The Dcr2p phosphatase destabilizes Sic1p in Saccharomyces cerevisiae

被引:7
|
作者
Pathak, Ritu [1 ]
Blank, Heidi Nl [1 ]
Guo, Jinbal [1 ]
Ellis, Sarah [1 ]
Polymenis, Michael [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
关键词
DCR2; SICl; START; cell cycle;
D O I
10.1016/j.bbrc.2007.07.092
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
Initiation of cell division is controlled by an irreversible switch. In Saccharomyces cerevisiae degradation of the Sic1p protein, an inhibitor of mitotic cyclin/cyclin-dependent kinase complexes, takes place before initiation of DNA replication, at a point called START. Sic1p is phosphorylated by multiple kinases, which can differentially affect the stability of Sic1p. How phosphorylations that stabilize Sic1p, are reversed is unknown. Here we show that the Dcr2p phosphatase functionally and physically interacts with Sic1p. Over-expression of Dcr2p destabilizes Sic I p and leads to phenotypes associated with destabilized Sic1p, such as genome instability. Our results identify a novel factor that affects the stability of Sic1p, possibly contributing to mechanisms that trigger initiation of cell division. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:700 / 704
页数:5
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