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分析 RNF213 中 R4810K 风险等位基因在烟雾病中的人口历史。

An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.

机构信息

Department of Biological Structure, Kitasato University Graduate School of Medical Sciences, Sagamihara, Kanagawa, Japan.

Faculty of Medicine, Advanced Medical Research Center, University of the Ryukyus, Nishihara, Okinawa, Japan.

出版信息

Ann Hum Genet. 2021 Sep;85(5):166-177. doi: 10.1111/ahg.12424. Epub 2021 May 20.

Abstract

BACKGROUND

Ring finger protein 213 (RNF213) is a susceptibility gene of moyamoya disease (MMD). A previous case-control study and a family analysis demonstrated a strong association of the East Asian-specific variant, R4810K (rs112735431), with MMD. Our aim is to uncover evolutionary history of R4810K in East Asian populations.

METHODS

The RNF213 locus of 24 MMD patients in Japan were sequenced using targeted-capture sequencing. Based on the sequence data, we conducted population genetic analysis and estimated the age of R4810K using coalescent simulation.

RESULTS

The diversity of the RNF213 gene was higher in Africans than non-Africans, which can be explained by bottleneck effect of the out-of-Africa migration. Coalescent simulation showed that the risk variant was born in East Asia 14,500-5100 years ago and came to the Japanese archipelago afterward, probably in the period when the known migration based on archaeological evidences occurred.

CONCLUSIONS

Although clinical data show that the symptoms varies, all sequences harboring the risk allele are almost identical with a small number of exceptions, suggesting the MMD phenotypes are unaffected by the variants of this gene and rather would be more affected by environmental factors.

摘要

背景

环指蛋白 213(RNF213)是烟雾病(MMD)的易感基因。先前的病例对照研究和家系分析表明,东亚特有的变体 R4810K(rs112735431)与 MMD 强烈相关。我们的目的是揭示 R4810K 在东亚人群中的进化历史。

方法

使用靶向捕获测序对 24 名日本 MMD 患者的 RNF213 基因座进行测序。基于序列数据,我们进行了群体遗传分析,并使用合并模拟估计了 R4810K 的年龄。

结果

非洲人的 RNF213 基因多样性高于非非洲人,这可以用非洲人外迁的瓶颈效应来解释。合并模拟表明,风险变异在 14500-5100 年前出现在东亚,之后出现在日本列岛,可能在已知的基于考古证据的迁徙时期。

结论

尽管临床数据显示症状不同,但所有携带风险等位基因的序列几乎完全相同,只有少数例外,这表明 MMD 表型不受该基因变异的影响,而更受环境因素的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc20/8453937/255595d01239/AHG-85-166-g002.jpg

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