Zhi-Wei Zhang , Lukas A. Fugmann , Shu Yuan Yang , Jin-Chywan Gwo , Sebastian D. Fugmann
{"title":"The classical MHC class I and II genes of O. m. formosanus exhibit different polymorphism levels","authors":"Zhi-Wei Zhang , Lukas A. Fugmann , Shu Yuan Yang , Jin-Chywan Gwo , Sebastian D. Fugmann","doi":"10.1016/j.dci.2025.105392","DOIUrl":null,"url":null,"abstract":"<div><div><em>Oncorhynchus masou formosanus</em> (Formosan landlocked salmon) is a salmonid fish endemic to Taiwan with a critically endangered extant small population in high-altitude mountain streams. To begin to assess the remaining genetic diversity we characterized the single classical MHC class I (<em>UBA</em>) and MHC class II (<em>DAA</em> and <em>DAB</em>) genes of teleost fish in a small cohort of eight randomly collected <em>O. m. formosanus</em> individuals whose relationship is unknown. We focused on the exons encoding the peptide binding regions of these complexes as they are considered the most highly polymorphic regions in vertebrate genomes. Surprisingly, the <em>DAA</em> and <em>DAB</em> genes appeared homozygous and identical among all eight fish indicating that the encoded class II complex is monomorphic. In contrast, three distinct <em>UBA</em> alleles were discovered with one dominant allele present in every single individual. Notably, 75 % were heterozygous indicating a selective advantage of heterozygosity at this locus. Lastly, our MHC alleles differ from those present in the genome of the closely related Japanese <em>O. m. masou</em>, suggesting that the loss of DAA/DAB diversity and the emergence of the dominant UBA allele occurred after their populations were isolated. Together we discovered residual genetic diversity at the classical MHC class I locus in <em>O. m. formosanus</em> and maintaining this allelic variation unlike the homozygous <em>DAA</em> and <em>DAB</em> genes is likely important for its survival in its geographically restricted unique habitat.</div></div>","PeriodicalId":11228,"journal":{"name":"Developmental and comparative immunology","volume":"168 ","pages":"Article 105392"},"PeriodicalIF":2.7000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental and comparative immunology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0145305X25000813","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
Oncorhynchus masou formosanus (Formosan landlocked salmon) is a salmonid fish endemic to Taiwan with a critically endangered extant small population in high-altitude mountain streams. To begin to assess the remaining genetic diversity we characterized the single classical MHC class I (UBA) and MHC class II (DAA and DAB) genes of teleost fish in a small cohort of eight randomly collected O. m. formosanus individuals whose relationship is unknown. We focused on the exons encoding the peptide binding regions of these complexes as they are considered the most highly polymorphic regions in vertebrate genomes. Surprisingly, the DAA and DAB genes appeared homozygous and identical among all eight fish indicating that the encoded class II complex is monomorphic. In contrast, three distinct UBA alleles were discovered with one dominant allele present in every single individual. Notably, 75 % were heterozygous indicating a selective advantage of heterozygosity at this locus. Lastly, our MHC alleles differ from those present in the genome of the closely related Japanese O. m. masou, suggesting that the loss of DAA/DAB diversity and the emergence of the dominant UBA allele occurred after their populations were isolated. Together we discovered residual genetic diversity at the classical MHC class I locus in O. m. formosanus and maintaining this allelic variation unlike the homozygous DAA and DAB genes is likely important for its survival in its geographically restricted unique habitat.
期刊介绍:
Developmental and Comparative Immunology (DCI) is an international journal that publishes articles describing original research in all areas of immunology, including comparative aspects of immunity and the evolution and development of the immune system. Manuscripts describing studies of immune systems in both vertebrates and invertebrates are welcome. All levels of immunological investigations are appropriate: organismal, cellular, biochemical and molecular genetics, extending to such fields as aging of the immune system, interaction between the immune and neuroendocrine system and intestinal immunity.