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Published Online: 1 May 2010

Genetic Sensitivity to the Environment: The Case of the Serotonin Transporter Gene and Its Implications for Studying Complex Diseases and Traits

Abstract

Abstract

Evidence of marked variability in response among people exposed to the same environmental risk implies that individual differences in genetic susceptibility might be at work. The study of such Gene-by-Environment (GxE) interactions has gained momentum. In this article, the authors review research about one of the most extensive areas of inquiry: variation in the promoter region of the serotonin transporter gene (SLC6A4; also known as 5-HTT) and its contribution to stress sensitivity. Research in this area has both advanced basic science and generated broader lessons for studying complex diseases and traits. The authors evaluate four lines of evidence about the 5-HTT stress-sensitivity hypothesis: 1) observational studies about the serotonin transporter linked polymorphic region (5-HTTLPR), stress sensitivity, and depression in humans; 2) experimental neuroscience studies about the 5-HTTLPR and biological phenotypes relevant to the human stress response; 3) studies of 5-HTT variation and stress sensitivity in nonhuman primates; and 4) studies of stress sensitivity and genetically engineered 5-HTT mutations in rodents. The authors then dispel some misconceptions and offer recommendations for GxE research. The authors discuss how GxE interaction hypotheses can be tested with large and small samples, how GxE research can be carried out before as well as after replicated gene discovery, the uses of GxE research as a tool for gene discovery, the importance of construct validation in evaluating GxE research, and the contribution of GxE research to the public understanding of genetic science.

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Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 509 - 527
PubMed: 20231323

History

Received: 12 October 2008
Accepted: 5 January 2010
Published online: 1 May 2010
Published in print: May 2010

Authors

Affiliations

Rudolf Uher, Ph.D., M.R.C.Psych.
Terrie E. Moffitt, Ph.D.

Notes

Received Oct. 12, 2009; revisions received Dec. 18 and Dec. 29, 2009; accepted Jan. 5, 2010. From the Departments of Psychology & Neuroscience, Psychiatry & Behavioral Sciences, and Institute for Genome Sciences and Policy, Duke University; the Social, Genetic, and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London; and the Section on Behavioral Science and Genetics, National Institute on Alcohol Abuse and Alcoholism, NIH. Address correspondence and reprint requests to Dr. Caspi, Duke University, 2020 West Main Street, Suite 201, Box 104410, Durham, NC 27708; [email protected] (e-mail).

Competing Interests

Drs. Caspi and Moffitt, through the Wisconsin Alumni Research Foundation, have applied for a patent entitled "Method for Assessing a Behavioral Disposition" (U.S. Patent Office serial number 10/889,450). The remaining authors report no financial relationships with commercial interests.

Funding Information

Supported by grants from the U.K. Medical Research Council (G0100527, G0601483), National Institute on Aging (AG032282), NIMH (MH077874, MH072837), NICHD (HD061298), and Intramural Research Program of the National Institute on Alcohol Abuse and Alcoholism. Avshalom Caspi is a Royal Society-Wolfson Merit Award holder.

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