Carlyle James R, Mesci Aruz, Fine Jason H, Chen Peter, Bélanger Simon, Tai Lee-Hwa, Makrigiannis Andrew P
Department of Immunology, University of Toronto & Sunnybrook Research Institute, 2075 Bayview Avenue (S-236), Toronto, ON M4N 3M5, Canada.
Semin Immunol. 2008 Dec;20(6):321-30. doi: 10.1016/j.smim.2008.05.004. Epub 2008 Jul 2.
The Ly49 and Nkrp1 loci encode structurally and functionally related cell surface proteins that positively or negatively regulate natural killer (NK) cell-mediated cytotoxicity and cytokine production. Yet despite their clear relatedness and genetic linkage within the NK gene complex (NKC), these two multi-gene families have adopted dissimilar evolutionary strategies. The Ly49 genes are extremely polymorphic and evolutionarily dynamic, with distinct gene numbers, remarkable allelic diversity, and varying MHC-I-ligand specificities and affinities among different murine haplotypes. In contrast, the Nkrp1 genes have opted for overall conservation of genomic organization, sequences, and ligand specificities, with only limited and focused allelic polymorphism. Possible selection pressures driving such varied evolution of the two gene families may include disequilibrium from ligand co-inheritance, pathogen immunoevasin strategies, flexibility in host counter-evolution mechanisms, and the prevalence and dynamics of inherent repetitive elements.
Ly49和Nkrp1基因座编码结构和功能相关的细胞表面蛋白,这些蛋白可正向或负向调节自然杀伤(NK)细胞介导的细胞毒性和细胞因子产生。然而,尽管它们在NK基因复合体(NKC)中具有明显的相关性和遗传连锁性,但这两个多基因家族却采用了不同的进化策略。Ly49基因具有极高的多态性且在进化上动态变化,不同小鼠单倍型之间的基因数量不同、等位基因多样性显著,且MHC-I配体特异性和亲和力各异。相比之下,Nkrp1基因选择了基因组组织、序列和配体特异性的整体保守,仅存在有限且集中的等位基因多态性。驱动这两个基因家族如此多样化进化的可能选择压力包括配体共同遗传的不平衡、病原体免疫逃避策略、宿主反进化机制的灵活性以及固有重复元件的流行和动态变化。