Mouse model of the human serotonin transporter-linked polymorphic region

• Published in: Mammalian genome 2019-12, Vol.30 (11-12), p.319-328
• Main Authors: Piszczek, Lukasz, Memoli, Simone, Raggioli, Angelo, Viosca, José, Rientjes, Jeanette, Hublitz, Philip, Czaban, Weronika, Wyrzykowska, Anna, Gross, Cornelius
• Format: Article
• Language: English
• Subjects: Animal Genetics and Genomics; Anxiety; Biomedical and Life Sciences; Cell Biology; Gene expression; Gene polymorphism; Genetic diversity; Genetic factors; Homeostasis; Human Genetics; Life Sciences; Monoamines; Mood; Neurosis; Polymorphism; Risk factors; Serotonin; Serotonin transporter; Transgenes
• ISSN: 0938-8990; 1432-1777
• DOI: 10.1007/s00335-019-09815-2

Genetic factors play a significant role in risk for mood and anxiety disorders. Polymorphisms in genes that regulate the brain monoamine systems, such as catabolic enzymes and transporters, are attractive candidates for being risk factors for emotional disorders given the weight of evidence implicating monoamines involvement in these conditions. Several common genetic variants have been identified in the human serotonin transporter (5-HTT) gene, including a repetitive sequence located in the promoter region of the locus called the serotonin transporter-linked polymorphic region (5-HTT-LPR). This polymorphism has been associated with a number of mental traits in both humans and primates, including depression, neuroticism, and harm avoidance. Some, but not all, studies found a link between the polymorphism and 5-HTT levels, leaving open the question of whether the polymorphism affects risk for mental traits via changes in 5-HTT expression. To investigate the impact of the polymorphism on gene expression, serotonin homeostasis, and behavioral traits, we set out to develop a mouse model of the human 5-HTT-LPR. Here we describe the creation and characterization of a set of mouse lines with single-copy human transgenes carrying the short and long 5-HTT-LPR variants. Although we were not able to detect differences in expression between the short and long variants, we encountered several technical issues concerning the design of our humanized mice that are likely to have influenced our findings. Our study serves as a cautionary note for future studies aimed at studying human transgene regulation in the context of the living mouse.