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- Title
Regulation of with-no-lysine kinase signaling by Kelch-like proteins.
- Authors
Uchida, Shinichi; Sohara, Eisei; Rai, Tatemitsu; Sasaki, Sei
- Abstract
In 2001, with-no-lysine (WNK) kinases were identified as the genes responsible for the human hereditary hypertensive disease pseudohypoaldosteronism type II (PHAII). It took a further 6 years to clarify that WNK kinases participate in a signaling cascade with oxidative stress-responsive gene 1 (OSR1), Ste20-related proline-alanine-rich kinase (SPAK), and thiazide-sensitive NaCl cotransporter (NCC) in the kidney and the constitutive activation of this signaling cascade is the molecular basis of PHAII. Since this discovery, the WNK-OSR1/SPAK-NCC signaling cascade has been shown to be involved not only in PHAII but also in the regulation of blood pressure under normal and pathogenic conditions, such as hyperinsulinemia. However, the molecular mechanisms of WNK kinase regulation by dietary and hormonal factors and by PHAII-causing mutations remain poorly understood. In 2012, two additional genes responsible for PHAII, Kelch-like 3 ( KLHL3) and Cullin3, were identified. At the time of their discovery, the molecular mechanisms underlying the interaction between these genes and their involvement in PHAII were unknown. Here we review the pathophysiological roles of the WNK signaling cascade clarified to date and introduce a new mechanism of WNK kinase regulation by KLHL3 and Cullin3, which provides insight on previously unknown mechanisms of WNK kinase regulation.
- Subjects
LYSINE; PROTEIN kinases; HYPERTENSION; OXIDATIVE stress; GENETIC regulation; BLOOD pressure; HYPERINSULINISM
- Publication
Biology of the Cell (Wiley-Blackwell), 2014, Vol 106, Issue 2, p45
- ISSN
0248-4900
- Publication type
Article
- DOI
10.1111/boc.201300069