Michel Mickael, Marzena Łazarczyk, Norwin Kubick, Agata Gurba, Tomasz Kocki, Jarosław Olav Horbańczuk, Atanas G Atanasov, Mariusz Sacharczuk, Piotr Religa
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To shed light on these mysteries, we conducted a comprehensive evolutionary analysis employing a range of tools, including multiple sequence alignment, phylogenetic tree construction, ancestral sequence reconstruction, and positive selection assessment. Our investigations revealed intriguing insights. AIRE1 homologs emerged during the divergence of T cells in higher vertebrates, signifying its role in this context. Conversely, FEZF2 exhibited multiple homologs spanning invertebrates, lampreys, and higher vertebrates. Ancestral sequence reconstruction demonstrated distinct origins for AIRE1 and FEZF2, underscoring that their roles in regulating TRA have evolved through disparate pathways. Furthermore, it became evident that both FEZF2 and AIRE1 govern a diverse repertoire of genes, encompassing ancient and more recently diverged targets. Notably, FEZF2 demonstrates expression in both vertebrate and invertebrate embryos and germlines, accentuating its widespread role. Intriguingly, FEZF2 harbors motifs associated with autophagy, such as DKFPHP, SYSELWKSSL, and SYSEL, a process integral to cell selection in invertebrates. Our findings suggest that FEZF2 initially emerged to regulate self-elimination in the gonads of invertebrates. As organisms evolved toward greater complexity, AIRE1 likely emerged to complement FEZF2's role, participating in the regulation of cell selection for elimination in both gonads and the thymus. 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引用次数: 0
摘要
自身免疫调节因子 1(AIRE1)和前脑胚胎锌指样蛋白 2(FEZF2)在协调组织限制性抗原(TRA)的表达以促进自身反应性 T 细胞的消除方面发挥着关键作用。AIRE1 存在于各种脊椎动物的性腺中,这引起了人们对其可能参与生殖细胞选择的基因表达控制的质疑。然而,这些基因的进化史仍然是个谜,它们在脊椎动物中明显冗余的原因也是如此。此外,淘汰过程本身的起源也一直难以捉摸。为了揭开这些谜团,我们利用一系列工具进行了全面的进化分析,包括多序列比对、系统发生树构建、祖先序列重建和正选择评估。我们的研究揭示了耐人寻味的见解。在高等脊椎动物的T细胞分化过程中出现了AIRE1同源物,这表明AIRE1在这一过程中扮演着重要角色。相反,FEZF2在无脊椎动物、灯鱼和高等脊椎动物中出现了多个同源物。祖先序列重建表明,AIRE1 和 FEZF2 的起源不同,这突出表明它们在调节 TRA 中的作用是通过不同的途径进化而来的。此外,FEZF2和AIRE1显然都调控着不同的基因,包括古老的和新近分化的目标基因。值得注意的是,FEZF2 在脊椎动物和无脊椎动物的胚胎和生殖系中都有表达,这突出了它的广泛作用。耐人寻味的是,FEZF2含有与自噬相关的基序,如DKFPHP、SYSELWKSSL和SYSEL,而自噬是无脊椎动物细胞选择不可或缺的过程。我们的研究结果表明,FEZF2的出现最初是为了调节无脊椎动物性腺中的自噬。随着生物向更复杂的方向进化,AIRE1的出现很可能是对FEZF2作用的补充,它参与了性腺和胸腺中细胞选择淘汰的调控。AIRE1和FEZF2之间的这种动态相互作用凸显了它们在不同进化背景下对TRA表达调控的多方面贡献。
FEZF2 and AIRE1: An Evolutionary Trade-off in the Elimination of Auto-reactive T Cells in the Thymus.
Autoimmune Regulator 1 (AIRE1) and Forebrain Embryonic Zinc Finger-Like Protein 2 (FEZF2) play pivotal roles in orchestrating the expression of tissue-restricted antigens (TRA) to facilitate the elimination of autoreactive T cells. AIRE1's presence in the gonads of various vertebrates has raised questions about its potential involvement in gene expression control for germline cell selection. Nevertheless, the evolutionary history of these genes has remained enigmatic, as has the rationale behind their apparent redundancy in vertebrates. Furthermore, the origin of the elimination process itself has remained elusive. To shed light on these mysteries, we conducted a comprehensive evolutionary analysis employing a range of tools, including multiple sequence alignment, phylogenetic tree construction, ancestral sequence reconstruction, and positive selection assessment. Our investigations revealed intriguing insights. AIRE1 homologs emerged during the divergence of T cells in higher vertebrates, signifying its role in this context. Conversely, FEZF2 exhibited multiple homologs spanning invertebrates, lampreys, and higher vertebrates. Ancestral sequence reconstruction demonstrated distinct origins for AIRE1 and FEZF2, underscoring that their roles in regulating TRA have evolved through disparate pathways. Furthermore, it became evident that both FEZF2 and AIRE1 govern a diverse repertoire of genes, encompassing ancient and more recently diverged targets. Notably, FEZF2 demonstrates expression in both vertebrate and invertebrate embryos and germlines, accentuating its widespread role. Intriguingly, FEZF2 harbors motifs associated with autophagy, such as DKFPHP, SYSELWKSSL, and SYSEL, a process integral to cell selection in invertebrates. Our findings suggest that FEZF2 initially emerged to regulate self-elimination in the gonads of invertebrates. As organisms evolved toward greater complexity, AIRE1 likely emerged to complement FEZF2's role, participating in the regulation of cell selection for elimination in both gonads and the thymus. This dynamic interplay between AIRE1 and FEZF2 underscores their multifaceted contributions to TRA expression regulation across diverse evolutionary contexts.
期刊介绍:
Journal of Molecular Evolution covers experimental, computational, and theoretical work aimed at deciphering features of molecular evolution and the processes bearing on these features, from the initial formation of macromolecular systems through their evolution at the molecular level, the co-evolution of their functions in cellular and organismal systems, and their influence on organismal adaptation, speciation, and ecology. Topics addressed include the evolution of informational macromolecules and their relation to more complex levels of biological organization, including populations and taxa, as well as the molecular basis for the evolution of ecological interactions of species and the use of molecular data to infer fundamental processes in evolutionary ecology. This coverage accommodates such subfields as new genome sequences, comparative structural and functional genomics, population genetics, the molecular evolution of development, the evolution of gene regulation and gene interaction networks, and in vitro evolution of DNA and RNA, molecular evolutionary ecology, and the development of methods and theory that enable molecular evolutionary inference, including but not limited to, phylogenetic methods.