Cohn Martin A, Kee Younghoon, Haas Wilhelm, Gygi Steven P, D'Andrea Alan D
Department of Radiation Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Biol Chem. 2009 Feb 20;284(8):5343-51. doi: 10.1074/jbc.M808430200. Epub 2008 Dec 15.
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.
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。