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

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 pop...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995251/
https://www.ncbi.nlm.nih.gov/pubmed/24665059
http://dx.doi.org/10.1136/jmedgenet-2013-102045
Descripción
Sumario: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.