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下一代测序和亚利桑那州皮马印第安人完整遗传的经典 HLA 基因座:定义北美古印第安人的核心 HLA 变异。

Next generation sequencing and the classical HLA loci in full heritage Pima Indians of Arizona: Defining the core HLA variation for North American Paleo-Indians.

机构信息

Phoenix Epidemiology and Clinical Research Branch, NIH, NIDDK, Phoenix, AZ 85014, United States.

Phoenix Epidemiology and Clinical Research Branch, NIH, NIDDK, Phoenix, AZ 85014, United States.

出版信息

Hum Immunol. 2019 Dec;80(12):955-965. doi: 10.1016/j.humimm.2019.10.002. Epub 2019 Nov 6.

Abstract

The Pima Indians of the Gila River Indian Community in Arizona have participated in a long-range study of type 2 diabetes mellitus since 1965 and have been the subject of HLA typing and population studies since the early days of serological assays. These data have been in numerous HLA workshops and conferences and have been the source of at least five novel alleles at the classical HLA loci. In recent time nearly the entire study group was subject to next generation sequencing by whole genome or exome technologies, which has allowed us to HLA type over 3000 full heritage persons with recently developed computer algorithms. We present here the results for the classical HLA Loci: HLA-A, B, C, DRA, DRB1, DRB3, DRB4, DRB5, DPA1, DPB1, DQA1, and DQB1 to the third field of resolution for synonymous alleles and type the likely four field resolution alleles from the subset of whole genome sequences. Allele frequencies, and haplotype frequencies at up to five loci, are presented as well as measures of population structure and heterozygosity. We define a core set of HLA variation that approximates the distribution for the Paleo-Indians and impute nine-locus, 4-field haplotypes that are expected to be common in full heritage peoples.

摘要

亚利桑那州希拉河印第安社区的皮马印第安人自 1965 年以来一直参与 2 型糖尿病的长期研究,并自血清学检测早期以来一直是 HLA 分型和人群研究的对象。这些数据已经在许多 HLA 研讨会上进行了讨论,并且至少有五个新的等位基因来源于经典 HLA 基因座。最近,几乎整个研究组都接受了全基因组或外显子组测序技术的检测,这使我们能够使用最近开发的计算机算法对 3000 多名具有完整遗传背景的人进行 HLA 分型。我们在此介绍经典 HLA 基因座的结果:HLA-A、B、C、DRA、DRB1、DRB3、DRB4、DRB5、DPA1、DPB1、DQA1 和 DQB1 的分辨率达到第三等位基因位,以及从全基因组序列中确定的可能具有四等位基因位的亚型。我们还提供了等位基因频率、单倍型频率以及群体结构和杂合度的衡量标准。我们定义了一组 HLA 变异,这些变异近似于古印第安人的分布,并推断了在全基因组人群中常见的九个基因座、四个基因座的单倍型。

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