Suisse Annabelle, He DanQing, Legent Kevin, Treisman Jessica E
Helen L. and Martin S. Kimmel Center at the Skirball Institute for Biomolecular Medicine and Department of Cell Biology, NYU School of Medicine, 540 First Avenue, New York, NY 10016, USA.
Helen L. and Martin S. Kimmel Center at the Skirball Institute for Biomolecular Medicine and Department of Cell Biology, NYU School of Medicine, 540 First Avenue, New York, NY 10016, USA
Development. 2017 Jul 15;144(14):2673-2682. doi: 10.1242/dev.148767. Epub 2017 Jun 15.
The COP9 signalosome removes Nedd8 modifications from the Cullin subunits of ubiquitin ligase complexes, reducing their activity. Here, we show that mutations in the () gene increase the activity of ubiquitin ligases that contain Cullin 1. Analysis of mutant phenotypes revealed a requirement for the COP9 signalosome to prevent ectopic expression of Epidermal growth factor receptor (EGFR) target genes. It does so by protecting Capicua, a transcriptional repressor of EGFR target genes, from EGFR pathway-dependent ubiquitylation by a Cullin 1/SKP1-related A/Archipelago E3 ligase and subsequent proteasomal degradation. The CSN1b subunit also maintains basal Capicua levels by protecting it from a separate mechanism of degradation that is independent of EGFR signaling. As a suppressor of tumor growth and metastasis, Capicua may be an important target of the COP9 signalosome in cancer.
COP9信号体从泛素连接酶复合物的Cullin亚基上去除Nedd8修饰,从而降低其活性。在此,我们表明()基因中的突变会增加含有Cullin 1的泛素连接酶的活性。对突变体表型的分析揭示了COP9信号体对于防止表皮生长因子受体(EGFR)靶基因的异位表达是必需的。它通过保护Capicua(一种EGFR靶基因的转录抑制因子)免受Cullin 1 / SKP1相关A / Archipelago E3连接酶介导的EGFR途径依赖性泛素化及随后的蛋白酶体降解来实现这一点。CSN1b亚基还通过保护Capicua免受独立于EGFR信号传导的另一种降解机制的影响来维持其基础水平。作为肿瘤生长和转移的抑制因子,Capicua可能是COP9信号体在癌症中的一个重要靶点。