4.6 Article

Admixture Has Shaped Romani Genetic Diversity in Clinically Relevant Variants

期刊

FRONTIERS IN GENETICS
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fgene.2021.683880

关键词

Romani; whole-exome sequences; clinically relevant variants; drug-response variants; local ancestry inference; Eurocentric bias

资金

  1. Spanish Ministry of Science, Innovation and Universities (MCIU), Agencia Estatal de Investigacion (AEI) [PID2019-106485GBI00/AEI/10.13039/501100011033]
  2. Unidad de Excelencia Maria de Maeztu (AEI) [CEX2018-000792-M]
  3. [FPU17/03501]

向作者/读者索取更多资源

Research findings indicate significant frequency differences in variant distribution between Roma and non-Roma populations, including obesity-related variants associated with South Asian ancestry in Roma and non-insulin dependent diabetes enriched in non-Roma Europeans. Additionally, drug-response variants have increased in Roma, showing clinical associations with metabolic and cardiovascular-related drugs.
Genetic patterns of inter-population variation are a result of different demographic and adaptive histories, which gradually shape the frequency distribution of the variants. However, the study of clinically relevant mutations has a Eurocentric bias. The Romani, the largest transnational minority ethnic group in Europe, originated in South Asia and received extensive gene flow from West Eurasia. Most medical genetic studies have only explored founder mutations related to Mendelian disorders in this population. Here we analyze exome sequences and genome-wide array data of 89 healthy Spanish Roma individuals to study complex traits and disease. We apply a different framework and focus on variants with both increased and decreased allele frequencies, taking into account their local ancestry. We report several OMIM traits enriched for genes with deleterious variants showing increased frequencies in Roma or in non-Roma (e.g., obesity is enriched in Roma, with an associated variant linked to South Asian ancestry; while non-insulin dependent diabetes is enriched in non-Roma Europeans). In addition, previously reported pathogenic variants also show differences among populations, where some variants segregating at low frequency in non-Roma are virtually absent in the Roma. Lastly, we describe frequency changes in drug-response variation, where many of the variants increased in Roma are clinically associated with metabolic and cardiovascular-related drugs. These results suggest that clinically relevant variation in Roma cannot only be characterized in terms of founder mutations. Instead, we observe frequency differences compared to non-Roma: some variants are absent, while other have drifted to higher frequencies. As a result of the admixture events, these clinically damaging variants can be traced back to both European and South Asian-related ancestries. This can be attributed to a different prevalence of some genetic disorders or to the fact that genetic susceptibility variants are mostly studied in populations of European descent, and can differ in individuals with different ancestries.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据