Simpson Alastair G B, Inagaki Yuji, Roger Andrew J
Canadian Institute for Advanced Research, Program in Evolutionary Biology, Dalhousie University, Halifax, Nova Scotia, Canada.
Mol Biol Evol. 2006 Mar;23(3):615-25. doi: 10.1093/molbev/msj068. Epub 2005 Nov 24.
Many of the protists thought to represent the deepest branches on the eukaryotic tree are assigned to a loose assemblage called the "excavates." This includes the mitochondrion-lacking diplomonads and parabasalids (e.g., Giardia and Trichomonas) and the jakobids (e.g., Reclinomonas). We report the first multigene phylogenetic analyses to include a comprehensive sampling of excavate groups (six nuclear-encoded protein-coding genes, nine of the 10 recognized excavate groups). Excavates coalesce into three clades with relatively strong maximum likelihood bootstrap support. Only the phylogenetic position of Malawimonas is uncertain. Diplomonads, parabasalids, and the free-living amitochondriate protist Carpediemonas are closely related to each other. Two other amitochondriate excavates, oxymonads and Trimastix, form the second monophyletic group. The third group is comprised of Euglenozoa (e.g., trypanosomes), Heterolobosea, and jakobids. Unexpectedly, jakobids appear to be specifically related to Heterolobosea. This tree topology calls into question the concept of Discicristata as a supergroup of eukaryotes united by discoidal mitochondrial cristae and makes it implausible that jakobids represent an independent early-diverging eukaryotic lineage. The close jakobids-Heterolobosea-Euglenozoa connection demands complex evolutionary scenarios to explain the transition between the presumed ancestral bacterial-type mitochondrial RNA polymerase found in jakobids and the phage-type protein in other eukaryotic lineages, including Euglenozoa and Heterolobosea.
许多被认为代表真核生物树最深分支的原生生物被归入一个名为“挖掘类”的松散类群。这包括缺乏线粒体的双滴虫和副基体(如贾第虫和毛滴虫)以及贾科比虫(如 reclinomonas)。我们报告了首次多基因系统发育分析,其中包括对挖掘类群的全面抽样(六个核编码蛋白质编码基因,10 个公认挖掘类群中的 9 个)。挖掘类聚为三个分支,具有相对较强的最大似然自展支持。只有马拉维单胞菌的系统发育位置不确定。双滴虫、副基体和自由生活的无线粒体原生生物卡氏鞭毛虫彼此密切相关。另外两种无线粒体挖掘类生物,即微滴虫和三鞭毛虫,形成了第二个单系群。第三个类群由眼虫动物门(如锥虫)、异叶足虫纲和贾科比虫组成。出乎意料的是,贾科比虫似乎与异叶足虫纲有特定的亲缘关系。这种树拓扑结构对盘状嵴真核生物作为一个由盘状线粒体嵴联合的真核生物超群的概念提出了质疑,并使得贾科比虫代表一个独立的早期分化真核生物谱系变得不合理。贾科比虫 - 异叶足虫纲 - 眼虫动物门的紧密联系需要复杂的进化场景来解释在贾科比虫中发现的假定祖先细菌型线粒体 RNA 聚合酶与其他真核生物谱系(包括眼虫动物门和异叶足虫纲)中的噬菌体型蛋白质之间的转变。