A social encounter drives gene expression changes linked to neuronal function, brain development, and related disorders in mice expressing the serotonin transporter Ala56 variant

• Published in: Neuroscience letters Vol. 730; p. 135027
• Main Authors: O’Reilly, Kally C., Anacker, Allison M.J., Rogers, Tiffany D., Forsberg, C. Gunnar, Wang, Jing, Zhang, Bing, Blakely, Randy D., Veenstra-VanderWeele, Jeremy
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 21.06.2020
• Subjects: Amygdala; Animals; Autism spectrum disorder; Autism Spectrum Disorder - metabolism; Brain - growth & development; Disease Models, Animal; Gene Expression - physiology; Male; Mice; Neurons - metabolism; Prefrontal cortex; Serotonin; Serotonin - metabolism; Serotonin Plasma Membrane Transport Proteins - genetics; Social; Social Behavior; Transcriptome; Social; Prefrontal cortex; Serotonin; Amygdala; Autism spectrum disorder; Transcriptome
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2020.135027

•A mutation in the serotonin transporter gene of mice affected expression of many genes compared to wildtype mice.•Genes were differentially expressed in response to a social stimulus compared to a non-social stimulus in the lateral and medial amygdala.•Fewer differences in gene expression due to social vs. non-social stimulus were observed in the prefrontal cortex.•Differentially expressed genes were associated with behavior, nervous system development, and neurotransmitter signaling. Multiple lines of evidence implicate the serotonin (5-HT) system in social function, including biomarker findings in autism spectrum disorder. In mice, knock-in of a rare Gly56Ala substitution in the serotonin transporter (SERT) causes elevated whole blood 5-HT levels, increased 5-HT clearance in the brain, and altered social and repetitive behavior. To further examine the molecular impact of this variant on social response, SERT Ala56 mutant mice and wildtype littermate controls were exposed to a social or non-social stimulus. We examined the differential activation of the prefrontal cortex, lateral amygdala, and medial amygdala, to social stimuli through RNA sequencing. Differentially expressed genes were enriched in axonal guidance signaling pathways, networks related to nervous system development and function, neurological and psychiatric disorders, and behavior. These identified pathways and networks may shed light on the molecular cascades underlying the impact of altered SERT function on social behavior.