Kamikawa Ryoma, Inagaki Yuji, Sako Yoshihiko
Laboratory of Marine Microbiology, Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.
Proc Natl Acad Sci U S A. 2008 May 13;105(19):6965-9. doi: 10.1073/pnas.0711084105. Epub 2008 May 5.
Genes encoding elongation factor-like (EFL) proteins, which show high similarity to elongation factor-1alpha (EF-1alpha), have been found in phylogenetically distantly related eukaryotes. The sporadic distribution of "EFL-containing" lineages within "EF-1alpha-containing" lineages indirectly, but strongly, suggests lateral gene transfer as the principal driving force in EFL evolution. However, one of the most critical aspects in the above hypothesis, the donor lineages in any putative cases of lateral EFL gene transfer, remained unclear. In this study, we provide direct evidence for lateral transfer of an EFL gene through the analyses of 10 diatom EFL genes. All diatom EFL homologues tightly clustered in phylogenetic analyses, suggesting acquisition of the exogenous EFL gene early in diatom evolution. Our survey additionally identified Thalassiosira pseudonana as a eukaryote bearing EF-1alpha and EFL genes and secondary EFL gene loss in Phaeodactylum tricornutum, the complete genome of which encodes only the EF-1alpha gene. Most importantly, the EFL phylogeny recovered a robust grouping of homologues from diatoms, the cercozoan Bigelowiella natans, and the foraminifer Planoglabratella opecularis, with the diatoms nested within the Bigelowiella plus Planoglabratella (Rhizaria) grouping. The particular relationships recovered are further consistent with two characteristic sequence motifs. The best explanation of our data analyses is an EFL gene transfer from a foraminifer to a diatom, the first case in which the donor-recipient relationship was clarified. Finally, based on a reverse transcriptase quantitative PCR assay and the genome information of Thalassiosira and Phaeodactylum, we propose the loss of elongation factor function in Thalassiosira EF-1alpha.
编码与延伸因子-1α(EF-1α)高度相似的延伸因子样(EFL)蛋白的基因,已在系统发育关系较远的真核生物中被发现。“含EFL”谱系在“含EF-1α”谱系中的零星分布间接但有力地表明,横向基因转移是EFL进化的主要驱动力。然而,上述假说中最关键的一个方面,即在任何假定的EFL基因横向转移案例中的供体谱系,仍不清楚。在本研究中,我们通过对10个硅藻EFL基因的分析,为EFL基因的横向转移提供了直接证据。在系统发育分析中,所有硅藻EFL同源物紧密聚类,表明在硅藻进化早期获得了外源EFL基因。我们的调查还鉴定出拟菱形藻是一种同时携带EF-1α和EFL基因的真核生物,而三角褐指藻存在EFL基因的二次丢失,其完整基因组仅编码EF-1α基因。最重要的是,EFL系统发育分析恢复了一个强大的同源物分组,包括来自硅藻、cercozoan的比氏硅藻和有孔虫的透明有孔虫,其中硅藻嵌套在比氏硅藻加透明有孔虫(根足亚纲)分组中。所恢复的特定关系进一步与两个特征性序列基序一致。我们数据分析的最佳解释是EFL基因从有孔虫转移到硅藻,这是首次明确供体-受体关系的案例。最后,基于逆转录酶定量PCR分析以及硅藻和三角褐指藻的基因组信息,我们提出硅藻EF-1α中延伸因子功能的丧失。