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通过化学遗传学方法在脊椎动物细胞中揭示了Cdk1在S期调控中的重要作用。

An essential role for Cdk1 in S phase control is revealed via chemical genetics in vertebrate cells.

作者信息

Hochegger Helfrid, Dejsuphong Donniphat, Sonoda Eiichiro, Saberi Alihossein, Rajendra Eeson, Kirk Jane, Hunt Tim, Takeda Shunichi

机构信息

Department of Radiation Genetics, Kyoto University Graduate School of Medicine, Kyoto, Japan.

出版信息

J Cell Biol. 2007 Jul 16;178(2):257-68. doi: 10.1083/jcb.200702034.

Abstract

In vertebrates Cdk1 is required to initiate mitosis; however, any functionality of this kinase during S phase remains unclear. To investigate this, we generated chicken DT40 mutants, in which an analog-sensitive mutant cdk1 as replaces the endogenous Cdk1, allowing us to specifically inactivate Cdk1 using bulky ATP analogs. In cells that also lack Cdk2, we find that Cdk1 activity is essential for DNA replication initiation and centrosome duplication. The presence of a single Cdk2 allele renders S phase progression independent of Cdk1, which suggests a complete overlap of these kinases in S phase control. Moreover, we find that Cdk1 inhibition did not induce re-licensing of replication origins in G2 phase. Conversely, inhibition during mitosis of Cdk1 causes rapid activation of endoreplication, depending on proteolysis of the licensing inhibitor Geminin. This study demonstrates essential functions of Cdk1 in the control of S phase, and exemplifies a chemical genetics approach to target cyclin-dependent kinases in vertebrate cells.

摘要

在脊椎动物中,Cdk1是启动有丝分裂所必需的;然而,该激酶在S期的任何功能仍不清楚。为了对此进行研究,我们构建了鸡DT40突变体,其中一个对类似物敏感的突变型cdk1替代了内源性Cdk1,这使我们能够使用庞大的ATP类似物特异性地使Cdk1失活。在同时也缺乏Cdk2的细胞中,我们发现Cdk1活性对于DNA复制起始和中心体复制至关重要。单个Cdk2等位基因的存在使S期进程独立于Cdk1,这表明这些激酶在S期控制中完全重叠。此外,我们发现抑制Cdk1不会在G2期诱导复制起点的重新许可。相反,在有丝分裂期间抑制Cdk1会导致内复制的快速激活,这取决于许可抑制剂Geminin的蛋白水解。这项研究证明了Cdk1在S期控制中的重要功能,并举例说明了一种在脊椎动物细胞中靶向细胞周期蛋白依赖性激酶的化学遗传学方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0513/2064445/5dc3a1138de5/jcb1780257f01.jpg

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