Molecular Diversity of Microbes, Institut Pasteur, CNRS UMR3525, INSERM U1284, Université Paris-Cité, 75015 Paris, France.
Molecular Diversity of Microbes, Institut Pasteur, CNRS UMR3525, INSERM U1284, Université Paris-Cité, 75015 Paris, France; Innate Immunity in Physiology and Cancer Team, Institut Curie, PSL Research University, INSERM U932, 75005 Paris, France.
Cell Host Microbe. 2024 Sep 11;32(9):1594-1607.e5. doi: 10.1016/j.chom.2024.08.002. Epub 2024 Aug 28.
Deciphering the immune organization of eukaryotes is important for human health and for understanding ecosystems. The recent discovery of antiphage systems revealed that various eukaryotic immune proteins originate from prokaryotic antiphage systems. However, whether bacterial antiphage proteins can illuminate immune organization in eukaryotes remains unexplored. Here, we use a phylogeny-driven approach to uncover eukaryotic immune proteins by searching for homologs of bacterial antiphage systems. We demonstrate that proteins displaying sequence similarity with recently discovered antiphage systems are widespread in eukaryotes and maintain a role in human immunity. Two eukaryotic proteins of the anti-transposon piRNA pathway are evolutionarily linked to the antiphage system Mokosh. Additionally, human GTPases of immunity-associated proteins (GIMAPs) as well as two genes encoded in microsynteny, FHAD1 and CTRC, are respectively related to the Eleos and Lamassu prokaryotic systems and exhibit antiviral activity. Our work illustrates how comparative genomics of immune mechanisms can uncover defense genes in eukaryotes.
解析真核生物的免疫组织对于人类健康和理解生态系统都很重要。最近发现的抗噬菌体系统表明,各种真核免疫蛋白源自原核抗噬菌体系统。然而,细菌抗噬菌体蛋白是否能阐明真核生物的免疫组织仍未得到探索。在这里,我们使用一种基于系统发育的方法,通过搜索细菌抗噬菌体系统的同源物来发现真核生物的免疫蛋白。我们证明,与最近发现的抗噬菌体系统具有序列相似性的蛋白在真核生物中广泛存在,并在人类免疫中发挥作用。反转座子 piRNA 途径的两种真核蛋白与抗噬菌体系统 Mokosh 在进化上有关联。此外,人类免疫相关蛋白(GIMAPs)中的 GTPases 以及微同线性编码的两个基因 FHAD1 和 CTRC,分别与 Eleos 和 Lamassu 原核系统有关,并表现出抗病毒活性。我们的工作说明了比较基因组学免疫机制如何能揭示真核生物的防御基因。