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DNA复制的细胞周期调控

Cell cycle control of DNA replication.

作者信息

Stillman B

机构信息

Cold Spring Harbor Laboratory, P.O. Box 100, Cold Spring Harbor, NY 11724, USA.

出版信息

Science. 1996 Dec 6;274(5293):1659-64. doi: 10.1126/science.274.5293.1659.

DOI:10.1126/science.274.5293.1659
PMID:8939847
Abstract

The initiation of DNA replication in eukaryotic cells is a highly regulated process that leads to the duplication of the genetic information for the next cell generation. This requires the ordered assembly of many proteins at the origins of DNA replication to form a competent, pre-replicative chromosomal state. In addition to this competent complex, at least two cell cycle regulated protein kinase pathways are required to affect a transition to a post-replicative chromosomal state. Protein kinases required to establish mitosis prevent re-replication of the DNA. As cells exit mitosis, the cell cycle is reset, allowing the establishment of a new, competent replication state.

摘要

真核细胞中DNA复制的起始是一个高度调控的过程,它导致遗传信息复制以传递给下一代细胞。这需要许多蛋白质在DNA复制起点有序组装,以形成一个有活性的、复制前的染色体状态。除了这个有活性的复合物外,至少还需要两条受细胞周期调控的蛋白激酶途径来促使向复制后染色体状态转变。启动有丝分裂所需的蛋白激酶可防止DNA再次复制。当细胞退出有丝分裂时,细胞周期被重置,从而允许建立一个新的、有活性的复制状态。

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Cell cycle control of DNA replication.DNA复制的细胞周期调控
Science. 1996 Dec 6;274(5293):1659-64. doi: 10.1126/science.274.5293.1659.
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Assembly of a complex containing Cdc45p, replication protein A, and Mcm2p at replication origins controlled by S-phase cyclin-dependent kinases and Cdc7p-Dbf4p kinase.由S期细胞周期蛋白依赖性激酶和Cdc7p-Dbf4p激酶控制,在复制起点组装包含Cdc45p、复制蛋白A和Mcm2p的复合物。
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