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Characterization and locus-specific typing of MHC class I genes in the red-billed gull (Larus scopulinus) provides evidence for major, minor, and nonclassical loci

机译:红嘴鸥(Larus scopulinus)中MHC I类基因的表征和基因座特异性分型为主要,次要和非经典基因座提供了证据

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A major challenge facing studies of major histocompatibility complex (MHC) evolution in birds is the difficulty in genotyping alleles at individual loci, and the consequent inability to investigate sequence variation and selection pressures for each gene. In this study, four MHC class I loci were isolated from the red-billed gull (Larus scopulinus), representing both the first characterized MHCI genes within Charadriiformes (shorebirds, gulls, and allies) and the first full-length MHCI sequences described outside Galloanserae (gamebirds + waterfowl). Complete multilocus genotypes were obtained for 470 individuals using a combination of reference-strand conformation analysis and direct sequencing of gene-specific amplification products, and variation of peptide-binding region (PBR) exons was surveyed for all loci. Each gene is transcribed and has conserved sequence features characteristic of antigen-presenting MHCI molecules. However, higher allelic variation, a more even allele frequency distribution, and evidence of positive selection acting on a larger number of PBR residues suggest that only one locus (Lasc-UAA) functions as a major classical MHCI gene. Lasc-UBA, with more limited variation and PBR motifs that encompass a subset of Lasc-UAA diversity, was assigned a putative minor classical function, whereas the divergent and largely invariant binding-groove motifs of Lasc-UCA and -UDA are suggestive of nonclassical loci with specialized ligand-binding roles.
机译:鸟类中主要组织相容性复合体(MHC)进化研究面临的主要挑战是难以对单个位点的等位基因进行基因分型,因此无法研究每个基因的序列变异和选择压力。在这项研究中,从红嘴鸥(Larus scopulinus)分离了四个MHC I类基因座,既代表Charadriiformes内的第一个特征化MHCI基因(shore,海鸥和盟友),又代表Galloanserae外的第一个全长MHCI序列(猎鸟+水禽)。使用参考链构象分析和基因特异性扩增产物的直接测序相结合,获得了470个个体的完整多位点基因型,并调查了所有基因座的肽结合区(PBR)外显子的变异。每个基因被转录并具有抗原呈递MHCI分子特征的保守序列特征。但是,较高的等位基因变异,更均匀的等位基因频率分布以及对大量PBR残基起作用的阳性选择证据表明,只有一个基因座(Lasc-UAA)充当主要的经典MHCI基因。 Lasc-UBA具有更有限的变异和包含Lasc-UAA多样性子集的PBR基序,被分配了一个假定的次要经典功能,而Lasc-UCA和-UDA的发散和很大程度上不变的结合槽基序则暗示了非经典具有专门的配体结合作用的基因座。

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