TY - JOUR
T1 - TGFB-induced factor (TGIF)
T2 - A candidate gene for psychosis on chromosome 18p
AU - Chavarría-Siles, I.
AU - Walss-bass, Consuelo
AU - Quezada, P.
AU - Dassori, Albana M
AU - Contreras, S.
AU - Medina, R.
AU - Ramírez, M.
AU - Armas, R.
AU - Salazar, R.
AU - Leach, R. J.
AU - Raventos, H.
AU - Escamilla, M. A.
N1 - Funding Information:
This project was supported in part by NIH Research Grant # D43 TW06152 funded by the Fogarty International Center, The National Institute on Drug Abuse and the National Institute of Mental Health, and by the National Institutes of Health Grant R01-MH61884.
PY - 2007/11
Y1 - 2007/11
N2 - Schizophrenia (SC) and bipolar disorder (BP) share many clinical features, among them psychosis. We previously identified a putative gene locus for psychosis on chromosome 18p in a sample from the Central Valley of Costa Rica (CVCR) population. The present study replicated the association to a specific allele of microsatellite marker D18S63 on 18p11.3, using a newly collected sample from the CVCR. A combined analysis of both samples, plus additional subjects, showed that this specific allele on D18S63, which lies within an intron on the TGFB-induced factor (TGIF) gene, is strongly associated (P-value=0.0005) with psychosis. Eleven additional SNP markers, spanning five genes in the region, were analyzed in the combined sample from the CVCR. Only the four SNPs within the TGIF gene were in strong linkage disequilibrium with D18S63 (D′=1.00). A specific haplotype for all five markers within the TGIF gene showed evidence of association (P-value=0.011) to psychosis. A second, distinct haplotype, containing a newly identified nonsynonymous polymorphism in exon 5 of the TGIF gene, showed a nonsignificant trend towards association to psychosis (P-value=0.077). TGIF is involved in neurodevelopment, neuron survival and controls the expression of dopamine receptors. Altogether, our results point to the possible involvement of TGIF in the pathophysiology of psychotic disorders in the CVCR population.
AB - Schizophrenia (SC) and bipolar disorder (BP) share many clinical features, among them psychosis. We previously identified a putative gene locus for psychosis on chromosome 18p in a sample from the Central Valley of Costa Rica (CVCR) population. The present study replicated the association to a specific allele of microsatellite marker D18S63 on 18p11.3, using a newly collected sample from the CVCR. A combined analysis of both samples, plus additional subjects, showed that this specific allele on D18S63, which lies within an intron on the TGFB-induced factor (TGIF) gene, is strongly associated (P-value=0.0005) with psychosis. Eleven additional SNP markers, spanning five genes in the region, were analyzed in the combined sample from the CVCR. Only the four SNPs within the TGIF gene were in strong linkage disequilibrium with D18S63 (D′=1.00). A specific haplotype for all five markers within the TGIF gene showed evidence of association (P-value=0.011) to psychosis. A second, distinct haplotype, containing a newly identified nonsynonymous polymorphism in exon 5 of the TGIF gene, showed a nonsignificant trend towards association to psychosis (P-value=0.077). TGIF is involved in neurodevelopment, neuron survival and controls the expression of dopamine receptors. Altogether, our results point to the possible involvement of TGIF in the pathophysiology of psychotic disorders in the CVCR population.
KW - Bipolar disorder
KW - Central valley of Costa Rica
KW - Psychosis
KW - Schizophrenia
KW - TGIF
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U2 - 10.1038/sj.mp.4001997
DO - 10.1038/sj.mp.4001997
M3 - Article
C2 - 17440433
AN - SCOPUS:35548943080
SN - 1359-4184
VL - 12
SP - 1033
EP - 1041
JO - Molecular psychiatry
JF - Molecular psychiatry
IS - 11
ER -