Department of Molecular Pharmacology and Therapeutics, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois 60153, USA.
J Biol Chem. 2010 Mar 5;285(10):6970-9. doi: 10.1074/jbc.M109.083642. Epub 2010 Jan 4.
Previously we showed that the inactive form of p90 ribosomal S6 kinase 1 (RSK1) interacts with the regulatory subunit, PKARIalpha, of protein kinase A (PKA), whereas the active RSK1 interacts with the catalytic subunit (PKAc) of PKA. Herein, we demonstrate that the N-terminal kinase domain (NTK) of RSK1 is necessary for interactions with PKARIalpha. Substitution of the activation loop phosphorylation site (Ser-221) in the NTK with the negatively charged Asp residue abrogated the association between RSK1 and PKARIalpha. This explains the lack of an interaction between active RSK1 and PKARIalpha. Full-length RSK1 bound to PKARIalpha with an affinity of 0.8 nm. The NTK domain of RSK1 competed with PKAc for binding to the pseudosubstrate region (amino acids 93-99) of PKARIalpha. Overexpressed RSK1 dissociated PKAc from PKARIalpha, increasing PKAc activity, whereas silencing of RSK1 increased PKAc/PKARIalpha interactions and decreased PKAc activity. Unlike PKAc, which requires Arg-95 and -96 in the pseudosubstrate region of PKARIalpha for their interactions, RSK1/PKARIalpha association requires all four Arg residues (Arg-93-96) in the pseudosubstrate site of PKARIalpha. A peptide (Wt-PS) corresponding to residues 91-99 of PKARIalpha competed for binding of RSK1 with PKARIalpha both in vitro and in intact cells. Furthermore, peptide Wt-PS (but not control peptide Mut-PS), by dissociating RSK1 from PKARIalpha, activated RSK1 in the absence of any growth factors and protected cells from apoptosis. Thus, by competing for binding to the pseudosubstrate region of PKARIalpha, RSK1 regulates PKAc activity in a cAMP-independent manner, and PKARIalpha by associating with RSK1 regulates its activation and its biological functions.
先前我们表明,无活性的核糖体 S6 激酶 1(RSK1)与蛋白激酶 A(PKA)的调节亚基 PKARIα相互作用,而活性的 RSK1 与 PKA 的催化亚基(PKAc)相互作用。在此,我们证明 RSK1 的 N 端激酶结构域(NTK)对于与 PKARIα 的相互作用是必需的。在 NTK 中的激活环磷酸化位点(Ser-221)被带负电荷的 Asp 残基取代后,RSK1 与 PKARIα 的关联被消除。这解释了活性 RSK1 与 PKARIα 之间缺乏相互作用的原因。全长的 RSK1 与 PKARIα 的亲和力为 0.8nm。RSK1 的 NTK 结构域与 PKAc 竞争结合 PKARIα 的假底物区域(氨基酸 93-99)。过表达的 RSK1 将 PKAc 从 PKARIα 上解离下来,增加了 PKAc 的活性,而 RSK1 的沉默增加了 PKAc/PKARIα 的相互作用,降低了 PKAc 的活性。与需要 PKARIα 的假底物区域中的 Arg-95 和 Arg-96 来与 PKAc 相互作用不同,RSK1/PKARIα 的相互作用需要 PKARIα 的假底物位点中的所有四个 Arg 残基(Arg-93-96)。与 PKARIα 的 91-99 位残基相对应的肽(Wt-PS)在体外和完整细胞中均与 RSK1 竞争结合 PKARIα。此外,肽 Wt-PS(而不是对照肽 Mut-PS)通过将 RSK1 从 PKARIα 上解离下来,在没有任何生长因子的情况下激活 RSK1,并保护细胞免受凋亡。因此,RSK1 通过与 PKARIα 的假底物区域竞争结合来调节 PKAc 的活性,而与 RSK1 结合的 PKARIα 则调节其自身的激活及其生物学功能。