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
  • [21] TETRASOMY OF THE SHORT ARMS OF THE (18P) CHROMOSOME - CYTOGENETICS, DISTURBANCES IN PHENOTYPE
    KULESHOV, NP
    ZALETAEV, DV
    LEVINA, LY
    DEMENTYEVA, GM
    ARBUZOV, SP
    TSITOLOGIYA I GENETIKA, 1985, 19 (06): : 452 - 456
  • [22] Evidence that a locus for familial high myopia maps to chromosome 18p
    Young, TL
    Ronan, SM
    Drahozal, LA
    Wildenberg, SC
    Alvear, AB
    Oetting, WS
    Atwood, LD
    Wilkin, DJ
    King, RA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) : 109 - 119
  • [23] Genetic analysis of three patients with dystonia and deletion in chromosome 18p
    Page, CE
    Klein, C
    Ozelius, LJ
    Gordon, MF
    LeWitt, PA
    Brin, MF
    NEUROLOGY, 1998, 50 (04) : A427 - A427
  • [24] Psychosis, leukodystrophy, and dysmorphology in a microarray-confirmed 18p monosomy case
    Drazinic, CM
    Pletcher, BA
    Zheng, H
    State, MW
    BIOLOGICAL PSYCHIATRY, 2006, 59 (08) : 81S - 82S
  • [25] Follow-up of adult males with chromosome 18p deletion
    de Ravel, TJL
    Thiry, P
    Fryns, JP
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2005, 48 (02) : 189 - 193
  • [26] The genotype and phenotype of chromosome 18p deletion syndrome Case series
    Jin, Qiujie
    Qiang, Rong
    Cai, Bo
    Wang, Xiaobin
    Cai, Na
    Zhen, Shuai
    Zhai, Wen
    MEDICINE, 2021, 100 (18) : E25777
  • [27] Assignment of the gene responsible for chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia to the short arm of chromosome 18 and examination of TGIF as a candidate gene.
    Tayeh, MK
    Majeed, HA
    Al-Masri, N
    Al-Rimawi, H
    Pelet, A
    Munnich, A
    Lyonnet, S
    El-Shanti, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 326 - 326
  • [28] Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy
    Kocaaga, Ayca
    Yimenicioglu, Sevgi
    GLOBAL MEDICAL GENETICS, 2022, 09 (02): : 179 - 181
  • [29] TETRASOMY OF SHORT ARMS OF CHROMOSOME-18, WITH A 47,XX,I(18P) KARYOTYPE
    MUTCHINICK, O
    RUZ, E
    SALAMANCA, F
    ARMENDARES, S
    REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, 1978, 30 (01): : 101 - 101
  • [30] High-density radiation hybrid map of human chromosome 18 and contig of 18p
    Giacalone, J
    Li, X
    Lehrach, H
    Francke, U
    GENOMICS, 1996, 37 (01) : 9 - 18