Brown J R, Doolittle W F
Canadian Institute for Advanced Research, Department of Biochemistry, Dalhousie University, Halifax, NS.
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2441-5. doi: 10.1073/pnas.92.7.2441.
Universal trees based on sequences of single gene homologs cannot be rooted. Iwabe et al. [Iwabe, N., Kuma, K.-I., Hasegawa, M., Osawa, S. & Miyata, T. (1989) Proc. Natl. Acad. Sci. USA 86, 9355-9359] circumvented this problem by using ancient gene duplications that predated the last common ancestor of all living things. Their separate, reciprocally rooted gene trees for elongation factors and ATPase subunits showed Bacteria (eubacteria) as branching first from the universal tree with Archaea (archaebacteria) and Eucarya (eukaryotes) as sister groups. Given its topical importance to evolutionary biology and concerns about the appropriateness of the ATPase data set, an evaluation of the universal tree root using other ancient gene duplications is essential. In this study, we derive a rooting for the universal tree using aminoacyl-tRNA synthetase genes, an extensive multigene family whose divergence likely preceded that of prokaryotes and eukaryotes. An approximately 1600-bp conserved region was sequenced from the isoleucyl-tRNA synthetases of several species representing deep evolutionary branches of eukaryotes (Nosema locustae), Bacteria (Aquifex pyrophilus and Thermotoga maritima) and Archaea (Pyrococcus furiosus and Sulfolobus acidocaldarius). In addition, a new valyl-tRNA synthetase was characterized from the protist Trichomonas vaginalis. Different phylogenetic methods were used to generate trees of isoleucyl-tRNA synthetases rooted by valyl- and leucyl-tRNA synthetases. All isoleucyl-tRNA synthetase trees showed Archaea and Eucarya as sister groups, providing strong confirmation for the universal tree rooting reported by Iwabe et al. As well, there was strong support for the monophyly (sensu Hennig) of Archaea. The valyl-tRNA synthetase gene from Tr. vaginalis clustered with other eukaryotic ValRS genes, which may have been transferred from the mitochondrial genome to the nuclear genome, suggesting that this amitochondrial trichomonad once harbored an endosymbiotic bacterium.
基于单基因同源序列构建的通用树无法确定根节点。岩部等人[Iwabe, N., Kuma, K.-I., Hasegawa, M., Osawa, S. & Miyata, T. (1989) Proc. Natl. Acad. Sci. USA 86, 9355 - 9359]通过使用早于所有生物最后共同祖先的古老基因复制事件解决了这个问题。他们针对延伸因子和ATP酶亚基分别构建的、相互确定根节点的基因树显示,细菌(真细菌)首先从通用树中分支出来,古菌(古细菌)和真核生物(真核生物)为姐妹群。鉴于其对进化生物学的重要性以及对ATP酶数据集适用性的担忧,使用其他古老基因复制事件对通用树根节点进行评估至关重要。在本研究中,我们利用氨酰 - tRNA合成酶基因确定了通用树的根节点,氨酰 - tRNA合成酶基因是一个庞大的多基因家族,其分化可能早于原核生物和真核生物。从代表真核生物(蝗虫微孢子虫)、细菌(嗜热栖热菌和嗜热栖热放线菌)和古菌(激烈火球菌和嗜酸热硫化叶菌)深层进化分支的几个物种的异亮氨酰 - tRNA合成酶中,对一个约1600bp的保守区域进行了测序。此外,从原生生物阴道毛滴虫中鉴定出一种新的缬氨酰 - tRNA合成酶。使用不同的系统发育方法构建了以缬氨酰 - tRNA合成酶和亮氨酰 - tRNA合成酶为根节点的异亮氨酰 - tRNA合成酶树。所有异亮氨酰 - tRNA合成酶树都显示古菌和真核生物为姐妹群,有力地证实了岩部等人报道的通用树根节点情况。同样,也有力支持了古菌的单系性(根据亨尼希的定义)。阴道毛滴虫的缬氨酰 - tRNA合成酶基因与其他真核生物缬氨酰 - tRNA合成酶基因聚类,这些基因可能是从线粒体基因组转移到核基因组的,这表明这种无线粒体的滴虫曾经含有一种内共生细菌。