Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit.

Détails

ID Serval
serval:BIB_265FA81F58C0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit.
Périodique
Proceedings of the National Academy of Sciences of the United States of America
Auteur⸱e⸱s
Gerber D.J., Hall D., Miyakawa T., Demars S., Gogos J.A., Karayiorgou M., Tonegawa S.
ISSN
0027-8424 (Print)
ISSN-L
0027-8424
Statut éditorial
Publié
Date de publication
2003
Volume
100
Numéro
15
Pages
8993-8998
Langue
anglais
Résumé
Schizophrenia is a severe psychiatric disorder characterized by a complex mode of inheritance. Forebrain-specific CNB knockout mice display a spectrum of behavioral abnormalities related to altered behaviors observed in schizophrenia patients. To examine whether calcineurin dysfunction is involved in schizophrenia etiology, we undertook studies of an initial subset of calcineurin-related genes, prioritizing ones that map to loci previously implicated in schizophrenia by linkage studies. Transmission disequilibrium studies in a large sample of affected families detected association of the PPP3CC gene, which encodes the calcineurin gamma catalytic subunit, with disease. Our results identify PPP3CC, located at 8p21.3, as a potential schizophrenia susceptibility gene and support the proposal that alterations in calcineurin signaling contribute to schizophrenia pathogenesis.
Mots-clé
Adult, Base Sequence, Calcineurin/chemistry, Calcineurin/genetics, Chromosome Mapping, Chromosomes, Human, Pair 8/genetics, DNA, Complementary/genetics, Genetic Variation, Haplotypes, Humans, Polymorphism, Genetic, Protein Subunits, Schizophrenia/etiology, Schizophrenia/genetics, Signal Transduction
Pubmed
Open Access
Oui
Création de la notice
27/02/2012 17:40
Dernière modification de la notice
20/08/2019 14:05
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