Disease‐causing mutations in KLHL3 impair its effect on WNK4 degradation
Copyright policy )Disease‐causing mutations in KLHL3 impair its effect on WNK4 degradation
Mutations in with‐no‐lysine (K) kinase 4 (WNK4) and a ubiquitin E3 ligase complex component kelch‐like 3 (KLHL3) both cause pseudohypoaldosteronism II (PHAII), a hereditary form of hypertension. We determined whether WNK4 or its effector is regulated by KLHL3 in Xenopus oocytes. KLHL3 inhibited the positive effect of WNK4 on Na+–Cl− cotransporter (NCC) by decreasing WNK4 protein abundance without decreasing that of NCC and the downstream kinase OSR1 directly. Ubiquitination and degradation of WNK4 were induced by KLHL3. The effect of KLHL3 on WNK4 degradation was blocked by a dominant negative form of cullin 3. All five PHAII mutations of KLHL3 tested disrupted the regulation on WNK4. We conclude that KLHL3 is a substrate adaptor for WNK4 in a ubiquitin E3 ligase complex.
Ubiquitin E3 ligase, Symporters, Protein Stability, with-no-lysine (K) kinase 4, Pseudohypoaldosteronism, Receptors, Drug, Ubiquitin-Protein Ligases, Microfilament Proteins, Ubiquitination, Protein Serine-Threonine Kinases, Cullin Proteins, Mice, Cullin 3, Mutation, Proteolysis, Animals, Humans, Solute Carrier Family 12, Member 3, Carrier Proteins, kelch-like 3, Adaptor Proteins, Signal Transducing
Ubiquitin E3 ligase, Symporters, Protein Stability, with-no-lysine (K) kinase 4, Pseudohypoaldosteronism, Receptors, Drug, Ubiquitin-Protein Ligases, Microfilament Proteins, Ubiquitination, Protein Serine-Threonine Kinases, Cullin Proteins, Mice, Cullin 3, Mutation, Proteolysis, Animals, Humans, Solute Carrier Family 12, Member 3, Carrier Proteins, kelch-like 3, Adaptor Proteins, Signal Transducing
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