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Cdc20:在染色体分离和有丝分裂退出的十字路口。

Cdc20: At the Crossroads between Chromosome Segregation and Mitotic Exit.

机构信息

Faculty of Health and Life Sciences, Department of Biological and Medical Sciences, Oxford Brookes University, Oxford OX3 0BP, UK.

Faculty of Health and Life Sciences, Department of Biological and Medical Sciences, Oxford Brookes University, Oxford OX3 0BP, UK.

出版信息

Trends Biochem Sci. 2017 Mar;42(3):193-205. doi: 10.1016/j.tibs.2016.12.001. Epub 2017 Feb 12.

Abstract

Cell-division cycle protein 20 homologue (Cdc20) has important functions in chromosome segregation and mitotic exit. Cdc20 is the target of the spindle assembly checkpoint (SAC) and a key cofactor of the anaphase-promoting complex or cyclosome (APC/C) E3 ubiquitin ligase, thus regulating APC/C ubiquitin activity on specific substrates for their subsequent degradation by the proteasome. Here we discuss the roles of Cdc20 in SAC signalling and mitotic exit, describe how the integration of traditional approaches with emerging technologies has revealed new details of Cdc20 functions, comment about the potential of Cdc20 as a therapeutic target for the treatment of human malignancies, and discuss recent advances and controversies in the mechanistic understanding of the control of chromosome segregation during cell division.

摘要

细胞分裂周期蛋白 20 同源物(Cdc20)在染色体分离和有丝分裂后期中具有重要功能。Cdc20 是纺锤体组装检查点(SAC)的靶标,也是后期促进复合物或环体(APC/C)E3 泛素连接酶的关键辅助因子,从而调节 APC/C 对特定底物的泛素活性,以便随后通过蛋白酶体进行降解。在这里,我们讨论了 Cdc20 在 SAC 信号传导和有丝分裂后期中的作用,描述了如何将传统方法与新兴技术相结合,揭示了 Cdc20 功能的新细节,评论了 Cdc20 作为治疗人类恶性肿瘤的治疗靶标的潜力,并讨论了在细胞分裂过程中控制染色体分离的机制理解方面的最新进展和争议。

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