Liu Jinbao, Su Huabo, Wang Xuejun
a State Key Laboratory of Respiratory Disease and Department of Pathophysiology , Guangzhou Medical University , Guangzhou , Guangdong , China.
b Vascular Biology Center and Department of Pharmacology and Toxicology , Medical College of Georgia, Georgia Regents University , Augusta , GA , USA.
Autophagy. 2016;12(3):601-2. doi: 10.1080/15548627.2015.1136773.
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.
我们首次证明,COP9信号体(COPS)可能通过支持CUL/泛素连接酶介导的泛素化作用,控制心肌细胞胞质中替代型和真正的错误折叠蛋白的降解,并且Cops8基因低表达会加剧小鼠的心脏蛋白病,其中自噬功能受损似乎也在起作用。研究另一个Cops基因的心脏消融,以解读COPS8缺陷表型是归因于整个COPS还是COPS8所特有的,将极其重要。