論文

査読有り 国際誌
2020年3月9日

Highly Reduced Genomes of Protist Endosymbionts Show Evolutionary Convergence.

Current biology : CB
  • Emma E George
  • ,
  • Filip Husnik
  • ,
  • Daria Tashyreva
  • ,
  • Galina Prokopchuk
  • ,
  • Aleš Horák
  • ,
  • Waldan K Kwong
  • ,
  • Julius Lukeš
  • ,
  • Patrick J Keeling

30
5
開始ページ
925
終了ページ
933
記述言語
英語
掲載種別
DOI
10.1016/j.cub.2019.12.070

Genome evolution in bacterial endosymbionts is notoriously extreme: the combined effects of strong genetic drift and unique selective pressures result in highly reduced genomes with distinctive adaptations to hosts [1-4]. These processes are mostly known from animal endosymbionts, where nutritional endosymbioses represent the best-studied systems. However, eukaryotic microbes, or protists, also harbor diverse bacterial endosymbionts, but their genome reduction and functional relationships with their hosts are largely unexplored [5-7]. We sequenced the genomes of four bacterial endosymbionts from three species of diplonemids, poorly studied but abundant and diverse heterotrophic protists [8-12]. The endosymbionts come from two bacterial families, Rickettsiaceae and Holosporaceae, that have invaded two families of diplonemids, and their genomes have converged on an extremely small size (605-632 kilobase pairs [kbp]), similar gene content (e.g., metabolite transporters and secretion systems), and reduced metabolic potential (e.g., loss of energy metabolism). These characteristics are generally found in both families, but the diplonemid endosymbionts have evolved greater extremes in parallel. They possess modified type VI secretion systems that could function in manipulating host metabolism or other intracellular interactions. Finally, modified cellular machinery like the ATP synthase without oxidative phosphorylation, and the reduced flagellar apparatus present in some diplonemid endosymbionts and nutritional animal endosymbionts, indicates that intracellular mechanisms have converged in bacterial endosymbionts with various functions and from different eukaryotic hosts across the tree of life.

リンク情報
DOI
https://doi.org/10.1016/j.cub.2019.12.070
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31978335

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