首页> 外文期刊>European journal of human genetics: EJHG >Sequence diversity of the Rh blood group system in Basques.
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Sequence diversity of the Rh blood group system in Basques.

机译:阵列中RH血型系统的序列变化。

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摘要

Basques show specific cultural, demographic, and genetic characteristics that have placed them as an isolated and unique population within Europe, such as their non-Indo-European language, Euskara. They have historically lived along the Western Pyrenees, between Spain and France, in one of the most important European glacial refugia during the Last Glacial Maximum. The most striking genetic characteristic is their highest frequency of the RhD blood group negative allele, a variant related to the hemolytic disease of the newborn. Both demographic and adaptive processes have been suggested as possible causes of the high frequency of RhD negative in Basques, but neither hypothesis has been clearly demonstrated. While previous studies on the Rh system in Basques have been mostly focused on serological and genotyping diversity, in this work we analyze genotyping and next generation sequencing data in order to provide a general framework of the genetic scenario of the system in Basques. In particular, we genotyped the most relevant variants of the system (D/d, E/e, and C/c), and sequenced three ~6?kb flanking regions surrounding the Rh genes in Basques and also in other populations for comparison. Our results are in agreement with previous studies, with Basques presenting the highest frequency of the RHD deletion (47.2%). Haplotype analyses of D/d, E/e, and C/c variants confirmed an association between the RhC allele, previously suggested to be under positive selection, and the RhD positive variant in non-sub-Saharan populations, including Basques. We also found extreme differentiation for the C/c variant when comparing sub-Saharan to non-sub-Saharan populations.
机译:巴斯克斯表明,将它们作为欧洲内部的孤立和独特的人口放在欧洲,例如他们的非印欧语言,Euskara等特定的文化,人口和遗传特征。他们历史地沿着西班牙和法国之间的西部比利牛斯特生活,在最后一次冰川最大的欧洲最重要的冰川之一中。最引人注目的遗传特征是它们最高频率的RHD血液组负面等位基因,一种与新生儿溶血性疾病有关的变异。已经提出了人口统计和自适应过程,作为巴基尔的高频率的高频频率的可能原因,但没有明确证明假设。虽然以前关于巴斯克的RH系统的研究大多都集中于血清学和基因分型多样性,但在这项工作中,我们分析基因分型和下一代测序数据,以便提供基座中系统的遗传场景的一般框架。特别是,我们基因分为系统的最相关的变体(D / D,E / e和C / C),并测序3〜6?Kb侧翼区域,围绕阵列的Rh基因以及其他群体进行比较。我们的结果与先前的研究一致,基座呈现出RHD缺失的最高频率(47.2%)。 D / D,E / E和C / C变体的单倍型分析证实了RHC等位基因之间的关联,以前建议在阳性选择下,以及非亚撒哈拉群体中的RHD正变体,包括基夸。在将撒哈拉群中与非撒哈拉群体进行比较时,我们还发现对C / C变体的极端分化。

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    Institute of Evolutionary Biology (CSIC - UPF) Departament de Ciències Experimentals i de la Salut;

    Institute for Research in Biomedicine Barcelona Barcelona Spain;

    Department of Viroscience Postgraduate School Molecular Medicine Erasmus MC Rotterdam The;

    Institute of Evolutionary Biology (CSIC - UPF) Departament de Ciències Experimentals i de la Salut;

    Institute of Evolutionary Biology (CSIC - UPF) Departament de Ciències Experimentals i de la Salut;

    Institute of Evolutionary Biology (CSIC - UPF) Departament de Ciències Experimentals i de la Salut;

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  • 正文语种 eng
  • 中图分类 医学遗传学;
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