Evidence map›Paper›PMID 24405759›Full record

ArticleBMC genomics2014

Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals.

Shengjie Yang, Yiyuan Liu, Ning Jiang, Jing Chen, Lindsey Leach, Zewei Luo, Minghui Wang

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Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

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19citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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19 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Shengjie Yang
Yiyuan Liu
Ning Jiang
Jing Chen
Lindsey Leach
Zewei LuoDepartment of Biostatistics and Computational Biology, School of Life Sciences, Laboratory of Population & Quantitative Genetics, State Key Laboratory of Genetic Engineering, Fudan University, Shanghai 200433, China. zwluo@fudan.edu.cn.
Minghui Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile the possible sources underlying the so-called 'missing heritability' evident in current genome-wide association studies (GWAS) of complex traits have been actively pursued in recent years, resolving this mystery remains a challenging task. Studying heritability of genome-wide gene expression traits can shed light on the goal of understanding the relationship between phenotype and genotype. Here we used microarray gene expression measurements of lymphoblastoid cell lines and genome-wide SNP genotype data from 210 HapMap individuals to examine the heritability of gene expression traits.

resultsHeritability levels for expression of 10,720 genes were estimated by applying variance component model analyses and 1,043 expression quantitative loci (eQTLs) were detected. Our results indicate that gene expression traits display a bimodal distribution of heritability, one peak close to 0% and the other summit approaching 100%. Such a pattern of the within-population variability of gene expression heritability is common among different HapMap populations of unrelated individuals but different from that obtained in the CEU and YRI trio samples. Higher heritability levels are shown by housekeeping genes and genes associated with cis eQTLs. Both cis and trans eQTLs make comparable cumulative contributions to the heritability. Finally, we modelled gene-gene interactions (epistasis) for genes with multiple eQTLs and revealed that epistasis was not prevailing in all genes but made a substantial contribution in explaining total heritability for some genes analysed.

conclusionsWe utilised a mixed effect model analysis for estimating genetic components from population based samples. On basis of analyses of genome-wide gene expression from four HapMap populations, we demonstrated detailed exploitation of the distribution of genetic heritabilities for expression traits from different populations, and highlighted the importance of studying interaction at the gene expression level as an important source of variation underlying missing heritability.

Indexed as

Genome, HumanQuantitative Trait, HeritableEpistasis, GeneticGene ExpressionGenome-Wide Association StudyGenotypeHapMap ProjectHumansModels, GeneticPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID24405759
PMCPMC4028055

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.