Djuika Carine F, Huerta-Cepas Jaime, Przyborski Jude M, Deil Sophia, Sanchez Cecilia P, Doerks Tobias, Bork Peer, Lanzer Michael, Deponte Marcel
Department of Parasitology, Ruprecht-Karls University, D-69120 Heidelberg, Germany.
Structural and Computational Biology Unit, European Molecular Biology Laboratory (EMBL), D-69117 Heidelberg, Germany.
Microb Cell. 2015 Jan 5;2(1):5-13. doi: 10.15698/mic2015.01.182.
Horizontal gene transfer has emerged as a crucial driving force for the evolution of eukaryotes. This also includes and related economically and clinically relevant apicomplexan parasites, whose rather small genomes have been shaped not only by natural selection in different host populations but also by horizontal gene transfer following endosymbiosis. However, there is rather little reliable data on horizontal gene transfer between animal hosts or bacteria and apicomplexan parasites. Here we show that apicomplexan homologues of peroxiredoxin 5 (Prx5) have a prokaryotic ancestry and therefore represent a special subclass of Prx5 isoforms in eukaryotes. Using two different immunobiochemical approaches, we found that the Prx5 homologue is dually localized to the parasite plastid and cytosol. This dual localization is reflected by a modular -specific gene architecture consisting of two exons. Despite the plastid localization, our phylogenetic analyses contradict an acquisition by secondary endosymbiosis and support a gene fusion event following a horizontal prokaryote-to-eukaryote gene transfer in early apicomplexans. The results provide unexpected insights into the evolution of apicomplexan parasites as well as the molecular evolution of peroxiredoxins, an important family of ubiquitous, usually highly concentrated thiol-dependent hydroperoxidases that exert functions as detoxifying enzymes, redox sensors and chaperones.
水平基因转移已成为真核生物进化的关键驱动力。这也包括与经济和临床相关的顶复门寄生虫,其相对较小的基因组不仅受到不同宿主群体中自然选择的影响,还受到内共生后水平基因转移的影响。然而,关于动物宿主或细菌与顶复门寄生虫之间水平基因转移的可靠数据相当少。在这里,我们表明过氧化物还原酶5(Prx5)的顶复门同源物具有原核生物起源,因此代表了真核生物中Prx5亚型的一个特殊亚类。使用两种不同的免疫生化方法,我们发现Prx5同源物双重定位于寄生虫的质体和细胞质中。这种双重定位由一个由两个外显子组成的模块化基因结构所反映。尽管定位于质体,但我们的系统发育分析与通过二次内共生获得的情况相矛盾,并支持在早期顶复门生物中发生的从原核生物到真核生物的水平基因转移后的基因融合事件。这些结果为顶复门寄生虫的进化以及过氧化物还原酶的分子进化提供了意想不到的见解,过氧化物还原酶是一类重要的普遍存在的、通常高度浓缩的硫醇依赖性氢过氧化物酶,具有解毒酶、氧化还原传感器和伴侣的功能。