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对阿尔茨海默病东亚特异性遗传风险位点的功能洞察。

Functional insight into East Asian-specific genetic risk loci for Alzheimer's disease.

作者信息

Cho Minyoung, Chaudhuri Soumilee, Liu Shiwei, Park Tamina, Huang Yen-Ning, Rosewood Thea, Bice Paula J, Saykin Andrew J, Won Hong-Hee, Nho Kwangsik

机构信息

Center for Neuroimaging, Department of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Indiana Alzheimer's Disease Research Center, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

Alzheimers Dement. 2025 Feb;21(2):e14553. doi: 10.1002/alz.14553.

Abstract

INTRODUCTION

The functional study of genetic risk factors for Alzheimer's disease (AD) provides insights into the underlying mechanisms and identification of potential therapeutic targets. Investigating AD-associated genetic loci identified in East Asian populations using single-nucleus RNA-sequencing data may identify novel functional genetic contributors.

METHODS

Cell type-specific expression quantitative trait loci (eQTL) and peak-to-gene links were used to identify functional genes associated with 26 genetic loci from seven genome-wide association studies (GWAS) for AD in East Asians.

RESULTS

KCNJ6 and MAPK1IP1L were identified as significant eQTLs with AD risk loci. AD risk loci were in peaks related to four genes, with CLIC4 being connected across different cell types. Genes identified in European and East Asian GWAS interacted within networks and were enriched in AD pathology pathways in astrocytes.

DISCUSSION

Our findings suggest KCNJ6 and CLIC4 as novel AD-associated functional genes, providing insight into the genetic architecture of AD in East Asians.

HIGHLIGHTS

Integrated functional analysis of Alzheimer's disease (AD) loci in seven East Asian genome-wide association studies (GWAS) was performed. Cell type-specific expression quantitative trait loci (eQTLs) and assay for transposase-accessible chromatin peaks were used to identify AD functional genes. An AD risk variant was linked to KCNJ6 through an oligodendrocyte progenitor cell-specific eQTL. An AD risk variant maps to open chromatin, linked to CLIC4 across six cell types. Astrocyte differentially expressed genes by AD pathology are enriched in East Asian and European GWAS genes.

摘要

引言

对阿尔茨海默病(AD)遗传风险因素的功能研究有助于深入了解其潜在机制并确定潜在的治疗靶点。利用单核RNA测序数据研究在东亚人群中鉴定出的与AD相关的基因位点,可能会发现新的功能性遗传贡献因素。

方法

利用细胞类型特异性表达数量性状基因座(eQTL)和峰-基因联系,从七项针对东亚人AD的全基因组关联研究(GWAS)中鉴定与26个基因位点相关的功能基因。

结果

KCNJ6和MAPK1IP1L被鉴定为与AD风险位点相关的显著eQTL。AD风险位点位于与四个基因相关的峰中,CLIC4在不同细胞类型间存在联系。在欧洲和东亚GWAS中鉴定出的基因在网络内相互作用,并在星形胶质细胞的AD病理途径中富集。

讨论

我们的研究结果表明KCNJ6和CLIC4是新的与AD相关的功能基因,为东亚人AD的遗传结构提供了见解。

亮点

对七项东亚全基因组关联研究(GWAS)中的阿尔茨海默病(AD)基因座进行了综合功能分析。利用细胞类型特异性表达数量性状基因座(eQTL)和转座酶可及染色质峰分析来鉴定AD功能基因。一个AD风险变异通过少突胶质细胞前体细胞特异性eQTL与KCNJ6相关联。一个AD风险变异映射到开放染色质,在六种细胞类型中与CLIC4相关联。AD病理导致的星形胶质细胞差异表达基因在东亚和欧洲GWAS基因中富集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75a2/11848548/3232f540b939/ALZ-21-e14553-g003.jpg

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