Okano Masaharu, Miyamae Jiro, Suzuki Shingo, Nishiya Kohei, Katakura Fumihiko, Kulski Jerzy K, Moritomo Tadaaki, Shiina Takashi
Department of Veterinary Medicine, College of Bioresource Sciences, Nihon University, Fujisawa, Japan.
Faculty of Veterinary Medicine, Okayama University of Science, Imabari, Japan.
Front Genet. 2020 Jul 15;11:750. doi: 10.3389/fgene.2020.00750. eCollection 2020.
The major histocompatibility complex (MHC) is a highly polymorphic and duplicated genomic region that encodes transplantation and immune regulatory molecules. Although it is well-known that particular MHC allelic polymorphisms and haplotypes are genetically relate to immune-mediated diseases detailed information of the cat MHC (Feline Leukocyte Antigen; FLA) genetic and haplotypic structure and diversity is limited in comparison to humans and many other species. In this study, to better understand the degree and types of allele and allelic haplotype diversity of FLA-class I (FLA-I) and FLA-DRB loci in domestic cats, we identified six expressible FLA-I loci in peripheral white blood cells by estimation of the coding exons and NGS-based amplicon sequencing using five unrelated cats. We then used a newly developed NGS-based genotyping method to genotype and annotate 32 FLA-I and 16 FLA-DRB sequences in two families of 20 domestic cats. A total of 14 FLA-I and seven FLA-DRB were identified as novel polymorphic sequences. Phylogenetic analyses grouped the sequences into six FLA-I (FLA-E/H/K, FLA-A, FLA-J, FLA-L, FLA-O and a tentatively named FLA-E/H/K_Rec) and four FLA-DRB (FLA-DRB1, FLA-DRB3, FLA-DRB4, and FLA-DRB5) lineages. Pedigree analysis of two cat families revealed eight distinct FLA structural haplotypes (Class I - DRB) with five to eight FLA-I and two to three FLA-DRB transcribed loci per haplotype. It is evident that the eight FLA haplotypes were generated by gene duplications and deletions, and rearrangements by genetic recombination with the accumulation and/or inheritance of novel polymorphisms. These findings are useful for further genetic diversity analysis and disease association studies among cat breeds and in veterinary medicine.
主要组织相容性复合体(MHC)是一个高度多态且重复的基因组区域,编码移植和免疫调节分子。尽管众所周知,特定的MHC等位基因多态性和单倍型与免疫介导的疾病存在遗传关联,但与人类和许多其他物种相比,猫MHC(猫白细胞抗原;FLA)的遗传和单倍型结构及多样性的详细信息有限。在本研究中,为了更好地了解家猫中FLA - I类(FLA - I)和FLA - DRB基因座的等位基因及等位基因单倍型多样性的程度和类型,我们通过对五个无亲缘关系的猫的编码外显子进行估计,并使用基于二代测序(NGS)的扩增子测序,在周边白细胞中鉴定出六个可表达的FLA - I基因座。然后,我们使用一种新开发的基于NGS的基因分型方法,对20只家猫的两个家系中的32个FLA - I和16个FLA - DRB序列进行基因分型和注释。总共鉴定出14个FLA - I和7个FLA - DRB为新的多态性序列。系统发育分析将这些序列分为六个FLA - I(FLA - E/H/K、FLA - A、FLA - J、FLA - L、FLA - O以及一个暂命名为FLA - E/H/K_Rec)和四个FLA - DRB(FLA - DRB1、FLA - DRB3、FLA - DRB4和FLA - DRB5)谱系。对两个猫家族的系谱分析揭示了八种不同的FLA结构单倍型(I类 - DRB),每个单倍型有五到八个FLA - I和两到三个FLA - DRB转录基因座。显然,这八种FLA单倍型是通过基因复制、缺失以及遗传重组导致的重排,并伴随着新多态性的积累和/或遗传而产生的。这些发现对于进一步分析猫品种之间的遗传多样性以及开展兽医学中的疾病关联研究具有重要意义。