Research Center in Biodiversity and Genetic Resources (CIBIO-InBIO), University of Porto, Vairão, Portugal.
Max von Pettenkofer Institute and Gene Center, Virology, National Reference Center for Retroviruses, Faculty of Medicine, Ludwig Maximilian University of Munich (LMU) München, Munich, Germany.
Front Immunol. 2022 Feb 9;13:752186. doi: 10.3389/fimmu.2022.752186. eCollection 2022.
Guanylate binding proteins (GBPs) are paramount in the host immunity by providing defense against invading pathogens. Multigene families related to the immune system usually show that the duplicated genes can either undergo deletion, gain new functions, or become non-functional. Here, we show that in muroids, the genes followed an unusual pattern of gain and loss of genes. Muroids present a high diversity and plasticity regarding synteny, with most species presenting two gene clusters. The phylogenetic analyses revealed seven different groups. Three of them clustered with , and of primates. Four new genes that appear to be exclusive to muroids were identified as , , and . A duplication event occurred in the group in the common ancestor of Muridae and Cricetidae (~20 Mya), but both copies were deleted from the genome of , and . The gene emerged in the ancestor of Muridae and Cricetidae and evolved independently originating in Muridae, and in Cricetidae. Since appears only in three species, we hypothesize that it was present in the common ancestor and deleted from most muroid genomes. The second gene cluster, , is widespread across all muroids, indicating that this cluster emerged before the Muridae and Cricetidae radiation. An expansion of occurred in and probably to compensate the loss of and . is divided in three groups and is present in most muroids suggesting that a duplication event occurred in the common ancestor of Muridae and Cricetidae. However, in and is absent, and in appears to have been deleted. Our results further demonstrated that primate , and are absent from the genome of muroids and showed that the gene annotations in muroids were incorrect. We propose a new classification based on the phylogenetic analyses and the divergence between the groups. Extrapolations to humans based on functional studies of muroid should be re-evaluated. The evolutionary analyses of muroid genes provided new insights about the evolution and function of these genes.
鸟苷酸结合蛋白(GBP)在宿主免疫中起着至关重要的作用,为抵御入侵病原体提供了防御。与免疫系统相关的多基因家族通常表明,复制基因要么经历缺失,获得新功能,要么失去功能。在这里,我们表明在啮齿动物中,基因经历了基因获得和丢失的不寻常模式。啮齿动物在基因排列上表现出高度的多样性和可塑性,大多数物种都有两个基因簇。系统发育分析显示出七个不同的基因簇。其中三个与灵长类动物的、和聚类。鉴定出四个新的似乎仅存在于啮齿动物中的基因,分别为、和。在鼠科和仓鼠科的共同祖先中发生了一次在 基因簇中的复制事件(~20 Mya),但这两个拷贝都从的基因组中删除了,和。基因出现在鼠科和仓鼠科的祖先中,并独立进化,起源于鼠科,和起源于仓鼠科。由于只出现在三个物种中,我们假设它存在于共同祖先中,并从大多数啮齿动物的基因组中删除。第二个基因簇,出现在所有的啮齿动物中,表明这个基因簇在鼠科和仓鼠科辐射之前就已经出现。发生了扩张,可能是为了补偿和的缺失。基因分为三组,存在于大多数啮齿动物中,这表明在鼠科和仓鼠科的共同祖先中发生了复制事件。然而,在和中缺失,而在中似乎被删除。我们的研究结果进一步表明,灵长类动物的、和在啮齿动物的基因组中缺失,并表明啮齿动物中基因的注释是不正确的。我们提出了一种基于系统发育分析和群体间分化的新分类。基于对啮齿动物基因的功能研究的人类推断应该重新评估。对啮齿动物基因的进化分析提供了这些基因进化和功能的新见解。