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The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression

Authors :
Gerome Breen
Daria Salyakina
Marianne B. Müller
Florian Holsboer
Martin A. Kohli
Henning Tiemeier
Thomas Bettecken
Mathias V. Schmidt
Marcus Ising
Kerry J. Ressler
Marcella Rietschel
Karin Hek
Bertram Müller-Myhsok
Elisabeth B. Binder
Angela Heck
Stephan Ripke
Andreas Menke
Cornelia M. van Duijn
Johannes Schramm
Markus M. Nöthen
Albert J. Becker
Michael Alexander
Johannes M. Hennings
Stefan Schreiber
Cathryn M. Lewis
Wolfgang Maier
Michael Specht
Darina Czamara
Bekh Bradley
Philipp G. Saemann
Susanne Lucae
Christiane Wolf
Ian W. Craig
Sven Cichon
Manfred Uhr
Michael Czisch
Ayse Demirkan
Albert Hofman
D. Hoehn
Epidemiology
Psychiatry
Child and Adolescent Psychiatry / Psychology
Source :
Neuron, 70(2), 252-265. Cell Press
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

Major depression (MD) is one of the most prevalent psychiatric disorders and a leading cause of loss in work productivity. A combination of genetic and environmental risk factors likely contributes to MD. We present data from a genome-wide association study revealing a neuron-specific neutral amino acid transporter (SLC6A15) as a novel susceptibility gene for MD. Risk allele carrier status in humans and chronic stress in mice were associated with a downregulation of the expression of this gene in the hippocampus, a brain region implicated in the pathophysiology of MD. The same polymorphisms also showed associations with alterations in hippocampal volume and neuronal integrity. Thus, decreased SLC6A15 expression, due to genetic or environmental factors might alter neuronal circuits related to the susceptibility for MD. Our convergent data from human genetics, expression studies, brain imaging and animal models suggest a novel pathophysiological mechanism for MD that may be accessible to drug targeting.

Details

ISSN :
08966273
Volume :
70
Database :
OpenAIRE
Journal :
Neuron
Accession number :
edsair.doi.dedup.....f820c873436850654d195650f780c12d
Full Text :
https://doi.org/10.1016/j.neuron.2011.04.005