Ultrasensitivity in the Regulation of Cdc25C by Cdk1

被引:110
|
作者
Trunnell, Nicole B. [1 ,2 ]
Poon, Andy C. [1 ]
Kim, Sun Young [1 ]
Ferrell, James E., Jr. [1 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Program Canc Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
CELL-CYCLE REGULATION; DNA-DAMAGE CHECKPOINT; XENOPUS EGG EXTRACTS; M-PHASE; MULTISITE PHOSPHORYLATION; MITOTIC INDUCER; PROTEIN-KINASE; G(2)/M TRANSITION; INHIBITORY KINASE; FISSION YEAST;
D O I
10.1016/j.molcel.2011.01.012
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
Cdc25C is a critical component of the interlinked positive and double-negative feedback loops that constitute the bistable mitotic trigger. Computational studies have indicated that the trigger's bistability should be more robust if the individual legs of the loops exhibit ultrasensitive responses. Here, we show that in Xenopus extracts two measures of Cdc25C activation (hyperphosphorylation and Ser 287 dephosphorylation) are highly ultrasensitive functions of the Cdk1 activity; estimated Hill coefficients were 11 to 32. Some of Cdc25C's ultrasensitivity can be reconstituted in vitro with purified components, and the reconstituted ultrasensitivity depends upon multisite phosphorylation. The response functions determined here for Cdc25C and previously for Wee1A allow us to formulate a simple mathematical model of the transition between interphase and mitosis. The model shows how the continuously variable regulators of mitosis work collectively to generate a switch-like, hysteretic response.
引用
收藏
页码:263 / 274
页数:12
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