A rare variant in <i>GPR156</i> associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice.
Miller BR., Gonzaga-Jauregui C., Brigatti KW., de Jong J., Breese RS., Ko SY., Puffenberger EG., Van Hout C., Young M., Luna VM., Staples J., First MB., Gregoire HJ., Dwork AJ., Pefanis E., McCarthy S., Brydges S., Rojas J., Ye B., Stahl E., Di Gioia SA., Hen R., Elwood K., Rosoklija G., Li D., Mellis S., Carey D., Croll SD., Overton JD., Macdonald LE., Economides AN., Shuldiner AR., Chuhma N., Rayport S., Amin N., Kushner SA., Alessandri-Haber N., Markx S., Strauss KA.
Major depressive disorder (MDD) is a leading cause of disability worldwide. Risk for MDD is heritable, and the genetic structure of founder populations enables investigation of rare susceptibility alleles with large effect. In an extended Old Order Mennonite family cohort, we identified a rare missense variant in GPR156 (c.1599G>T, p.Glu533Asp) associated with a two-fold increase in the relative risk of MDD. GPR156 is an orphan G protein-coupled receptor localized in the medial habenula, a region implicated in mood regulation. Insertion of a human sequence containing c.1599G>T into the murine Gpr156 locus induced medial habenula hyperactivity and abnormal stress-related behaviors. This work reveals a human variant that is associated with depression, implicates GPR156 as a target for mood regulation, and introduces informative murine models for investigating the pathophysiology and treatment of affective disorders.