(2016) Sekar, Aswin; Rosen, Allison; de Rivera, Heather; Bell, Avery; Hammond, Timothy; Kamitaki, Nolan; Tooley, Katherine; Presumey, Jessy; Baum, Matt; Van Doren, Vanessa; Genovese, Giulio; Rose, Samuel A.; Handsaker, Robert; Daly, Mark; Carroll, Michael C.; Stevens, Beth; McCarroll, Steven
Schizophrenia is a heritable brain illness with unknown pathogenic mechanisms. Schizophrenia’s strongest genetic association at a population level involves variation in the Major Histocompatibility Complex (MHC) locus, but the genes and molecular mechanisms accounting for this have been challenging to recognize. We show here that schizophrenia’s association with the MHC locus arises in substantial part from many structurally diverse alleles of the complement component 4 (C4) genes. We found that these alleles promoted widely varying levels of C4A and C4B expression and associated with schizophrenia in proportion to their tendency to promote greater expression of C4A in the brain. Human C4 protein localized at neuronal synapses, dendrites, axons, and cell bodies. In mice, C4 mediated synapse elimination during postnatal development. These results implicate excessive complement activity in the development of schizophrenia and may help explain the reduced numbers of synapses in the brains of individuals affected with schizophrenia.
