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结构多态性Alu插入序列与HLA - A、- B和 - C等位基因以及MHC I类区域内其他逆转录元件之间的遗传变异与搭便车效应。

Genetic variation and hitchhiking between structurally polymorphic Alu insertions and HLA-A, -B, and -C alleles and other retroelements within the MHC class I region.

作者信息

Kulski J K, Shigenari A, Inoko H

机构信息

Centre for Forensic Science, The University of Western Australia, Nedlands, WA 6008, Australia.

出版信息

Tissue Antigens. 2011 Nov;78(5):359-77. doi: 10.1111/j.1399-0039.2011.01776.x.

Abstract

We investigated structurally polymorphic Alu insertions (POALINs) at five loci in the major histocompatibility complex (MHC) class I genomic region to determine their allele and haplotype frequencies and associations with the human leukocyte antigen (HLA)-A, -B, and -C genes in three populations, the Australian Caucasians, Japanese, and African Americans. The POALINs varied in allelic frequency between 0% and 42.3% with significant differences between populations at three of the five loci. The linkage disequilibrium (LD) between Alu insertions and the HLA-A, -B, or -C alleles and previously published polymorphic retroelements (four SVA and human endogenous retrovirus type 9 (HERVK9) loci) within the class I region of the MHC were calculated in pairwise analyses of haplotypes to show strong allelic associations and possible crossing-over events between some loci. Each POALIN was in significant LD with a variety of HLA-A, -B, or -C two-digit alleles probably as a result of hitchhiking. The POALINs helped to further stratify the HLA-A:B:C haplotypes into different POALIN:HLA-A:B:C haplotype frequencies. Of the multilocus haplotype analyses, the seven- and eight-locus haplotypes showed the largest number of differences between the populations, and fewer matched haplotypes between populations that ranged, for example, from 49% for HLA-B:HLA-A haplotypes to 7% for AluMICB:HLA-B:HLA-C:AluTF:AluHJ:HLA-A:AluHG:AluTF haplotypes in the Japanese. This comparative study of multilocus POALINs in the HLA class I region of three ethnic populations shows that POALINs alone or together with the HLA class I alleles and other retroelements are informative ancestral markers for assessing the interrelationship of HLA class I haplotype lineages, LD, and genetic diversity within the same and/or different populations.

摘要

我们研究了主要组织相容性复合体(MHC)I类基因组区域中五个位点的结构多态性Alu插入序列(POALINs),以确定它们在澳大利亚白种人、日本人及非裔美国人这三个人群中的等位基因和单倍型频率,以及与人类白细胞抗原(HLA)-A、-B和-C基因的关联。POALINs的等位基因频率在0%至42.3%之间变化,五个位点中的三个位点在不同人群间存在显著差异。通过对单倍型进行成对分析,计算了Alu插入序列与HLA-A、-B或-C等位基因以及MHC I类区域内先前公布的多态性逆转录元件(四个SVA和人类内源性逆转录病毒9型(HERVK9)位点)之间的连锁不平衡(LD),结果显示某些位点之间存在强烈的等位基因关联和可能的交叉事件。每个POALIN与多种HLA-A、-B或-C两位数字等位基因存在显著的LD,这可能是搭便车效应的结果。POALINs有助于将HLA-A:B:C单倍型进一步分层为不同的POALIN:HLA-A:B:C单倍型频率。在多位点单倍型分析中,七位点和八位点单倍型在不同人群间显示出最多的差异,不同人群间匹配的单倍型较少,例如在日本人中,HLA-B:HLA-A单倍型的匹配率为49%,而AluMICB:HLA-B:HLA-C:AluTF:AluHJ:HLA-A:AluHG:AluTF单倍型的匹配率为7%。这项对三个人群HLA I类区域中多位点POALINs的比较研究表明,单独的POALINs或与HLA I类等位基因及其他逆转录元件一起,都是用于评估同一和/或不同人群中HLA I类单倍型谱系、LD和遗传多样性相互关系的有用祖先标记。

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