National Key Laboratory of Agricultural Microbiology, Center for Proteomics Research, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, China.
J Bacteriol. 2010 Apr;192(7):1956-64. doi: 10.1128/JB.01471-09. Epub 2010 Jan 29.
Protein phosphorylation plays an important role in cell signaling. However, in the Archaea, little is known about which proteins are phosphorylated and which kinases are involved. In this study, we identified, for the first time, a typical eukaryote-like Ser/Thr protein kinase and its protein partner, a forkhead-associated (FHA)-domain-containing protein, from the archaeon Sulfolobus tokodaii strain 7. This protein kinase, ST1565, physically interacted with the FHA-domain-containing protein, ST0829, both in vivo and in vitro. ST1565 preferred Mn(2+) as a cofactor for autophosphorylation and for substrate phosphorylation; the optimal temperature for this was 45 degrees C, and the optimal pH was 5.5 to 7.5. The critical amino acid residues of the conserved FHA and kinase domain sites were identified by performing a series of mutation assays. Thr329 was part of a major activation site in the kinase, while Thr326 was a negative regulation site. Several mutants with amino acid substitutions in the conserved FHA domain sites of ST0829 did not physically interact with ST1565. A structural model for the FHA domain demonstrated that the mutation sites were located at the edge of the protein and thus were in the domain that potentially interacts with ST1565. This report describes pioneering work on the third domain of life, the Archaea, showing that a protein kinase interacts with and phosphorylates an FHA-domain-containing protein. Our data provide critical information on the structural or functional characteristics of archaeal proteins and could help increase our understanding of fundamental signaling mechanisms in all three domains of life.
蛋白质磷酸化在细胞信号转导中起着重要作用。然而,在古菌中,人们对哪些蛋白质被磷酸化以及涉及哪些激酶知之甚少。在这项研究中,我们首次从古菌 Sulfolobus tokodaii 株 7 中鉴定出一种典型的真核样丝氨酸/苏氨酸蛋白激酶及其蛋白伴侣叉头相关(FHA)结构域蛋白。这种蛋白激酶 ST1565 与 FHA 结构域蛋白 ST0829 在体内和体外均相互作用。ST1565 更喜欢 Mn(2+)作为自磷酸化和底物磷酸化的辅助因子;最适温度为 45 度,最适 pH 值为 5.5 至 7.5。通过进行一系列突变实验鉴定了保守 FHA 和激酶结构域位点的关键氨基酸残基。Thr329 是激酶中主要激活位点的一部分,而 Thr326 是负调控位点。在 ST0829 的保守 FHA 结构域位点进行氨基酸取代的几个突变体没有与 ST1565 发生物理相互作用。ST0829 的 FHA 结构域的结构模型表明,突变位点位于蛋白质的边缘,因此位于可能与 ST1565 相互作用的结构域。本报告描述了针对生命的第三领域——古菌的开创性工作,表明蛋白激酶与 FHA 结构域蛋白相互作用并磷酸化该蛋白。我们的数据提供了有关古菌蛋白结构或功能特征的关键信息,并有助于提高我们对所有三个生命领域基本信号机制的理解。