Evolutionary Biology Group, Faculty of Biology, Adam Mickiewicz University, Poznan, Poland.
Institute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Krakow, Poland.
Trends Genet. 2020 Apr;36(4):298-311. doi: 10.1016/j.tig.2020.01.008. Epub 2020 Feb 7.
Proteins encoded by the classical major histocompatibility complex (MHC) genes incite the vertebrate adaptive immune response by presenting peptide antigens on the cell surface. Here, we review mechanisms explaining landmark features of these genes: extreme polymorphism, excess of nonsynonymous changes in peptide-binding domains, and long gene genealogies. Recent studies provide evidence that these features may arise due to pathogens evolving ways to evade immune response guided by the locally common MHC alleles. However, complexities of selection on MHC genes are simultaneously being revealed that need to be incorporated into existing theory. These include pathogen-driven selection for antigen-binding breadth and expansion of the MHC gene family, associated autoimmunity trade-offs, hitchhiking of deleterious mutations linked to the MHC, geographic subdivision, and adaptive introgression.
经典主要组织相容性复合体 (MHC) 基因编码的蛋白质通过在细胞表面呈现肽抗原来引发脊椎动物适应性免疫反应。在这里,我们回顾了解释这些基因标志性特征的机制:极端多态性、肽结合域中非同义突变的过剩以及长基因谱系。最近的研究提供了证据表明,这些特征可能是由于病原体进化出了逃避由局部常见 MHC 等位基因指导的免疫反应的方法而产生的。然而,MHC 基因选择的复杂性同时也在被揭示出来,需要将其纳入现有理论中。这些复杂性包括病原体驱动的抗原结合广度选择和 MHC 基因家族的扩张,与 MHC 相关的自身免疫权衡,与 MHC 相关的有害突变的搭便车,地理细分以及适应性渗入。