Santana-Molina Carlos, Williams Tom A, Snel Berend, Spang Anja
Department of Marine Microbiology and Biogeochemistry, NIOZ, Royal Netherlands Institute for Sea Research, AB Den Burg, the Netherlands.
Bristol Palaeobiology Group, School of Biological Sciences, University of Bristol, Bristol, UK.
Nat Ecol Evol. 2025 Apr;9(4):613-627. doi: 10.1038/s41559-025-02648-0. Epub 2025 Mar 3.
The origin of eukaryotes was a key event in the history of life. Current leading hypotheses propose that a symbiosis between an asgardarchaeal host cell and an alphaproteobacterial endosymbiont represented a crucial step in eukaryotic origin and that metabolic cross-feeding between the partners provided the basis for their subsequent evolutionary integration. A major unanswered question is whether the metabolism of modern eukaryotes bears any vestige of this ancestral syntrophy. Here we systematically analyse the evolutionary origins of the eukaryotic gene repertoires mediating central carbon metabolism. Our phylogenetic and sequence analyses reveal that this gene repertoire is chimeric, with ancestral contributions from Asgardarchaeota and Alphaproteobacteria operating predominantly in glycolysis and the tricarboxylic acid cycle, respectively. Our analyses also reveal the extent to which this ancestral metabolic interplay has been remodelled via gene loss, transfer and subcellular retargeting in the >2 billion years since the origin of eukaryotic cells, and we identify genetic contributions from other prokaryotic sources in addition to the asgardarchaeal host and alphaproteobacterial endosymbiont. Our work demonstrates that, in contrast to previous assumptions, modern eukaryotic metabolism preserves information about the nature of the original asgardarchaeal-alphaproteobacterial interactions and supports syntrophy scenarios for the origin of the eukaryotic cell.
真核生物的起源是生命史上的一个关键事件。当前主流假说认为,阿斯加德古菌宿主细胞与α-变形菌内共生体之间的共生关系是真核生物起源的关键一步,且共生伙伴之间的代谢交叉喂养为它们随后的进化整合提供了基础。一个主要未解决的问题是现代真核生物的代谢是否保留了这种原始互养的任何痕迹。在这里,我们系统地分析了介导中心碳代谢的真核基因库的进化起源。我们的系统发育和序列分析表明,这个基因库是嵌合的,阿斯加德古菌和α-变形菌的祖先贡献分别主要作用于糖酵解和三羧酸循环。我们的分析还揭示了自真核细胞起源以来的20多亿年里,这种原始代谢相互作用通过基因丢失、转移和亚细胞重新定位被重塑的程度,并且我们确定了除阿斯加德古菌宿主和α-变形菌内共生体外其他原核生物来源的遗传贡献。我们的研究表明,与之前的假设相反,现代真核生物代谢保留了有关原始阿斯加德古菌- α-变形菌相互作用性质的信息,并支持真核细胞起源的互养假说。