Machida Yuichi J, Machida Yuka, Vashisht Ajay A, Wohlschlegel James A, Dutta Anindya
Division of Oncology Research, Mayo College of Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.
J Biol Chem. 2009 Dec 4;284(49):34179-88. doi: 10.1074/jbc.M109.046755. Epub 2009 Oct 8.
The deubiquitinating enzyme BRCA1-associated protein 1 (BAP1) possesses growth inhibitory activity and functions as a tumor suppressor. In this study we report that BAP1 also plays positive roles in cell proliferation. BAP1 depletion by RNAi inhibits cell proliferation as does overexpression of a dominant negative mutant of BAP1. Mass spectrometry analyses of copurified proteins revealed that BAP1 is associated with factors involved in chromatin modulation and transcriptional regulation. We show that the interaction with host cell factor-1 (HCF-1), a cell-cycle regulator composed of HCF-1N and HCF-1C, is critical for the BAP1-mediated growth regulation. We found that HCF-1N is modified with Lys-48-linked polyubiquitin chains on its Kelch domain. The HCF-1 binding motif of BAP1 is required for interaction with HCF-1N and mediates deubiquitination of HCF-1N by BAP1. The importance of the BAP1-HCF-1 interaction is underscored by the fact that growth suppression by the dominant negative BAP1 mutant is entirely dependent on the HCF-1 binding motif. These results suggest that BAP1 regulates cell proliferation by deubiquitinating HCF-1.
去泛素化酶BRCA1相关蛋白1(BAP1)具有生长抑制活性,并作为一种肿瘤抑制因子发挥作用。在本研究中,我们报告BAP1在细胞增殖中也发挥着积极作用。通过RNA干扰使BAP1缺失会抑制细胞增殖,BAP1显性负性突变体的过表达也会产生同样的效果。对共纯化蛋白的质谱分析表明,BAP1与参与染色质调节和转录调控的因子相关。我们发现,与宿主细胞因子1(HCF-1,一种由HCF-1N和HCF-1C组成的细胞周期调节因子)的相互作用对于BAP1介导的生长调节至关重要。我们发现HCF-1N在其Kelch结构域上被赖氨酸48连接的多聚泛素链修饰。BAP1的HCF-1结合基序是与HCF-1N相互作用所必需的,并介导BAP1对HCF-1N的去泛素化作用。显性负性BAP1突变体的生长抑制作用完全依赖于HCF-1结合基序,这一事实突出了BAP1-HCF-1相互作用的重要性。这些结果表明,BAP1通过对HCF-1去泛素化来调节细胞增殖。