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SENP3 和 USP7 调节 Polycomb-rixosome 相互作用和沉默功能。

SENP3 and USP7 regulate Polycomb-rixosome interactions and silencing functions.

机构信息

Howard Hughes Medical Institute, Department of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA; National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.

Howard Hughes Medical Institute, Department of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Cell Rep. 2023 Apr 25;42(4):112339. doi: 10.1016/j.celrep.2023.112339. Epub 2023 Apr 3.

Abstract

The rixosome and PRC1 silencing complexes are associated with deSUMOylating and deubiquitinating enzymes, SENP3 and USP7, respectively. How deSUMOylation and deubiquitylation contribute to rixosome- and Polycomb-mediated silencing is not fully understood. Here, we show that the enzymatic activities of SENP3 and USP7 are required for silencing of Polycomb target genes. SENP3 deSUMOylates several rixosome subunits, and this activity is required for association of the rixosome with PRC1. USP7 associates with canonical PRC1 (cPRC1) and deubiquitinates the chromodomain subunits CBX2 and CBX4, and inhibition of USP activity results in disassembly of cPRC1. Finally, both SENP3 and USP7 are required for Polycomb- and rixosome-dependent silencing at an ectopic reporter locus. These findings demonstrate that SUMOylation and ubiquitination regulate the assembly and activities of the rixosome and Polycomb complexes and raise the possibility that these modifications provide regulatory mechanisms that may be utilized during development or in response to environmental challenges.

摘要

核糖体和 PRC1 沉默复合物分别与去 SUMO 化酶和去泛素化酶 SENP3 和 USP7 相关。去 SUMO 化和去泛素化如何促进核糖体和多梳复合物介导的沉默尚未完全阐明。在这里,我们表明 SENP3 和 USP7 的酶活性对于多梳靶基因的沉默是必需的。SENP3 去 SUMO 化几个核糖体亚基,这种活性对于核糖体与 PRC1 的结合是必需的。USP7 与典型的 PRC1(cPRC1)结合,并去泛素化 chromodomain 亚基 CBX2 和 CBX4,USP 活性的抑制导致 cPRC1 的解体。最后,SENP3 和 USP7 都需要在异位报告基因座上进行多梳和核糖体依赖性沉默。这些发现表明 SUMO 化和泛素化调节核糖体和多梳复合物的组装和活性,并提出这些修饰可能提供在发育过程中或响应环境挑战时可利用的调节机制的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbd9/10777863/74723f280fef/nihms-1954671-f0002.jpg

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