Genome‐wide association study of delay discounting in Heterogeneous Stock rats

Author:

Lara Montana Kay1,Chitre Apurva S.1,Chen Denghui1,Johnson Benjamin B.1,Nguyen Khai‐Minh1,Cohen Katarina A.1,Muckadam Sakina A.1,Lin Bonnie1,Ziegler Shae1,Beeson Angela2,Sanches Thiago M.1,Solberg Woods Leah C.2ORCID,Polesskaya Oksana1,Palmer Abraham A.13,Mitchell Suzanne H.4

Affiliation:

1. Department of Psychiatry University of California San Diego La Jolla California USA

2. Department of Internal Medicine, Wake Forest School of Medicine Wake Forest University Winston‐Salem North Carolina USA

3. Institute for Genomic Medicine University of California San Diego La Jolla California USA

4. Department of Behavioral Neuroscience, Psychiatry, the Oregon Institute of Occupational Health Sciences Oregon Health & Science University Portland Oregon USA

Abstract

AbstractDelay discounting refers to the behavioral tendency to devalue rewards as a function of their delay in receipt. Heightened delay discounting has been associated with substance use disorders and multiple co‐occurring psychopathologies. Human and animal genetic studies have established that delay discounting is heritable, but only a few associated genes have been identified. We aimed to identify novel genetic loci associated with delay discounting through a genome‐wide association study (GWAS) using Heterogeneous Stock (HS) rats, a genetically diverse outbred population derived from eight inbred founder strains. We assessed delay discounting in 650 male and female HS rats using an adjusting amount procedure in which rats chose between smaller immediate sucrose rewards or a larger reward at various delays. Preference switch points were calculated and both exponential and hyperbolic functions were fitted to these indifference points. Area under the curve (AUC) and the discounting parameter k of both functions were used as delay discounting measures. GWAS for AUC, exponential k, and one indifference point identified significant loci on chromosomes 20 and 14. The gene Slc35f1, which encodes a member of the solute carrier family, was the sole gene within the chromosome 20 locus. That locus also contained an eQTL for Slc35f1, suggesting that heritable differences in the expression might be responsible for the association with behavior. Adgrl3, which encodes a latrophilin subfamily G‐protein coupled receptor, was the sole gene within the chromosome 14 locus. These findings implicate novel genes in delay discounting and highlight the need for further exploration.

Publisher

Wiley

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