卡林
COP9信号体
细胞生物学
远曲小管
生物
化学
泛素
生物化学
内分泌学
基因
肾
泛素连接酶
酶
蛋白酶
肾单位
肽水解酶类
作者
Yujiro Maeoka,T R Bradford,Xiao-Tong Su,Avika Sharma,Chao Yang,David H. Ellison,James A. McCormick,Ryan J. Cornelius
出处
期刊:American Journal of Physiology-renal Physiology
[American Physiological Society]
日期:2024-08-29
标识
DOI:10.1152/ajprenal.00138.2024
摘要
The disease Familial Hyperkalemic Hypertension (FHHt; also known as Gordon Syndrome) is caused by aberrant accumulation of WNK4 activating the NaCl cotransporter (NCC) in the distal convoluted tubule (DCT) of the kidney. Mutations in cullin 3 (CUL3) cause FHHt by disrupting interaction with the deneddylase COP9 signalosome (CSN). Deletion of
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