Koretke K K, Lupas A N, Warren P V, Rosenberg M, Brown J R
SmithKline Beecham Pharmaceuticals, Collegeville, Pennsylvania 19426-0989, USA.
Mol Biol Evol. 2000 Dec;17(12):1956-70. doi: 10.1093/oxfordjournals.molbev.a026297.
Two-component signal transduction (TCST) systems are the principal means for coordinating responses to environmental changes in bacteria as well as some plants, fungi, protozoa, and archaea. These systems typically consist of a receptor histidine kinase, which reacts to an extracellular signal by phosphorylating a cytoplasmic response regulator, causing a change in cellular behavior. Although several model systems, including sporulation and chemotaxis, have been extensively studied, the evolutionary relationships between specific TCST systems are not well understood, and the ancestry of the signal transduction components is unclear. Phylogenetic trees of TCST components from 14 complete and 6 partial genomes, containing 183 histidine kinases and 220 response regulators, were constructed using distance methods. The trees showed extensive congruence in the positions of 11 recognizable phylogenetic clusters. Eukaryotic sequences were found almost exclusively in one cluster, which also showed the greatest extent of domain variability in its component proteins, and archaeal sequences mainly formed species-specific clusters. Three clusters in different parts of the kinase tree contained proteins with serine-phosphorylating activity. All kinases were found to be monophyletic with respect to other members of their superfamily, such as type II topoisomerases and Hsp90. Structural analysis further revealed significant similarity to the ATP-binding domain of eukaryotic protein kinases. TCST systems are of bacterial origin and radiated into archaea and eukaryotes by lateral gene transfer. Their components show extensive coevolution, suggesting that recombination has not been a major factor in their differentiation. Although histidine kinase activity is prevalent, serine kinases have evolved multiple times independently within this family, accompanied by a loss of the cognate response regulator(s). The structural and functional similarity between TCST kinases and eukaryotic protein kinases raises the possibility of a distant evolutionary relationship.
双组分信号转导(TCST)系统是细菌以及一些植物、真菌、原生动物和古菌中协调对环境变化作出反应的主要方式。这些系统通常由一个受体组氨酸激酶组成,该激酶通过磷酸化细胞质响应调节因子对细胞外信号作出反应,从而引起细胞行为的改变。尽管包括芽孢形成和趋化性在内的几个模型系统已得到广泛研究,但特定TCST系统之间的进化关系尚不清楚,信号转导成分的起源也不明确。使用距离方法构建了来自14个完整基因组和6个部分基因组的TCST成分的系统发育树,其中包含183个组氨酸激酶和220个响应调节因子。这些树在11个可识别的系统发育簇的位置上显示出广泛的一致性。真核序列几乎只出现在一个簇中,该簇在其组成蛋白中也显示出最大程度的结构域变异性,而古菌序列主要形成物种特异性簇。激酶树不同部分的三个簇包含具有丝氨酸磷酸化活性的蛋白。发现所有激酶与其超家族的其他成员,如II型拓扑异构酶和Hsp90,是单系的。结构分析进一步揭示了与真核蛋白激酶的ATP结合结构域有显著相似性。TCST系统起源于细菌,并通过横向基因转移辐射到古菌和真核生物中。它们的成分显示出广泛的共同进化,这表明重组不是它们分化的主要因素。尽管组氨酸激酶活性普遍存在,但丝氨酸激酶在这个家族中丝氨酸激酶已多次独立进化,同时伴随着同源响应调节因子的丢失。TCST激酶与真核蛋白激酶之间的结构和功能相似性增加了它们存在遥远进化关系的可能性。