Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change

Author:

Mohammadi Pejman,Castel Stephane E.,Brown Andrew A.,Lappalainen Tuuli

Abstract

Mapping cis-acting expression quantitative trait loci (cis-eQTL) has become a popular approach for characterizing proximal genetic regulatory variants. In this paper, we describe and characterize log allelic fold change (aFC), the magnitude of expression change associated with a given genetic variant, as a biologically interpretable unit for quantifying the effect size of cis-eQTLs and a mathematically convenient approach for systematic modeling of cis-regulation. This measure is mathematically independent from expression level and allele frequency, additive, applicable to multiallelic variants, and generalizable to multiple independent variants. We provide efficient tools and guidelines for estimating aFC from both eQTL and allelic expression data sets and apply it to Genotype Tissue Expression (GTEx) data. We show that aFC estimates independently derived from eQTL and allelic expression data are highly consistent, and identify technical and biological correlates of eQTL effect size. We generalize aFC to analyze genes with two eQTLs in GTEx and show that in nearly all cases the two eQTLs act independently in regulating gene expression. In summary, aFC is a solid measure of cis-regulatory effect size that allows quantitative interpretation of cellular regulatory events from population data, and it is a valuable approach for investigating novel aspects of eQTL data sets.

Funder

Common Fund of the Office of the Director of the National Institutes of Health

NCI, NHGRI, NHLBI, NIDA, NIMH and NINDS

NCI\SAIC-Frederick

National Disease Research Interchange

Roswell Park Cancer Institute

Science Care

The Broad Institute

SAIC-F subcontract to Van Andel Institute

SAIC-F

University of Miami

University of Geneva

University of Chicago

University of North Carolina–Chapel Hill

Harvard University

Stanford University

Washington University St Louis

University of Pennsylvania

NIH

Publisher

Cold Spring Harbor Laboratory

Subject

Genetics (clinical),Genetics

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