Reovirus-induced σ1s-dependent G2/M phase cell cycle arrest is associated with inhibition of p34cdc2

被引:48
作者
Poggioli, GJ
Dermody, TS
Tyler, KL
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Neurol B 182, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Microbiol, Denver, CO 80262 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80262 USA
[5] Denver Vet Affairs Med Ctr, Neurol Serv, Denver, CO 80220 USA
[6] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37232 USA
[7] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37232 USA
[8] Vanderbilt Univ, Sch Med, Elizabeth B Lamb Ctr Pediat Res, Nashville, TN 37232 USA
关键词
D O I
10.1128/JVI.75.16.7429-7434.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Serotype 3 reoviruses inhibit cellular proliferation by inducing a G(2)/M phase cell cycle arrest. Reovirus-induced G(2)/M phase arrest requires the viral S1 gene-encoded sigma 1s nonstructural protein. The G(2)-to-M transition represents a cell cycle checkpoint that is regulated by the kinase p34(cd2). We now report that infection with serotype 3 reovirus strain Abney, but not serotype I reovirus strain Lang, is associated with inhibition and hyperphosphorylation of p34(cdc2). The als protein is necessary and sufficient for inhibitory phosphorylation of p34(cdc2), since a viral mutant lacking als fails to hyperphosphorylate p34(cdc2) and inducible expression of als is sufficient for p34(cdc2) hyperphosphorylation. These studies establish a mechanism by which reovirus can perturb cell cycle regulation.
引用
收藏
页码:7429 / 7434
页数:6
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