Ihara K, Umemura T, Katagiri I, Kitajima-Ihara T, Sugiyama Y, Kimura Y, Mukohata Y
Division of Biological Science Graduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
J Mol Biol. 1999 Jan 8;285(1):163-74. doi: 10.1006/jmbi.1998.2286.
The amino acid sequences of 25 archaeal retinal proteins from 13 different strains of extreme halophiles were analyzed to establish their molecular phylogenetic relationship. On the basis of amino acid sequence similarity, these proteins apparently formed a distinct family designated as the archaeal rhodopsin family (ARF), which was not related to other known proteins, including G protein-coupled receptors. The archaeal rhodopsin family was further divided into four clusters with different functions; H+ pump (bacteriorhodopsin), Cl- pump (halorhodopsin), and two kinds of sensor (sensory rhodopsin and phoborhodopsin). These four rhodopsin clusters seemed to have occurred by gene duplication(s) before the generic speciation of halophilic archaea, based on phylogenetic analysis. Therefore, the degrees of differences in amino acid sequences within each cluster simply reflected the divergent evolution of halophilic archaea. By comparing the branch lengths after speciation points of the reconstituted tree, we calculated the relative evolution rates of the four archaeal rhodopsins bacteriorhodopsin:halorhodopsin:sensory rhodopsin: phoborhodopsin to be 5:4:3:10. From these values, the degrees of functional and structural restriction of each protein can be inferred. The branching topology of four clusters grouped bacteriorhodopsin and halorhodopsin versus sensory rhodopsin and phoborhodopsin by likelihood mapping. Using bacteriorhodopsin (and halorhodopsin) as an outgroup, the gene duplication point of sensory rhodopsin/phoborhodopsin was determined. By calculating the branch lengths between the gene duplication point and each halophilic archaea speciation point, we could speculate upon the relative evolution rate of pre-sensory rhodopsin and pre-phoborhodopsin. The evolution rate of pre-sensory rhodopsin was fivefold faster than that of pre-phoborhodopsin, which suggests that the original function of the ancestral sensor was similar to that of phoborhodopsin, and that sensory rhodopsin evolved from pre-sensory rhodopsin by the accumulation of mutations. The changes in evolution rate by gene duplication and functional differentiation were demonstrated in the archaeal rhodopsin family using the gene duplication date and halobacterial speciation date as common time stamps.
分析了来自13种不同极端嗜盐菌菌株的25种古菌视黄醛蛋白的氨基酸序列,以确定它们的分子系统发育关系。基于氨基酸序列相似性,这些蛋白显然形成了一个独特的家族,称为古菌视紫红质家族(ARF),它与其他已知蛋白无关,包括G蛋白偶联受体。古菌视紫红质家族进一步分为四个具有不同功能的簇;H⁺泵(细菌视紫红质)、Cl⁻泵(嗜盐视紫红质)和两种传感器(感官视紫红质和避光视紫红质)。基于系统发育分析,这四个视紫红质簇似乎是在嗜盐古菌的物种形成之前通过基因复制产生的。因此,每个簇内氨基酸序列的差异程度简单地反映了嗜盐古菌的趋异进化。通过比较重建树中物种形成点之后的分支长度,我们计算出四种古菌视紫红质细菌视紫红质:嗜盐视紫红质:感官视紫红质:避光视紫红质的相对进化速率为5:4:3:10。从这些值可以推断出每种蛋白质的功能和结构限制程度。通过似然性映射,四个簇的分支拓扑将细菌视紫红质和嗜盐视紫红质与感官视紫红质和避光视紫红质分组。以细菌视紫红质(和嗜盐视紫红质)作为外类群,确定了感官视紫红质/避光视紫红质的基因复制点。通过计算基因复制点与每个嗜盐古菌物种形成点之间的分支长度,我们可以推测前感官视紫红质和前避光视紫红质的相对进化速率。前感官视紫红质的进化速率比前避光视紫红质快五倍,这表明祖先传感器的原始功能与避光视紫红质相似,并且感官视紫红质是通过突变积累从前感官视紫红质进化而来的。利用基因复制日期和嗜盐细菌物种形成日期作为共同时间标记,在古菌视紫红质家族中证明了基因复制和功能分化导致的进化速率变化。