通过下一代测序评估俄罗斯人群HLA多样性

E. Khamaganova, E. Leonov, A. Abdrakhimova, S. Khizhinskiy, T. Gaponova, V. Savchenko
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引用次数: 1

摘要

下一代测序用于以4域(等位基因)分辨率确定HLA基因的全长序列。这项研究旨在确定国家血液学研究中心注册处的一组献血者中HLA等位基因的频率和多样性,这些献血者将自己设计成俄罗斯人(包括HLA基因区域的一些非常规分型变异)。研究人群包括1510名捐赠者。通过下一代测序进行HLA分型。使用AllType NGS扩增试剂盒(One Lambda,USA)进行文库扩增,并使用MiSeq(Illumina,USA)测序。数据分析使用TypeStream Visual Software V2.0.0.68(One Lambda,USA)和IPD-IMGT/HLA数据库3.40.0.1。Arlequin 3.5软件用于估计等位基因和单倍型频率,偏离Hardy-Weinberg平衡。用四场分辨法鉴定出82个HLA-A、156个HLA-В和85个HLA-С等位基因。经2~3区分辨,共鉴定出45个HLA-DRB1和18个HLA-DQB1等位基因。在自称俄罗斯人的捐献者中发现了相当大的HLA多样性:该人群在每个HLA基因上都有大量不同的等位基因,高百分比的等位突变(HLA I类的25-32%)只出现过一次。IPD-IMGT/HLA数据库中没有足够数量的新等位基因。俄罗斯人群中相当大的等位基因多样性是由于低发病率等位基因。尽管存在这种多样性,但在每个基因座检测到的大多数HLA等位基因是常见的。供体HLA的显著多样性与大量罕见的等位基因有关。在我们的研究中发现的新等位基因与已知等位基因的单核苷酸取代不同。在四个领域水平上,最常见的等位基因如下:A*02:01:01:01(27.1%),C*07:02:01:03(13.1%),A*03:01:01:00(13.0%),B*07:02:201:01(13.0%。本研究中获得的数据可作为参考样本,用于估计俄罗斯人群中HLA等位基因的频率,在寻找异基因造血干细胞移植供体时对特定等位基因进行适当的频率评估,以及HLA等位蛋白与不同疾病之间的关联研究,以及人群遗传学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HLA diversity in the Russian population assessed by next generation sequencing
Next generation sequencing is used to determine full-length sequences of HLA genes at the 4-field (allelic) resolution. The study was aimed at determining frequency and diversity of HLA alleles in a cohort of blood donors from the Registry of the National Research Center for Hematology who design ated themselves as Russians (including some not routinely typed variations in HLA gene regions). The studied population consisted of 1510 donors. HLA typing was performed by next generation sequencing. Libraries were performed with AllType NGS Amplification Kits (One Lambda, USA) and sequenced using MiSeq (Illumina, USA). Data analysis used the TypeStream Visual Software V2.0.0.68 (One Lambda, USA) and IPD-IMGT/HLA database 3.40.0.1. Arlequin 3.5 software was used for estimation of allele and haplotype frequencies, deviation from Hardy-Weinberg equilibrium. 82 HLA-A, 156 HLA-В and 85 HLA-С alleles were identified with four-field resolution. 45 HLA-DRB1 and 18 HLA-DQB1 alleles were identified with 2-3-field resolution. Considerable HLA diversity was found among the donors self-designated as Russians: the population had large numbers of distinct alleles at each HLA gene, high percentage of alleles (25-32% of HLA class I) were revealed only once. Sufficient numbers of new alleles were registered which are absent in the IPD-IMGT/HLA database. Considerable allelic diversity in Russian population is due to low-incidence alleles. Despite this diversity, the majority of HLA alleles detected at each locus were common. Significant HLA diversity of the donors was connected with a large number of alleles with rare occurrence. The novel alleles identified in our study differed from the known alleles by single nucleotide substitutions. The most common alleles at the four-field level were as follows: A*02:01:01:01 (27.1%), C*07:02:01:03 (13.1%), A*03:01:01:01 (13.0%), B*07:02:01:01 (13.0%), A*01:01:01:01 (11.6%) and C*07:01:01:01/16 (10.4%). The HLA alleles, which are common for Russian populations, are not always common or well-documented alleles in present catalogues. The data obtained in this study may be used as a reference sample for estimation of HLA allele frequencies in Russian population, for proper frequency evaluation of specific alleles when searching donors for allogeneic hematopoietic stem cell transplantation, as well as for association studies between HLA alleles and different diseases, and for research in population genetics.
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