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Wee1 检查点抑制后期起始。

A Wee1 checkpoint inhibits anaphase onset.

机构信息

Ottawa Institute of Systems Biology and Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario K1H 8M5, Canada.

出版信息

J Cell Biol. 2013 Jun 10;201(6):843-62. doi: 10.1083/jcb.201212038.

Abstract

Cdk1 drives both mitotic entry and the metaphase-to-anaphase transition. Past work has shown that Wee1 inhibition of Cdk1 blocks mitotic entry. Here we show that the budding yeast Wee1 kinase, Swe1, also restrains the metaphase-to-anaphase transition by preventing Cdk1 phosphorylation and activation of the mitotic form of the anaphase-promoting complex/cyclosome (APC(Cdc20)). Deletion of SWE1 or its opposing phosphatase MIH1 (the budding yeast cdc25(+)) altered the timing of anaphase onset, and activation of the Swe1-dependent morphogenesis checkpoint or overexpression of Swe1 blocked cells in metaphase with reduced APC activity in vivo and in vitro. The morphogenesis checkpoint also depended on Cdc55, a regulatory subunit of protein phosphatase 2A (PP2A). cdc55Δ checkpoint defects were rescued by mutating 12 Cdk1 phosphorylation sites on the APC, demonstrating that the APC is a target of this checkpoint. These data suggest a model in which stepwise activation of Cdk1 and inhibition of PP2A(Cdc55) triggers anaphase onset.

摘要

Cdk1 驱动有丝分裂的进入和中期到后期的转变。过去的工作表明,Wee1 对 Cdk1 的抑制阻止了有丝分裂的进入。在这里,我们表明, budding yeast Wee1 激酶 Swe1 也通过阻止 Cdk1 的磷酸化和激活有丝分裂形式的后期促进复合物/环体(APC(Cdc20))来限制中期到后期的转变。SWE1 的缺失或其相反的磷酸酶 MIH1( budding yeast cdc25(+))改变了后期开始的时间,激活 Swe1 依赖性形态发生检查点或过表达 Swe1 会导致细胞在体内和体外处于中期,APC 活性降低。形态发生检查点也依赖于 Cdc55,它是蛋白磷酸酶 2A(PP2A)的调节亚基。cdc55Δ 检查点缺陷可以通过突变 APC 上的 12 个 Cdk1 磷酸化位点来挽救,这表明 APC 是这个检查点的一个靶点。这些数据表明,Cdk1 的逐步激活和 PP2A(Cdc55)的抑制触发了后期的开始。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d822/3678162/2f9abc78e292/JCB_201212038R_Fig1.jpg

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