College of Ecology and Nature Conservation, Beijing Forestry University, Beijing 100085, China.
Institute of Wetland Research, Chinese Academy of Forestry, Beijing Key Laboratory of Wetland Services and Restoration, Beijing 100091, China.
Genes (Basel). 2022 May 23;13(5):928. doi: 10.3390/genes13050928.
Major histocompatibility complex (MHC) genes are the most polymorphic in vertebrates and the high variability in many MHC genes is thought to play a crucial role in pathogen recognition. The MHC class II locus DQA polymorphism was analyzed in the endangered Przewalski's horse, , a species that has been extinct in the wild and all the current living individuals descend from 12 founders. We used the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) to detect the polymorphism within the MHC DQA in 31 Przewalski's horses from two reintroduced populations. Consequently, only seven alleles were identified, with only four presenting in each population. In comparison with other mammals, the Przewalski's horse demonstrated less MHC variation. The nucleotide genetic distance of the seven ELA-DQA alleles was between 0.012 and 0.161. The Poisson corrected amino acid genetic distance of the founded alleles was 0.01-0.334. The allele and genotype frequencies of both reintroduced populations of Przewalski's horse deviated from the Hardy-Weinberg equilibrium. Specific MHC DQA alleles may have been lost during the extreme bottleneck event that this species underwent throughout history. We suggest the necessity to detect the genetic background of individuals prior to performing the reintroduction project.
主要组织相容性复合体 (MHC) 基因在脊椎动物中是最多态的,许多 MHC 基因的高度变异性被认为在病原体识别中起着至关重要的作用。濒危物种普氏野马的 MHC 类 II 基因座 DQA 多态性进行了分析,普氏野马在野外已经灭绝,目前所有的个体都来自于 12 个祖先。我们使用聚合酶链反应-单链构象多态性(PCR-SSCP)在两个重新引入的普氏野马群体中检测 MHC DQA 内的多态性。结果,仅鉴定出 7 个等位基因,每个群体中仅存在 4 个。与其他哺乳动物相比,普氏野马的 MHC 变异较少。7 个 ELA-DQA 等位基因的核苷酸遗传距离在 0.012 到 0.161 之间。 founders 等位基因的泊松校正氨基酸遗传距离为 0.01-0.334。两个重新引入的普氏野马群体的等位基因和基因型频率均偏离 Hardy-Weinberg 平衡。在该物种经历的极端瓶颈事件中,可能已经失去了特定的 MHC DQA 等位基因。我们建议在进行重新引入项目之前,有必要检测个体的遗传背景。