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Malic enzyme 2 and susceptibility to psychosis and mania

dc.creatorDae Lee, Byung
dc.creatorWalss Bass, Consuelo
dc.creatorThompson, Peter M.
dc.creatorDassori, Albana Maria
dc.creatorMontero Vega, Ana Patricia
dc.creatorMedina, Rolando
dc.creatorContreras, Salvador A.
dc.creatorArmas, Regina
dc.creatorRamírez, Mercedez Ellis
dc.creatorPereira Castro, Mariana
dc.creatorSalazar Fonseca, Rodolfo
dc.creatorLeach, Robin Jean
dc.creatorQuezada, Paulina
dc.creatorRaventós Vorst, Henriette
dc.creatorEscamilla, Michael A.
dc.date.accessioned2024-12-10T16:57:29Z
dc.date.available2024-12-10T16:57:29Z
dc.date.issued2007-01-29
dc.description.abstractPrevious studies have identified a putative gene locus for both schizophrenia and bipolar disorder in the chromosome 18q21 region. To identify candidate genes associated with these disorders we completed fine mapping analyses (using microsatellite markers) in 152 families from the Central Valley of Costa Rica (CVCR) (376 total subjects, 151 with a history of psychosis, 97 with a history of mania). Microsatellite analyses showed evidence of association at two contiguous markers, both located at the same genetic distance and spanning approximately 11 known genes. In a corollary gene expression study, one of these genes, malic enzyme 2 (ME2), showed levels of gene expression 5.6-fold lower in anterior cingulate tissue from post-mortem bipolar brains. Subsequent analysis of individual SNPs in strong linkage disequilibrium with the ME2 gene revealed one SNP and one haplotype associated with the phenotype of psychosis in the CVCR sample. ME2 interacts directly with the malate shuttle system, which has been shown to be altered in schizophrenia and bipolar disorder, and has roles in neuronal synthesis of glutamate and gamma-amino butyric acid. The present study suggests that genetic variation in or near the ME2 gene is associated with both psychotic and manic disorders, including schizophrenia and bipolar disorder.
dc.description.procedenceUCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias Básicas::Centro de Investigación en Biología Celular y Molecular (CIBCM)
dc.description.procedenceUCR::Vicerrectoría de Docencia::Ciencias Básicas::Facultad de Ciencias::Escuela de Biología
dc.description.procedenceUCR::Vicerrectoría de Docencia::Salud::Facultad de Medicina::Escuela de Medicina
dc.description.sponsorshipInstituto Nacional de Salud/[R01-MH61884]/NIH/Estados Unidos
dc.description.sponsorshipInstituto Nacional de Salud/[K01 MH01453]/NIH/Estados Unidos
dc.description.sponsorshipBrain & Behavior Research Foundation/[]/BBRF/Estados Unidos
dc.description.sponsorshipHoward Hughes Medical Institute/[]/HHMI/Estados Unidos
dc.description.sponsorshipUniversity of Texas Health Science Center at San Antonio/[]/UTHSCSA/Estados Unidos
dc.description.sponsorshipInternational Center for Genetic Engineering and Biotechnology/[CRP/COS98-01]/ICGEB/Italia
dc.identifier.doihttps://doi.org/10.1016/j.psychres.2006.06.001
dc.identifier.issn0165-1781
dc.identifier.issn1872-7123
dc.identifier.urihttps://hdl.handle.net/10669/100235
dc.language.isoeng
dc.rightsacceso restringido
dc.sourcePsychiatry Research, 150(1), 1-11
dc.subjectMalic enzyme
dc.subjectBipolar disorder
dc.subjectSchizophrenia
dc.subjectCosta Rica
dc.subjectGenetics
dc.titleMalic enzyme 2 and susceptibility to psychosis and mania
dc.typeartículo original

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