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编码芽殖酵母Cdc7相关激酶的人类和非洲爪蟾cDNA:一种假定的人类Cdc7同源物对MCM亚基的体外磷酸化作用

Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of MCM subunits by a putative human homologue of Cdc7.

作者信息

Sato N, Arai K, Masai H

机构信息

Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Minato-ku, Japan.

出版信息

EMBO J. 1997 Jul 16;16(14):4340-51. doi: 10.1093/emboj/16.14.4340.

Abstract

Saccharomyces cerevisiae Cdc7 kinase is essential for initiation of DNA replication, and Hsk1, a related kinase of Schizosaccharomyces pombe, is also required for DNA replication of fission yeast cells. We report here cDNAs encoding Cdc7-related kinases from human and Xenopus (huCdc7 and xeCdc7, respectively). The cloned cDNA for huCdc7 contains an open reading frame consisting of 574 amino acids with a predicted molecular weight of 63,847 that possesses overall amino acid identity of 32% (54% including similar residues) to Cdc7 and Hsk1. huCDC7 is transcribed in the various tissues examined, but most abundantly in testis. Three transcripts of 4.4, 3.5 and 2.4 kb in length are detected. The 3.5 kb transcript is the most predominant and is expressed in all the tissues examined. A cDNA containing a 91 nucleotide insertion at the N-terminal region of huCDC7 is also detected, suggesting the presence of multiple splicing variants. The huCdc7 protein is expressed at a constant level during the mitotic cell cycle and is localized primarily in nuclei in interphase and distributed diffusibly in cytoplasm in the mitotic phase. The wild-type huCdc7 protein expressed in COS7 cells phosphorylates MCM2 and MCM3 proteins in vitro, suggesting that huCdc7 may regulate processes of DNA replication by modulating MCM functions.

摘要

酿酒酵母Cdc7激酶对于DNA复制的起始至关重要,而粟酒裂殖酵母的相关激酶Hsk1对于裂殖酵母细胞的DNA复制也是必需的。我们在此报告了来自人类和非洲爪蟾(分别为huCdc7和xeCdc7)的编码Cdc7相关激酶的cDNA。克隆的huCdc7 cDNA包含一个由574个氨基酸组成的开放阅读框,预测分子量为63,847,与Cdc7和Hsk1的整体氨基酸同一性为32%(包括相似残基则为54%)。huCDC7在检测的各种组织中都有转录,但在睾丸中最为丰富。检测到长度为4.4、3.5和2.4 kb的三种转录本。3.5 kb的转录本最为主要,在所有检测的组织中都有表达。还检测到一个在huCDC7的N端区域含有91个核苷酸插入的cDNA,表明存在多种剪接变体。huCdc7蛋白在有丝分裂细胞周期中以恒定水平表达,在间期主要定位于细胞核,在有丝分裂期则在细胞质中弥散分布。在COS7细胞中表达的野生型huCdc7蛋白在体外可磷酸化MCM2和MCM3蛋白,这表明huCdc7可能通过调节MCM功能来调控DNA复制过程。

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