COP9信号体
生物
泛素
自噬
蛋白酶体
细胞生物学
蛋白质降解
卡林
基因
遗传学
泛素连接酶
生物化学
细胞凋亡
蛋白酶
肽水解酶类
酶
作者
Jinbao Liu,Huabo Su,Xuejun Wang
出处
期刊:Autophagy
[Taylor & Francis]
日期:2016-01-13
卷期号:12 (3): 601-602
被引量:7
标识
DOI:10.1080/15548627.2015.1136773
摘要
We demonstrated for the first time that the COP9 signalosome (COPS) controls the degradation of a surrogate and a bona fide misfolded protein in the cytosol of cardiomyocytes likely via supporting ubiquitination by CUL/cullin-RING ligases, and that Cops8 hypomorphism exacerbates cardiac proteinopathy in mice, in which autophagic impairment appears to be in play. It will be extremely imprtant to investigate cardiac ablation of another Cops gene to decipher whether COPS8 deficiency phenotypes are attributable to the COPS or unique to COPS8.
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