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汉族人群肝脏表达定量性状基因座(eQTLs)的定位

Mapping of hepatic expression quantitative trait loci (eQTLs) in a Han Chinese population.

作者信息

Wang Xiaoliang, Tang Huamei, Teng Mujian, Li Zhiqiang, Li Jianguo, Fan Junwei, Zhong Lin, Sun Xing, Xu Junming, Chen Guoqing, Chen Dawei, Wang Zhaowen, Xing Tonghai, Zhang Jinyan, Huang Li, Wang Shuyun, Peng Xiao, Qin Shengying, Shi Yongyong, Peng Zhihai

机构信息

Department of General Surgery, Shanghai First People's Hospital, Medical College, Shanghai Jiaotong University, Shanghai, China.

出版信息

J Med Genet. 2014 May;51(5):319-26. doi: 10.1136/jmedgenet-2013-102045. Epub 2014 Mar 24.

Abstract

BACKGROUND

Elucidating the genetic basis underlying hepatic gene expression variability is of importance to understand the aetiology of the disease and variation in drug metabolism. To date, no genome-wide expression quantitative trait loci (eQTLs) analysis has been conducted in the Han Chinese population, the largest ethnic group in the world.

METHODS

We performed a genome-wide eQTL mapping in a set of Han Chinese liver tissue samples (n=64). The data were then compared with published eQTL data from a Caucasian population. We then performed correlations between these eQTLs with important pharmacogenes, and genome-wide association study (GWAS) identified single nucleotide polymorphisms (SNPs), in particular those identified in the Asian population.

RESULTS

Our analyses identified 1669 significant eQTLs (false discovery rate (FDR) < 0.05). We found that 41% of Asian eQTLs were also eQTLs in Caucasians at the genome-wide significance level (p=10⁻⁸). Both cis- and trans-eQTLs in the Asian population were also more likely to be eQTLs in Caucasians (p<10⁻⁴). Enrichment analyses revealed that trait-associated GWAS-SNPs were enriched within the eQTLs identified in our data, so were the GWAS-SNPs specifically identified in Asian populations in a separate analysis (p<0.001 for both). We also found that hepatic expression of very important pharmacogenetic (VIP) genes (n=44) and a manually curated list of major genes involved in pharmacokinetics (n=341) were both more likely to be controlled by eQTLs (p<0.002 for both).

CONCLUSIONS

Our study provided, for the first time, a comprehensive hepatic eQTL analysis in a non-European population, further generating valuable data for characterising the genetic basis of human diseases and pharmacogenetic traits.

摘要

背景

阐明肝脏基因表达变异性的遗传基础对于理解疾病病因和药物代谢差异具有重要意义。迄今为止,尚未在世界上最大的民族——汉族人群中进行全基因组表达定量性状位点(eQTL)分析。

方法

我们对一组汉族肝脏组织样本(n = 64)进行了全基因组eQTL定位。然后将数据与来自高加索人群的已发表eQTL数据进行比较。接着我们对这些eQTL与重要药物代谢基因进行相关性分析,并对全基因组关联研究(GWAS)鉴定出的单核苷酸多态性(SNP),特别是在亚洲人群中鉴定出的那些SNP进行分析。

结果

我们的分析鉴定出1669个显著的eQTL(错误发现率(FDR)< 0.05)。我们发现,在全基因组显著水平(p = 10⁻⁸)下,41%的亚洲eQTL在高加索人群中也是eQTL。亚洲人群中的顺式和反式eQTL在高加索人群中也更有可能是eQTL(p < 10⁻⁴)。富集分析表明,性状相关的GWAS-SNP在我们数据中鉴定出的eQTL内富集,在单独分析中在亚洲人群中特异性鉴定出的GWAS-SNP也是如此(两者p < 0.001)。我们还发现,非常重要的药物代谢基因(VIP)(n = 44)的肝脏表达以及一份人工整理的参与药代动力学的主要基因列表(n = 341)都更有可能受eQTL控制(两者p < 0.002)。

结论

我们的研究首次在非欧洲人群中提供了全面的肝脏eQTL分析,进一步生成了用于表征人类疾病和药物代谢性状遗传基础的有价值数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/724b/3995251/43fa74114235/jmedgenet-2013-102045f01.jpg

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