TGFB-induced factor (TGIF):: a candidate gene for psychosis on chromosome 18p

被引:17
|
作者
Chavarria-Siles, I.
Walss-Bass, C.
Quezada, P.
Dassori, A.
Contreras, S.
Medina, R.
Ramirez, M.
Armas, R.
Salazar, R.
Leach, Rj
Raventos, H.
Escamilla, M. A.
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Psychiat, Psychiat Genet Res Ctr, San Antonio, TX 78229 USA
[2] Univ Costa Rica, Ctr Invest Biol Cellular & Mol, San Jose, Costa Rica
[3] Univ Calif San Francisco, Langley Porter Psychiat Inst, San Francisco, CA 94143 USA
[4] Univ Texas Hlth Ctr, Dept Cell & Struct Biol, San Antonio, TX USA
关键词
TGIF; psychosis; schizophrenia; bipolar disorder; central valley of Costa Rica;
D O I
10.1038/sj.mp.4001997
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1033 / 1041
页数:9
相关论文
共 50 条
  • [41] Characterisation of complex chromosome 18p rearrangements in two syndromic patients with immunological deficits
    Recalcati, Maria Paola
    Valtorta, Emanuele
    Romitti, Lorenza
    Giardino, Daniela
    Manfredini, Emanuela
    Vaccari, Roberto
    Larizza, Lidia
    Finelli, Palma
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2010, 53 (04) : 186 - 191
  • [42] Breakpoint mapping using microarrays and FISH in an 18p monosomy case with psychosis, leukodystrophy, and dysmorphology
    Drazinic, C. M.
    Pletcher, B. A.
    Zheng, H.
    State, M. W.
    BEHAVIOR GENETICS, 2006, 36 (06) : 963 - 963
  • [43] Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature
    Eleonora Marchina
    Michela Forti
    Mariella Tonelli
    Stefania Maccarini
    Francesca Malvestiti
    Chiara Piantoni
    Elena Filippini
    Elisa Fazzi
    Giuseppe Borsani
    Molecular Cytogenetics, 14
  • [44] Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature
    Marchina, Eleonora
    Forti, Michela
    Tonelli, Mariella
    Maccarini, Stefania
    Malvestiti, Francesca
    Piantoni, Chiara
    Filippini, Elena
    Fazzi, Elisa
    Borsani, Giuseppe
    MOLECULAR CYTOGENETICS, 2021, 14 (01)
  • [45] Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18
    Prabhakara, K
    Wyandt, HE
    Huang, XL
    Prasad, KS
    Ramadevi, AR
    ANNALES DE GENETIQUE, 2004, 47 (03): : 297 - 303
  • [46] Trisomy 18p Caused by a Supernumerary Marker With a Chromosome 13/21 Centromere: A Possible Recurrent Chromosome Aberration
    Plaja, Alberto
    Lloveras, Elisabet
    Martinez-Bouzas, Cristina
    Barrena, Beatriz
    Del Campo, Miguel
    Fernandez, Asuncion
    Herrero, Marta
    Barranco, Laura
    Palau, Nuria
    Asuncion Lopez-Ariztegui, M.
    Catala, Vicenc
    Tejada, Maria-Isabel
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161 (09) : 2363 - 2368
  • [47] Familial 4;18 chromosome translocation resulting in trisomy 4p and monosomy 18p: affected individuals with discordant phenotype
    Berman, Deborah R.
    Couyoumjian, Carrie A.
    Treadwell, Marjorie C.
    Barr, Mason, Jr.
    PRENATAL DIAGNOSIS, 2009, 29 (05) : 538 - 540
  • [48] A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype
    Banker, Deepa
    Mungala, Bhavdeep
    Parekh, Zankhana
    Ganatra, Shachi
    Maheshwari, Vimal
    Raj, Yashica
    Patel, Utsav
    Patel, Digant
    Chamar, Kishan
    Solanki, Vasu
    CASE REPORTS IN PEDIATRICS, 2023, 2023
  • [49] Sequence variants in the transforming growth β-induced factor (TGIF) gene are not associated with high myopia
    Scavello, GS
    Paluru, PC
    Ganter, WR
    Young, TL
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 (07) : 2091 - 2097
  • [50] MAP kinase pathway:: The link between neuregulin (NRG1) and TGF-β induced factor (TGIF), two candidate genes for psychosis in the Costa Rican population
    Chavarria-Siles, I.
    Escamilla, M.
    Raventos, H.
    Walss-Bass, C.
    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2008, 11 : 269 - 269