Zak Taylor J, Koshman Yevgenia E, Samarel Allen M, Robia Seth L
Department of Cell and Molecular Physiology and ‡Department of Medicine, Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago , Maywood, Illinois 60153, United States.
Biochemistry. 2017 Sep 5;56(35):4722-4731. doi: 10.1021/acs.biochem.7b00616. Epub 2017 Aug 23.
Focal adhesion kinase (FAK) plays a key role in integrin and growth factor signaling pathways. FAK-related non-kinase (FRNK) is an endogenous inhibitor of FAK that shares its primary structure with the C-terminal third of FAK. FAK S910 phosphorylation is known to regulate FAK protein-protein interactions, but the role of the equivalent site on FRNK (S217) is unknown. Here we determined that S217 is highly phosphorylated by ERK in cultured rat aortic smooth muscle cells. Blocking phosphorylation by mutation (S217A) greatly increased FRNK inhibitory potency, resulting in strong inhibition of FAK autophosphorylation at Y397 and induction of smooth muscle cell apoptosis. FRNK has been proposed to compete for FAK anchoring sites in focal adhesions, but we did not detect displacement of FAK by WT-FRNK or superinhibitory S217A-FRNK. Instead, we found FRNK interacted directly with FAK, and this interaction is markedly strengthened for the superinhibitory S217A-FRNK. The results suggest that FRNK limits growth and survival signaling pathways by binding directly to FAK in an inhibitory complex, and this inhibition is relieved by phosphorylation of FRNK at S217.
粘着斑激酶(FAK)在整合素和生长因子信号通路中起关键作用。FAK相关非激酶(FRNK)是FAK的一种内源性抑制剂,其一级结构与FAK C端的三分之一相同。已知FAK S910磷酸化可调节FAK蛋白-蛋白相互作用,但FRNK上等效位点(S217)的作用尚不清楚。在此,我们确定在培养的大鼠主动脉平滑肌细胞中,S217被ERK高度磷酸化。通过突变(S217A)阻断磷酸化可大大增强FRNK的抑制效力,导致对Y397处FAK自磷酸化的强烈抑制并诱导平滑肌细胞凋亡。有人提出FRNK可竞争粘着斑中FAK的锚定位点,但我们未检测到野生型FRNK或超抑制性S217A-FRNK对FAK的置换。相反,我们发现FRNK直接与FAK相互作用,并且这种相互作用在超抑制性S217A-FRNK中明显增强。结果表明,FRNK通过在抑制复合物中直接与FAK结合来限制生长和生存信号通路,并且S217处FRNK的磷酸化可解除这种抑制作用。