Konishi H, Matsuzaki H, Tanaka M, Ono Y, Tokunaga C, Kuroda S, Kikkawa U
Biosignal Research Center, Kobe University, Japan.
Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7639-43. doi: 10.1073/pnas.93.15.7639.
RAC protein kinase (RAC-PK), a serine/threonine protein kinase containing a pleckstrin homology (PH) domain, was activated by cellular stress such as heat shock and hyperosmolarity. Wortmannin, which is known as a potent inhibitor of phosphatidylinositol 3-kinase and normally inhibits growth factor-induced activation of RAC-PK, did not suppress heat-shock induced activation of RAC-PK, indicating that this stress-induced activation of the kinase is not mediated by phosphatidylinositol 3-kinase. The PH domain was indispensable for stress-induced activation of RAC PK. In heat-treated cells, PKC delta, a member of the protein kinase C family, was found to associate with the PH domain of RAC-PK. This PKC subspecies was phosphorylated in vitro by RAC-PK. The results suggest that RAC-PK may play a role in the cellular response to stress through its PH domain.
RAC蛋白激酶(RAC-PK)是一种含有普列克底物蛋白同源(PH)结构域的丝氨酸/苏氨酸蛋白激酶,可被热休克和高渗等细胞应激激活。渥曼青霉素是一种已知的磷脂酰肌醇3激酶强效抑制剂,通常可抑制生长因子诱导的RAC-PK激活,但它并不能抑制热休克诱导的RAC-PK激活,这表明激酶的这种应激诱导激活不是由磷脂酰肌醇3激酶介导的。PH结构域对于RAC PK的应激诱导激活是必不可少的。在热处理细胞中,发现蛋白激酶C家族成员PKCδ与RAC-PK的PH结构域相关联。该PKC亚型在体外被RAC-PK磷酸化。结果表明,RAC-PK可能通过其PH结构域在细胞应激反应中发挥作用。