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通过蛋白质降解进行细胞周期调控。

Cell cycle regulation by protein degradation.

作者信息

Koepp Deanna M

机构信息

Department of Genetics, Cell Biology and Development, University of Minnesota, 6-160 Jackson Hall, 321 Church St SE, Minneapolis, MN, 55455, USA,

出版信息

Methods Mol Biol. 2014;1170:61-73. doi: 10.1007/978-1-4939-0888-2_4.

Abstract

Cell division is controlled by a highly regulated program to accurately duplicate and segregate chromosomes. An important feature of the cell cycle regulatory program is that key cell cycle proteins are present and active during specific cell cycle stages but are later removed or inhibited to maintain appropriate timing. The ubiquitin-proteasome system has emerged as an important mechanism to target cell cycle proteins for degradation at critical junctures during cell division. Two key E3 ubiquitin ligase complexes that target key cell cycle proteins are the Skp1-Cul1-F-box protein complex and the anaphase-promoting complex/cyclosome. This chapter focuses on the role of these E3 ubiquitin ligases and how ubiquitin-dependent degradation of central cell cycle regulatory proteins advances the cell cycle.

摘要

细胞分裂受高度调控的程序控制,以精确复制和分离染色体。细胞周期调控程序的一个重要特征是关键的细胞周期蛋白在特定的细胞周期阶段存在并发挥作用,但随后会被去除或抑制,以维持适当的时间安排。泛素-蛋白酶体系统已成为在细胞分裂过程中的关键节点将细胞周期蛋白靶向降解的重要机制。靶向关键细胞周期蛋白的两个关键E3泛素连接酶复合物是Skp1-Cul1-F-box蛋白复合物和后期促进复合物/细胞周期体。本章重点关注这些E3泛素连接酶的作用,以及核心细胞周期调节蛋白的泛素依赖性降解如何推动细胞周期进程。

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