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亚利桑那州全血统皮马印第安人的 HLA 基因座的新一代测序,第二部分:HLA-A、-B 和 -C 以及全基因组序列中 4 个字段分辨率下的选定非经典基因座。

Next generation sequencing for HLA loci in full heritage Pima Indians of Arizona, Part II: HLA-A, -B, and -C with selected non-classical loci at 4-field resolution from whole genome sequences.

机构信息

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

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

出版信息

Hum Immunol. 2021 Jun;82(6):385-403. doi: 10.1016/j.humimm.2021.03.013. Epub 2021 Apr 17.

Abstract

While the samples and data from the Pima Indians of the Gila River Indian Community have been included in many international HLA workshops and conferences and have been the focus of numerous population reports and the source of novel alleles at the classical HLA loci, they have not been studied for the non-classical loci. In order to expand our HLA-disease association studies, we typed over 300 whole genome sequences from full Pima heritage members, controlled for first degree relationship, and employed recently developed computer algorithms to resolve HLA alleles. Both classical-HLA-A, -B, and -C- and non-classical- HLA-E, -F, -G, -J, -L, -W, -Y, -DPA2, -DPB2, -DMA, -DMB, -DOA, -DRB2, -DRB9, TAP1- loci were typed at the 4-field level of resolution. We present allele and selected haplotype frequencies, test the genotype distributions for population structure, discuss the issues that are created for tests of Hardy-Weinberg equilibrium over the four sample spaces of high resolution HLA typing, and address the implications for the evolution of non-classical pseudogenes that are no longer expressed in a phenotype subject to natural selection.

摘要

虽然来自希拉河印第安社区皮马印第安人的样本和数据已经被纳入了许多国际 HLA 研讨会和会议,并成为了许多人群报告的焦点,也是经典 HLA 基因座新型等位基因的来源,但它们尚未在非经典基因座上进行研究。为了扩展我们的 HLA 疾病关联研究,我们对超过 300 名具有完整皮马血统的成员进行了全基因组测序,这些成员经过一级亲属关系控制,并采用了最近开发的计算机算法来解析 HLA 等位基因。我们对经典 HLA-A、-B 和 -C-和非经典 HLA-E、-F、-G、-J、-L、-W、-Y、-DPA2、-DPB2、-DMA、-DMB、-DOA、-DRB2、-DRB9、TAP1 基因座进行了 4 字段分辨率的分型。我们展示了等位基因和选定的单倍型频率,检验了基因型在人群结构中的分布,讨论了在高分辨率 HLA 分型的四个样本空间中进行哈迪-温伯格平衡检验所产生的问题,并探讨了对非经典假基因的进化影响,这些假基因不再在受自然选择影响的表型中表达。

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