Hu C D, Kariya K, Okada T, Qi X, Song C, Kataoka T
Department of Physiology II, Kobe University School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
J Biol Chem. 1999 Jan 1;274(1):48-51. doi: 10.1074/jbc.274.1.48.
Rap1A is phosphorylated by cAMP-dependent protein kinase (PKA), and this phosphorylation has been shown to modulate its interaction with other proteins. However, it is not known whether Rap1A phosphorylation is involved in regulation of its cellular functions, including suppression of Ras-dependent Raf-1 activation. We have previously shown that this suppressive activity of Rap1A is attributable to its greatly enhanced ability to bind to the cysteine-rich region (CRR, residues 152-184) of Raf-1 compared with that of Ras. Here, we show that phosphorylation of Rap1A by PKA abolished its binding activity to CRR. Furthermore, a mutant Rap1A(S180E), whose sole PKA phosphorylation residue, Ser-180, was substituted by an acidic residue, Glu, to mimic its phosphorylated form, failed to suppress Ras-dependent Raf-1 activation in COS-7 cells. These results indicate that the CRR binding activity and the Ras-suppressive function of Rap1A can be modulated through phosphorylation and suggest that Rap1A may function as a PKA-dependent regulator of Raf-1 activation, not merely as a suppressor.
Rap1A 被环磷酸腺苷(cAMP)依赖性蛋白激酶(PKA)磷酸化,且这种磷酸化已被证明可调节其与其他蛋白质的相互作用。然而,尚不清楚 Rap1A 的磷酸化是否参与其细胞功能的调节,包括对 Ras 依赖性 Raf-1 激活的抑制。我们之前已经表明,Rap1A 的这种抑制活性归因于其与 Ras 相比,与 Raf-1 的富含半胱氨酸区域(CRR,第 152 - 184 位氨基酸残基)结合能力的大幅增强。在此,我们表明 PKA 介导的 Rap1A 磷酸化消除了其与 CRR 的结合活性。此外,一种突变型 Rap1A(S180E),其唯一的 PKA 磷酸化位点 Ser-180 被酸性氨基酸 Glu 取代,以模拟其磷酸化形式,在 COS-7 细胞中未能抑制 Ras 依赖性 Raf-1 的激活。这些结果表明,Rap1A 的 CRR 结合活性和 Ras 抑制功能可通过磷酸化进行调节,并提示 Rap1A 可能作为 Raf-1 激活的 PKA 依赖性调节因子发挥作用,而不仅仅是作为抑制剂。