Suppr超能文献

UAF1是多种去泛素化酶复合物的一个亚基。

UAF1 is a subunit of multiple deubiquitinating enzyme complexes.

作者信息

Cohn Martin A, Kee Younghoon, Haas Wilhelm, Gygi Steven P, D'Andrea Alan D

机构信息

Department of Radiation Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Biol Chem. 2009 Feb 20;284(8):5343-51. doi: 10.1074/jbc.M808430200. Epub 2008 Dec 15.

Abstract

A balance between ubiquitination and deubiquitination regulates numerous cellular processes and pathways, and specific deubiquitinating enzymes often play the decisive role of controlling this balance. We recently reported that the USP1 deubiquitinating enzyme, which regulates the Fanconi anemia pathway by deubiquitinating the central player of the pathway, FANCD2, is activated by the WD40-repeat containing UAF1 protein through formation of a stable USP1/UAF1 protein complex. Here we present the isolation of two novel multisubunit deubiquitinating enzyme complexes containing USP12 and USP46, respectively. Both complexes contain the UAF1 protein as a bona fide subunit. Interestingly, UAF1 regulates the enzymatic activity of both enzyme complexes, suggesting that this activator protein may regulate a subclass of human deubiquitinating enzymes. We postulate that additional WD40-containing proteins may also form complexes with other human deubiquitinating enzymes and thereby regulate their activity and substrate specificity.

摘要

泛素化与去泛素化之间的平衡调节着众多细胞过程和信号通路,特定的去泛素化酶常常在控制这种平衡中起决定性作用。我们最近报道,USP1去泛素化酶通过去泛素化范可尼贫血通路的核心蛋白FANCD2来调节该通路,它通过与含WD40重复序列的UAF1蛋白形成稳定的USP1/UAF1蛋白复合物而被激活。在此,我们分别展示了两种新型多亚基去泛素化酶复合物的分离,它们分别含有USP12和USP46。两种复合物均含有UAF1蛋白作为真正的亚基。有趣的是,UAF1调节这两种酶复合物的酶活性,这表明这种激活蛋白可能调节人类去泛素化酶的一个亚类。我们推测,其他含WD40的蛋白也可能与其他人类去泛素化酶形成复合物,从而调节它们的活性和底物特异性。

相似文献

1
UAF1 is a subunit of multiple deubiquitinating enzyme complexes.UAF1是多种去泛素化酶复合物的一个亚基。
J Biol Chem. 2009 Feb 20;284(8):5343-51. doi: 10.1074/jbc.M808430200. Epub 2008 Dec 15.
5
Structural basis of FANCD2 deubiquitination by USP1-UAF1.USP1-UAF1 介导的 FANCD2 去泛素化的结构基础。
Nat Struct Mol Biol. 2021 Apr;28(4):356-364. doi: 10.1038/s41594-021-00576-8. Epub 2021 Apr 1.

引用本文的文献

6
ATAD5 functions as a regulatory platform for Ub-PCNA deubiquitination.ATAD5 作为 Ub-PCNA 去泛素化的调控平台发挥作用。
Proc Natl Acad Sci U S A. 2024 Aug 20;121(34):e2315759121. doi: 10.1073/pnas.2315759121. Epub 2024 Aug 15.

本文引用的文献

2
Protein partners of deubiquitinating enzymes.去泛素化酶的蛋白质伴侣。
Biochem J. 2008 Sep 1;414(2):161-75. doi: 10.1042/BJ20080798.
3
Histone ubiquitination: triggering gene activity.组蛋白泛素化:触发基因活性。
Mol Cell. 2008 Mar 28;29(6):653-63. doi: 10.1016/j.molcel.2008.02.014.
5
Launching a ubiquitination cascade at DNA breaks.在DNA断裂处启动泛素化级联反应。
Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20645-6. doi: 10.1073/pnas.0710916105. Epub 2007 Dec 19.
8
DUBA: a deubiquitinase that regulates type I interferon production.DUBA:一种调节I型干扰素产生的去泛素化酶。
Science. 2007 Dec 7;318(5856):1628-32. doi: 10.1126/science.1145918. Epub 2007 Nov 8.
10
A proteasome for all occasions.适用于各种情况的蛋白酶体。
FEBS Lett. 2007 Jun 19;581(15):2854-61. doi: 10.1016/j.febslet.2007.03.053. Epub 2007 Mar 30.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验