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英国和爱尔兰区域富集的罕见有害外显子变异体。

Regionally enriched rare deleterious exonic variants in the UK and Ireland.

作者信息

Halachev Mihail, Gountouna Viktoria-Eleni, Meynert Alison, Tzoneva Gannie, Shuldiner Alan R, Semple Colin A, Wilson James F

机构信息

MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Regeneron Genetics Center, Tarrytown, NY, USA.

出版信息

Nat Commun. 2024 Oct 2;15(1):8454. doi: 10.1038/s41467-024-51604-2.

Abstract

It is unclear how patterns of regional genetic differentiation in the UK and Ireland might impact the protein-coding fraction of the genome. We exploit UK Biobank (UKB) and Viking Genes whole exome sequencing data to study regional genetic differentiation across the UK and Ireland in protein coding genes, encompassing 44,696 unrelated individuals from 20 regions of origin. We demonstrate substantial exonic differentiation among Shetlanders, Orcadians, individuals with full or partial Ashkenazi Jewish ancestry and in several mainland regions (particularly north and south Wales, southeast Scotland and Ireland). With stringent filtering criteria, we find 67 regionally enriched (≥5-fold) variants likely to have adverse biomedical consequences in homozygous individuals. Here, we show that regional genetic variation across the UK and Ireland should be considered in the design of genetic studies and may inform effective genetic screening and counselling.

摘要

目前尚不清楚英国和爱尔兰的区域遗传分化模式如何影响基因组的蛋白质编码部分。我们利用英国生物银行(UKB)和维京基因全外显子测序数据,研究英国和爱尔兰蛋白质编码基因的区域遗传分化,涵盖来自20个原籍地区的44,696名无关个体。我们证明了设得兰群岛人、奥克尼群岛人、有全部或部分阿什肯纳兹犹太血统的个体以及几个大陆地区(特别是北威尔士和南威尔士、苏格兰东南部和爱尔兰)之间存在显著的外显子分化。通过严格的筛选标准,我们发现67个区域富集(≥5倍)的变异,这些变异在纯合个体中可能产生不良生物医学后果。在此,我们表明,在遗传研究设计中应考虑英国和爱尔兰的区域遗传变异,这可能为有效的遗传筛查和咨询提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bfd/11446911/77ea80a3c9ce/41467_2024_51604_Fig1_HTML.jpg

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