infection of nondividing cells, such as macrophages. Studies demonstrated that a fraction of Vpr molecules is phosphorylated in the virions and in HIV-1-infected cells, but the role of phosphorylation in nuclear import activity of Vpr has not been established. We found that Vpr is phosphorylated predominantly on the serine residue in position 79, and mutations affecting Vpr phosphorylation significantly attenuated viral replication in macrophages, but not in activated T lymphocytes or cell lines. The replication defect was mapped by polymerase chain reaction analysis to the step of nuclear import. These results suggest that phosphorylation of Vpr regulates its activity in the nuclear import of the HIV-1 preintegration complex.
引用
收藏
页码:283 / 288
页数:6
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