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真核生物DNA复制:多亚基蛋白复合物的协同作用。

Eukaryotic DNA replication: Orchestrated action of multi-subunit protein complexes.

作者信息

Kang Sukhyun, Kang Mi-Sun, Ryu Eunjin, Myung Kyungjae

机构信息

Center for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.

Center for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.

出版信息

Mutat Res. 2018 May;809:58-69. doi: 10.1016/j.mrfmmm.2017.04.002. Epub 2017 May 1.

Abstract

Genome duplication is an essential process to preserve genetic information between generations. The eukaryotic cell cycle is composed of functionally distinct phases: G1, S, G2, and M. One of the key replicative proteins that participate at every stage of DNA replication is the Mcm2-7 complex, a replicative helicase. In the G1 phase, inactive Mcm2-7 complexes are loaded on the replication origins by replication-initiator proteins, ORC and Cdc6. Two kinases, S-CDK and DDK, convert the inactive origin-loaded Mcm2-7 complex to an active helicase, the CMG complex in the S phase. The activated CMG complex begins DNA unwinding and recruits enzymes essential for DNA synthesis to assemble a replisome at the replication fork. After completion of DNA synthesis, the inactive CMG complex on the replicated DNA is removed from chromatin to terminate DNA replication. In this review, we will discuss the structure, function, and regulation of the molecular machines involved in each step of DNA replication.

摘要

基因组复制是在代与代之间保存遗传信息的一个重要过程。真核细胞周期由功能不同的阶段组成:G1期、S期、G2期和M期。参与DNA复制每个阶段的关键复制蛋白之一是Mcm2-7复合物,一种复制解旋酶。在G1期,无活性的Mcm2-7复合物由复制起始蛋白ORC和Cdc6加载到复制起点上。两种激酶,S-CDK和DDK,将加载在起点上的无活性Mcm2-7复合物转化为活性解旋酶,即S期的CMG复合物。活化的CMG复合物开始解开DNA,并招募DNA合成所必需的酶,在复制叉处组装一个复制体。DNA合成完成后,复制DNA上的无活性CMG复合物从染色质上移除,以终止DNA复制。在这篇综述中,我们将讨论参与DNA复制每个步骤的分子机器的结构、功能和调控。

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