Evidence map›Paper›PMID 24232670›Full record

ArticleBioMed research international2013

New aQTL SNPs for the CYP2D6 identified by a novel mediation analysis of genome-wide SNP arrays, gene expression arrays, and CYP2D6 activity.

Guanglong Jiang, Arindom Chakraborty, Zhiping Wang, Malaz Boustani, Yunlong Liu, Todd Skaar, Lang Li

Abstract read
In one paragraph

Article in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 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.

Guanglong JiangDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA ; Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Arindom Chakraborty
Zhiping Wang
Malaz Boustani
Yunlong Liu
Todd Skaar
Lang Li

Funding

Indiana PROSPECTR01HS019818 · AHRQ · INDIANA UNIVERSITY INDIANAPOLIS · PI DEXTER, PAUL · 2010 to 2010
$8.4M
Regulation of drug metabolizing enzymes by miRNAsR01GM088076 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI SKAAR, TODD C. · 2009 to 2017
$3.8M
Bayesian Tools for PBPK Models in Drug Onteraction Res.R01GM074217 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI LI, LANG · 2005 to 2009
$1.3M
AHRQ HHS R01 HS019818AHRQ HHS R01 HS019818-01NIGMS NIH HHS R01 GM074217NIGMS NIH HHS R01 GM088076NIGMS NIH HHS R01 GM74217
6 · The paper itself

Abstract

backgroundThe genome-wide association studies (GWAS) have been successful during the last few years. A key challenge is that the interpretation of the results is not straightforward, especially for transacting SNPs. Integration of transcriptome data into GWAS may provide clues elucidating the mechanisms by which a genetic variant leads to a disease.

methodsHere, we developed a novel mediation analysis approach to identify new expression quantitative trait loci (eQTL) driving CYP2D6 activity by combining genotype, gene expression, and enzyme activity data.

results389,573 and 1,214,416 SNP-transcript-CYP2D6 activity trios are found strongly associated (P < 10⁻⁵, FDR = 16.6% and 11.7%) for two different genotype platforms, namely, Affymetrix and Illumina, respectively. The majority of eQTLs are trans-SNPs. A single polymorphism leads to widespread downstream changes in the expression of distant genes by affecting major regulators or transcription factors (TFs), which would be visible as an eQTL hotspot and can lead to large and consistent biological effects. Overlapped eQTL hotspots with the mediators lead to the discovery of 64 TFs.

conclusionsOur mediation analysis is a powerful approach in identifying the trans-QTL-phenotype associations. It improves our understanding of the functional genetic variations for the liver metabolism mechanisms.

Indexed as

Cohort StudiesCytochrome P-450 CYP2D6Gene Expression ProfilingGene Expression Regulation, EnzymologicGenome-Wide Association StudyGenotypeHumansLiverPhenotypePolymorphism, Single NucleotideQuantitative Trait LociTranscriptomeCytochrome P-450 CYP2D6

Identifiers

PMID24232670
PMCPMC3819829

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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.