Wade Ramon, Vande Pol Scott
Department of Pathology, University of Virginia, P.O. Box 800904, Charlottesville, VA 22908-0904, USA.
Biochem J. 2006 Jan 15;393(Pt 2):565-73. doi: 10.1042/BJ20051241.
Tyrosine phosphorylation of FAK (focal adhesion kinase) regulates signalling that results from the interaction of integrins with extracellular matrix and growth factor receptors. A critical step in this process is the phosphorylation of Tyr397 of FAK, which creates a binding site for Src family kinases, PI3K (phosphoinositide 3-kinase) and Shc (Src homology and collagen homology). An intact Tyr397 site is required for FAK-mediated regulation of cell migration, survival signals and full responsiveness to soluble growth factors. We showed previously that the adaptor protein paxillin is required for the overall tyrosine phosphorylation of FAK in embryonic stem cells [Wade, Bohl and Vande Pol (2002) Oncogene 21, 96-107]. In the present paper, we identify the minimal structural features of paxillin that are required to support overall FAK tyrosine phosphorylation and Tyr397 phosphorylation. Paxillin contains N-terminal leucine-rich LD motifs that bind directly to FAK and four LIM (Lin-11, Isl-1 and Mec-3) domains in the C-terminus. We show that paxillin LIM domains 1, 2 and 3 are each required for FAK tyrosine phosphorylation, while LIM4 is dispensable. In addition to paxillin LIM domains 1, 2 and 3, a single LD motif on paxillin is required to support FAK tyrosine phosphorylation in embryonic stem cells. Both sequence and spatial requirements exist for LD motifs to support FAK tyrosine phosphorylation. Interestingly, synthetic LD motifs that fail to bind FAK in vitro are able to fully support FAK tyrosine phosphorylation, indicating that minimal interactions of LD motifs with FAK suffice. Our results demonstrate at least four distinct structural domains of paxillin support at least three distinct functions that are each required for FAK tyrosine phosphorylation.
粘着斑激酶(FAK)的酪氨酸磷酸化调节着由整合素与细胞外基质及生长因子受体相互作用所产生的信号传导。这一过程中的关键步骤是FAK的Tyr397位点发生磷酸化,该位点会形成一个与Src家族激酶、磷脂酰肌醇3激酶(PI3K)及Shc(Src同源和胶原蛋白同源)结合的位点。FAK介导的细胞迁移调节、存活信号以及对可溶性生长因子的完全反应需要完整的Tyr397位点。我们之前表明衔接蛋白桩蛋白是胚胎干细胞中FAK整体酪氨酸磷酸化所必需的[韦德、博尔和万德·波尔(2002年)《癌基因》21卷,96 - 107页]。在本文中,我们确定了桩蛋白支持FAK整体酪氨酸磷酸化和Tyr397磷酸化所需的最小结构特征。桩蛋白包含直接与FAK结合的N端富含亮氨酸的LD基序以及C端的四个LIM(Lin - 11、Isl - 1和Mec - 3)结构域。我们发现桩蛋白的LIM结构域1、2和3各自都是FAK酪氨酸磷酸化所必需的,而LIM4则是可有可无的。除了桩蛋白的LIM结构域1、2和3外,桩蛋白上单个的LD基序对于支持胚胎干细胞中的FAK酪氨酸磷酸化也是必需的。LD基序支持FAK酪氨酸磷酸化存在序列和空间要求。有趣的是,在体外无法与FAK结合的合成LD基序能够完全支持FAK酪氨酸磷酸化,这表明LD基序与FAK的最小相互作用就足够了。我们的结果表明,桩蛋白至少四个不同的结构域支持FAK酪氨酸磷酸化所需的至少三种不同功能。