Conservation of antiviral systems across domains of life reveals immune genes in humans

IF 20.6 1区 医学 Q1 MICROBIOLOGY
Jean Cury, Matthieu Haudiquet, Veronica Hernandez Trejo, Ernest Mordret, Anael Hanouna, Maxime Rotival, Florian Tesson, Delphine Bonhomme, Gal Ofir, Lluis Quintana-Murci, Philippe Benaroch, Enzo Z. Poirier, Aude Bernheim
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Abstract

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.

Abstract Image

跨生命领域的抗病毒系统保护揭示了人类的免疫基因
破译真核生物的免疫组织对于人类健康和了解生态系统非常重要。最近发现的抗虹吸系统揭示了各种真核生物免疫蛋白源自原核生物抗虹吸系统。然而,细菌的抗虹吸蛋白是否能揭示真核生物的免疫组织仍有待探索。在这里,我们利用系统发育驱动的方法,通过寻找细菌抗虹吸系统的同源物来发现真核生物的免疫蛋白。我们证明,与最近发现的抗虹吸系统具有序列相似性的蛋白质广泛存在于真核生物中,并在人类免疫中发挥作用。抗转座子 piRNA 途径中的两个真核生物蛋白在进化上与抗虹吸系统 Mokosh 有关。此外,人类免疫相关蛋白 GTPases(GIMAPs)以及微合成中编码的两个基因 FHAD1 和 CTRC 分别与 Eleos 和 Lamassu 原核系统有关,并表现出抗病毒活性。我们的工作说明了免疫机制比较基因组学如何发现真核生物的防御基因。
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来源期刊
Cell host & microbe
Cell host & microbe 生物-微生物学
CiteScore
45.10
自引率
1.70%
发文量
201
审稿时长
4-8 weeks
期刊介绍: Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.
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