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泛素途径对细胞周期的调控。

Cell cycle regulation by the ubiquitin pathway.

作者信息

Pagano M

机构信息

Department of Pathology and Kaplan Cancer Center, New York University Medical Center, New York 10016, USA.

出版信息

FASEB J. 1997 Nov;11(13):1067-75. doi: 10.1096/fasebj.11.13.9367342.

Abstract

In the past 2 years, two ubiquitin-dependent proteolytic pathways have been established as important players in the regulation of the cell division cycle. In S. cerevisiae, the entry into S phase requires ubiquitin-mediated degradation of a cdk inhibitor, p40Sic1, in a pathway that involves the E2 enzyme Cdc34. Recent studies reviewed herein show that the Cdc34 pathway targets phosphorylated substrates. A second pathway that regulates chromosome segregation and mitotic exit by degrading anaphase inhibitors and mitotic cyclins involves a different E2 and a large molecular weight E3 complex, called the anaphase-promoting complex or cyclosome. This pathway targets substrates containing one or more destruction box motif.

摘要

在过去两年中,两条泛素依赖性蛋白水解途径已被确立为细胞分裂周期调控中的重要参与者。在酿酒酵母中,进入S期需要泛素介导的细胞周期蛋白依赖性激酶(cdk)抑制剂p40Sic1的降解,该途径涉及E2酶Cdc34。本文综述的最新研究表明,Cdc34途径靶向磷酸化底物。第二条途径通过降解后期抑制剂和有丝分裂周期蛋白来调节染色体分离和有丝分裂退出,该途径涉及一种不同的E2和一种称为后期促进复合物或细胞周期体的大分子E3复合物。该途径靶向含有一个或多个破坏框基序的底物。

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