Xu Bing E, Lee Byung Hoon, Min Xiaoshan, Lenertz Lisa, Heise Charles J, Stippec Steve, Goldsmith Elizabeth J, Cobb Melanie H
Department of Pharmacology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX, USA.
Cell Res. 2005 Jan;15(1):6-10. doi: 10.1038/sj.cr.7290256.
The WNK kinases are a recently discovered family of serine-threonine kinases that have been shown to play an essential role in the regulation of electrolyte homeostasis. Intronic deletions in the WNK1 gene result in its overexpression and lead to pseudohypoaldosteronism type II, a disease with salt-sensitive hypertension and hyperkalemia. This review focuses on the recent evidence elucidating the structure of the kinase domain of WNK1 and functions of these kinases in normal and disease physiology. Their functions have implications for understanding the biochemical mechanism that could lead to the retention or insertion of proteins in the plasma membrane. The WNK kinases may be able to influence ion homeostasis through its effects on synaptotagmin function.
WNK激酶是最近发现的丝氨酸-苏氨酸激酶家族,已被证明在电解质稳态调节中起重要作用。WNK1基因的内含子缺失导致其过度表达,并导致II型假性醛固酮增多症,这是一种伴有盐敏感性高血压和高钾血症的疾病。本综述重点关注阐明WNK1激酶结构域结构及其在正常和疾病生理学中功能的最新证据。它们的功能对于理解可能导致蛋白质在质膜中保留或插入的生化机制具有重要意义。WNK激酶可能通过对突触结合蛋白功能的影响来影响离子稳态。