Introduction
Overview
Teaching: 10 min
Exercises: 10 minQuestions
What are expression quantitative trait loci (eQTL)?
How are eQTL used in genetic studies?
Objectives
Describe how an expression quantitative trait locus (eQTL) impacts gene expression.
Describe how eQTL are used in genetic studies.
Genome variability influences differential disease risk among individuals. Identifying the effects of genome variants is key to understanding disease biology or organismal phenotype. The effects of variants in many single-gene disorders, such as cystic fibrosis, are generally well-characterized and their disease biology well understood. In cystic fibrosis for example, mutations in the coding region of the CFTR gene alters the three-dimensional structure of resulting chloride channel proteins in epithelial cells, affecting not only chloride transport but also sodium and potassium transport in the lungs, pancreas and skin. The path from gene mutation to altered protein to disease phenotype is relatively simple and well understood.
The most common human disorders, however, involve many genes interacting with the environment and with one another, a far more complicated path to follow than the path from a single gene mutation to its resulting protein to a disease phenotype. Cardiovascular disease, Alzheimer’s disease, arthritis, diabetes and cancer involve a complex interplay of genes with environment, and their mechanisms are not well understood. Genome-wide association studies (GWAS) associate genetic loci with disease traits, yet most GWAS variants for common diseases like diabetes are located in non-coding regions of the genome. These variants are therefore likely to be involved in gene regulation.
Gene regulation controls the quantity, timing and locale of gene expression. Analyzing genome variants through cell or tissue gene expression is known as expression quantitative trait locus (eQTL) analysis. An eQTL is a locus associated with expression of a gene or genes. An eQTL explains some of the variation in gene expression. Specifically, genetic variants underlying eQTL explain variation in gene expression levels. eQTL studies can reveal the architecture of quantitative traits, connect DNA sequence variation to phenotypic variation, and shed light on transcriptional regulation and regulatory variation. Traditional analytic techniques like linkage and association mapping can be applied to thousands of gene expression traits (transcripts) in eQTL analysis, such that gene expression can be mapped in much the same way as a physiological phenotype like blood pressure or heart rate. Joining gene expression and physiological phenotypes with genetic variation can uncover genes with variants affecting disease phenotypes.
To the simple diagram above we’ll add two more details. Non-coding SNPs can regulate gene expression from nearby on the same chromosome (in cis):
SNPs that affect gene expression from afar, often from a different chromosome from the gene that they regulate are called trans regulators.
In this lesson we revisit genetic mapping of quantitative traist and apply its methods to gene expression. The examples are from Genetic Drivers of Pancreatic Islet Function by Keller, et al. This study offers supporting evidence for type 2 diabetes-associated loci in human GWAS, most of which affect pancreatic islet function. The study assessed pancreatic islet gene expression in Diversity Outbred mice on either a regular chow or high-fat high-sugar diet. Islet mRNA abundance was quantified and analyzed, and the study identified more than 18,000 eQTL.
What are eQTL?
With a partner, discuss
- your understanding of eQTL.
- how mutations result in eQTL and ultimately in disease phenotypes.
- the methods that can be used for eQTL analysis.
Solution
Key Points
An expression quantitative trait locus (eQTL) explains part of the variation in gene expression.
Traditional linkage and association mapping can be applied to gene expression traits (transcripts).
Genetic variants, such as single nucleotide polymorphisms (SNPs), that underlie eQTL illuminate transcriptional regulation and variation.