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基因与基因组的物种形成:错配修复系统引发的重组障碍对DNA多态性的保守作用

Speciation of Genes and Genomes: Conservation of DNA Polymorphism by Barriers to Recombination Raised by Mismatch Repair System.

作者信息

Radman Miroslav

机构信息

Mediterranean Institute for Life Sciences-MedILS, Split, Croatia.

Faculty of Medicine, University R. Descartes, Paris, France.

出版信息

Front Genet. 2022 Feb 28;13:803690. doi: 10.3389/fgene.2022.803690. eCollection 2022.

Abstract

Some basic aspects of human and animal biology and evolution involve the establishment of biological uniqueness of species and individuals within their huge variety. The discrimination among closely related species occurs in their offspring at the level of chromosomal DNA sequence homology, which is required for fertility as the hallmark of species. Biological identification of individuals, i.e., of their biological "self", occurs at the level of protein sequences presented by the MHC/HLA complex as part of the immune system that discriminates non-self from self. Here, a mechanistic molecular model is presented that can explain how DNA sequence divergence and the activity of key mismatch repair proteins, MutS and MutL, lead to 1) genetic separation of closely related species (sympatric speciation) (Fitch and Ayala, Proceedings of the National Academy of Sciences, 1994, 91, 6717-6720), 2) the stability of genomes riddled by diverged repeated sequences, and 3) conservation of highly polymorphic DNA sequence blocks that constitute the immunological self. All three phenomena involve suppression of recombination between diverged homologies, resulting in prevention of gene sharing between closely related genomes (evolution of new species) as well as sequence sharing between closely related genes within a genome (e.g., evolution of immunoglobulin, MHC, and other gene families bearing conserved polymorphisms).

摘要

人类和动物生物学及进化的一些基本方面涉及在种类繁多的物种和个体中确立其生物学独特性。在亲缘关系密切的物种之间,其后代在染色体DNA序列同源性水平上存在差异,而这种同源性是作为物种标志的生育能力所必需的。个体的生物学识别,即对其生物学“自我”的识别,发生在作为免疫系统一部分的MHC/HLA复合体所呈现的蛋白质序列水平上,该系统能区分自我与非自我。在此,我们提出一个机制性分子模型,它可以解释DNA序列差异以及关键错配修复蛋白MutS和MutL的活性如何导致:1)亲缘关系密切的物种的遗传分离(同域物种形成)(菲奇和阿亚拉,《美国国家科学院院刊》,1994年,91卷,6717 - 6720页),2)充满差异重复序列的基因组的稳定性,以及3)构成免疫自我的高度多态性DNA序列块的保守性。这三种现象都涉及抑制差异同源序列之间的重组,从而防止亲缘关系密切的基因组之间的基因共享(新物种的进化)以及基因组内亲缘关系密切的基因之间的序列共享(例如,免疫球蛋白、MHC和其他具有保守多态性的基因家族的进化)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35ae/8918686/85ab46920a84/fgene-13-803690-g001.jpg

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