Nývltová Eva, Stairs Courtney W, Hrdý Ivan, Rídl Jakub, Mach Jan, Pačes Jan, Roger Andrew J, Tachezy Jan
Department of Parasitology, Faculty of Science, Charles University in Prague, Viničná, Prague, Czech Republic.
Centre for Comparative Genomics and Evolutionary Bioinformatics, Dalhousie University, Halifax, NS, Canada.
Mol Biol Evol. 2015 Apr;32(4):1039-55. doi: 10.1093/molbev/msu408. Epub 2015 Jan 7.
Lateral gene transfer (LGT) is an important mechanism of evolution for protists adapting to oxygen-poor environments. Specifically, modifications of energy metabolism in anaerobic forms of mitochondria (e.g., hydrogenosomes) are likely to have been associated with gene transfer from prokaryotes. An interesting question is whether the products of transferred genes were directly targeted into the ancestral organelle or initially operated in the cytosol and subsequently acquired organelle-targeting sequences. Here, we identified key enzymes of hydrogenosomal metabolism in the free-living anaerobic amoebozoan Mastigamoeba balamuthi and analyzed their cellular localizations, enzymatic activities, and evolutionary histories. Additionally, we characterized 1) several canonical mitochondrial components including respiratory complex II and the glycine cleavage system, 2) enzymes associated with anaerobic energy metabolism, including an unusual D-lactate dehydrogenase and acetyl CoA synthase, and 3) a sulfate activation pathway. Intriguingly, components of anaerobic energy metabolism are present in at least two gene copies. For each component, one copy possesses an mitochondrial targeting sequence (MTS), whereas the other lacks an MTS, yielding parallel cytosolic and hydrogenosomal extended glycolysis pathways. Experimentally, we confirmed that the organelle targeting of several proteins is fully dependent on the MTS. Phylogenetic analysis of all extended glycolysis components suggested that these components were acquired by LGT. We propose that the transformation from an ancestral organelle to a hydrogenosome in the M. balamuthi lineage involved the lateral acquisition of genes encoding extended glycolysis enzymes that initially operated in the cytosol and that established a parallel hydrogenosomal pathway after gene duplication and MTS acquisition.
横向基因转移(LGT)是原生生物适应缺氧环境的一种重要进化机制。具体而言,厌氧形式的线粒体(如氢化酶体)中能量代谢的改变很可能与来自原核生物的基因转移有关。一个有趣的问题是,转移基因的产物是直接靶向到祖先细胞器中,还是最初在细胞质中发挥作用,随后获得细胞器靶向序列。在这里,我们鉴定了自由生活的厌氧变形虫巴氏鞭毛虫(Mastigamoeba balamuthi)中氢化酶体代谢的关键酶,并分析了它们的细胞定位、酶活性和进化历史。此外,我们还对以下几类物质进行了表征:1)几种典型的线粒体成分,包括呼吸复合体II和甘氨酸裂解系统;2)与厌氧能量代谢相关的酶,包括一种不寻常的D - 乳酸脱氢酶和乙酰辅酶A合成酶;3)一条硫酸盐激活途径。有趣的是,厌氧能量代谢的成分至少存在两个基因拷贝。对于每个成分,一个拷贝拥有线粒体靶向序列(MTS),而另一个则缺乏MTS,从而产生平行的细胞质和氢化酶体延伸糖酵解途径。通过实验,我们证实了几种蛋白质的细胞器靶向完全依赖于MTS。对所有延伸糖酵解成分的系统发育分析表明,这些成分是通过LGT获得的。我们提出,巴氏鞭毛虫谱系中从祖先细胞器到氢化酶体的转变涉及横向获取编码延伸糖酵解酶的基因,这些基因最初在细胞质中发挥作用,并在基因复制和获得MTS后建立了平行的氢化酶体途径。