Department of Psychiatry, University of California San Diego, La Jolla, California, USA.
Department of Internal Medicine, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, North Carolina, USA.
Genes Brain Behav. 2024 Aug;23(4):e12909. doi: 10.1111/gbb.12909.
Delay 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.
延迟折扣是指随着奖励接收时间的延迟而降低奖励价值的行为倾向。延迟折扣增加与物质使用障碍和多种共病精神病理学有关。人类和动物遗传学研究已经确定延迟折扣是可遗传的,但只确定了少数相关基因。我们旨在通过全基因组关联研究(GWAS)识别与延迟折扣相关的新遗传位点,使用杂种(HS)大鼠,这是一种源自八个近交系的遗传多样化的远交种群。我们使用调整数量程序评估 650 只雄性和雌性 HS 大鼠的延迟折扣,在该程序中,大鼠在较小的即时蔗糖奖励或各种延迟的较大奖励之间进行选择。计算偏好切换点,并对这些无差异点拟合指数和双曲线函数。两种函数的曲线下面积(AUC)和折扣参数 k 都用作延迟折扣的度量。AUC、指数 k 和一个无差异点的 GWAS 确定了染色体 20 和 14 上的显著位点。编码溶质载体家族成员的 Slc35f1 基因是染色体 20 位点内的唯一基因。该基因座还包含 Slc35f1 的 eQTL,这表明遗传差异表达可能是与行为相关的原因。编码 latrophilin 亚家族 G 蛋白偶联受体的 Adgrl3 是染色体 14 基因座内的唯一基因。这些发现表明在延迟折扣中涉及新基因,并强调需要进一步探索。