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减数第二次分裂起始和进行所需的新型裂殖酵母Cdc7-Dbf4样激酶复合物。

Novel fission yeast Cdc7-Dbf4-like kinase complex required for the initiation and progression of meiotic second division.

作者信息

Nakamura Taro, Nakamura-Kubo Michiko, Nakamura Tomohiro, Shimoda Chikashi

机构信息

Department of Biology, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka, Japan.

出版信息

Mol Cell Biol. 2002 Jan;22(1):309-20. doi: 10.1128/MCB.22.1.309-320.2002.

Abstract

Cdc7, a conserved serine/threonine protein kinase, controls initiation of DNA replication. A regulatory subunit, Dbf4, stimulates the kinase activity of Cdc7 and recruits it to the replication origins. Schizosaccharomyces pombe has a homologous kinase complex, composed of Hsk1 and Dfp1/Him1. Here, we report a novel protein kinase of S. pombe, Spo4, which shares common structural features with the Cdc7 kinases. In spite of the structural similarities, Spo4 is dispensable for mitotic growth and premeiotic DNA replication. Intriguingly, spo4 null mutants are defective in initiation and progression of the second meiotic division. Spindles for meiosis II are often fragmented. Spo4 kinase activity is markedly enhanced when the enzyme is associated with its regulatory subunit, Spo6, a Dbf4-like protein. Expression of Spo4 is specifically induced during meiosis. Spo4 is preferentially present in nuclei, but this nuclear localization does not require Spo6. These results suggest that Spo4 is a Cdc7 kinase whose primary role is in meiosis, not in DNA replication. This is the first report of an organism which has two Cdc7-related kinase complexes with different biological functions.

摘要

Cdc7是一种保守的丝氨酸/苏氨酸蛋白激酶,可控制DNA复制的起始。一个调节亚基Dbf4可刺激Cdc7的激酶活性,并将其招募到复制起点。粟酒裂殖酵母具有一种同源激酶复合物,由Hsk1和Dfp1/Him1组成。在此,我们报道了粟酒裂殖酵母的一种新型蛋白激酶Spo4,它与Cdc7激酶具有共同的结构特征。尽管结构相似,但Spo4对于有丝分裂生长和减数分裂前的DNA复制并非必需。有趣的是,spo4缺失突变体在第二次减数分裂的起始和进行过程中存在缺陷。减数分裂II的纺锤体经常碎片化。当Spo4激酶与其调节亚基Spo6(一种类似Dbf4的蛋白)结合时,其激酶活性会显著增强。Spo4的表达在减数分裂过程中被特异性诱导。Spo4优先存在于细胞核中,但这种核定位并不需要Spo6。这些结果表明,Spo4是一种Cdc7激酶,其主要作用是在减数分裂中,而非DNA复制中。这是关于一种生物体具有两种具有不同生物学功能的Cdc7相关激酶复合物的首次报道。

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