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通过蛋白质降解对转录因子进行调控。

Regulation of transcription factors by protein degradation.

作者信息

Desterro J M, Rodriguez M S, Hay R T

机构信息

School of Biology, University of St. Andrews, Fife, United Kingdom.

出版信息

Cell Mol Life Sci. 2000 Aug;57(8-9):1207-19. doi: 10.1007/pl00000760.

Abstract

The level of transcription factors is tightly controlled by their rates of synthesis and degradation. Many critical factors are maintained at an appropriate level by targeted addition of ubiquitin and degradation via the proteasome. Whereas ubiquitination targets modified proteins for degradation, modification of substrates by the family of ubiquitin-like proteins does not target the proteins for degradation but can alter the stability and other properties of the modified proteins. Here we discuss the elaborate mechanisms that have evolved to allow specific recognition of substrates targeted for modification. Specific examples are discussed to illustrate the different mechanisms involved and the importance of regulated degradation in diseases such as cancer.

摘要

转录因子的水平受到其合成和降解速率的严格控制。许多关键因子通过靶向添加泛素并经由蛋白酶体进行降解而维持在适当水平。泛素化作用将修饰后的蛋白质作为降解目标,而类泛素蛋白家族对底物的修饰并不将蛋白质作为降解目标,但可改变被修饰蛋白质的稳定性和其他特性。在此,我们讨论为实现对靶向修饰底物的特异性识别而演化出的精细机制。文中讨论了具体实例,以阐明所涉及的不同机制以及在诸如癌症等疾病中受调控降解的重要性。

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