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首页> 外文期刊>The Korean Journal of Genetics >Phosphorylation of Mcm2 protein by Cdc7 kinase is not essential for the initiation of DNA replication in fission yeast
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Phosphorylation of Mcm2 protein by Cdc7 kinase is not essential for the initiation of DNA replication in fission yeast

机译:Cdc7激酶使Mcm2蛋白磷酸化对于裂变酵母中DNA复制的启动不是必需的

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摘要

Previous studies in many species suggested that the minichromosome maintenance complex is a major physiological target of Cdc7. In this study, we examined the cellular role of Mcm2 phosphorylation by Cdc7 kinase in Schizosaccharomyces pombe. The in vitro phosphorylation of several truncated Mcm2 proteins by Cdc7 kinase showed that the major phosphorylation sites were located at N-terminus of Mcm2 protein. Alanine substitutions of several putative Cdc7 phosphorylation sites in this region resulted in the mutant Mcm2 proteins which were hardly phosphorylated by Cdc7 kinase in vitro. When these proteins were expressed in mcm2 mutant cells, all of alanine substituted mutant proteins still complemented the temperature sensitive phenotype of mutant cells. These results suggest that the phosphorylation of Mcm2 protein by Cdc7 kinase is not essential for the initiation of DNA replication. Cdc7 may play its essential roles by phosphorylating other Mcm subunits or proteins involved in the initiation of DNA replication.
机译:先前在许多物种中的研究表明,微染色体维持复合物是Cdc7的主要生理目标。在这项研究中,我们检查了粟酒裂殖酵母中Cdc7激酶对Mcm2磷酸化的细胞作用。 Cdc7激酶对几种截短的Mcm2蛋白的体外磷酸化显示,主要的磷酸化位点位于Mcm2蛋白的N末端。在该区域中几个假定的Cdc7磷酸化位点的丙氨酸取代导致突变的Mcm2蛋白在体外几乎不被Cdc7激酶磷酸化。当这些蛋白质在mcm2突变细胞中表达时,所有丙氨酸取代的突变蛋白仍与突变细胞的温度敏感表型互补。这些结果表明,Cdc7激酶使Mcm2蛋白磷酸化对于DNA复制的启动不是必需的。 Cdc7可能通过使参与DNA复制起始的其他Mcm亚基或蛋白质磷酸化而发挥其重要作用。

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