Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies.

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Title: Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies.
Authors: Schosser, A., Gaysina, D., Cohen-Woods, S., Chow, P. C., Martucci, L., Craddock, N., Farmer, A., Korszun, A., Gunasinghe, C., Gray, J., Jones, L., Tozzi, F., Perry, J., Muglia, P., Owen, M. J., Craig, I. W., McGuffin, P.
Source: Molecular Psychiatry. Aug2010, Vol. 15 Issue 8, p844-849. 6p. 3 Charts.
Subjects: Schizophrenia, Genes, Bipolar disorder, Mental depression, Mental illness, Genetic polymorphisms
Abstract: The gene known as Disrupted-in-Schizophrenia-1, DISC1, was originally discovered in a large family, in which it also co-segregated with bipolar affective disorder (BD) and with major depressive disorder (MDD). The TSNAX (Translin-associated factor X) gene, located immediately upstream of DISC1, has also been suggested as a candidate gene in relation to psychiatric illness, as one transcript resulting from intergenic splicing encodes a novel TSNAX–DISC1 fusion protein. We explored the TSNAX–DISC1 gene region for an association with BD and MDD in a sample of 1984 patients (1469 MDD, 515 BD) and 1376 ethnically matched controls. Eight single nucleotide polymorphisms (SNPs) within the TSNAX–DISC1 region (rs766288, rs3738401, rs2492367, rs6675281, rs12133766, rs1000731, rs7546310 and rs821597) were investigated using the SNPlex Genotyping System. We found a significant allelic and genotypic association of the TSNAX–DISC1 gene region with BD, whereas a haplotypic association was found for both BD and MDD. Therefore, our results suggest an association between the TSNAX–DISC1 region and both forms of affective disorders, and support the hypothesis that a portion of the genotypic overlap between schizophrenia and affective disorders is attributable to this gene. [ABSTRACT FROM AUTHOR]
Copyright of Molecular Psychiatry is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies.
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  Data: <searchLink fieldCode="AR" term="%22Schosser%2C+A%2E%22">Schosser, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Gaysina%2C+D%2E%22">Gaysina, D.</searchLink><br /><searchLink fieldCode="AR" term="%22Cohen-Woods%2C+S%2E%22">Cohen-Woods, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Chow%2C+P%2E+C%2E%22">Chow, P. C.</searchLink><br /><searchLink fieldCode="AR" term="%22Martucci%2C+L%2E%22">Martucci, L.</searchLink><br /><searchLink fieldCode="AR" term="%22Craddock%2C+N%2E%22">Craddock, N.</searchLink><br /><searchLink fieldCode="AR" term="%22Farmer%2C+A%2E%22">Farmer, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Korszun%2C+A%2E%22">Korszun, A.</searchLink><br /><searchLink fieldCode="AR" term="%22Gunasinghe%2C+C%2E%22">Gunasinghe, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Gray%2C+J%2E%22">Gray, J.</searchLink><br /><searchLink fieldCode="AR" term="%22Jones%2C+L%2E%22">Jones, L.</searchLink><br /><searchLink fieldCode="AR" term="%22Tozzi%2C+F%2E%22">Tozzi, F.</searchLink><br /><searchLink fieldCode="AR" term="%22Perry%2C+J%2E%22">Perry, J.</searchLink><br /><searchLink fieldCode="AR" term="%22Muglia%2C+P%2E%22">Muglia, P.</searchLink><br /><searchLink fieldCode="AR" term="%22Owen%2C+M%2E+J%2E%22">Owen, M. J.</searchLink><br /><searchLink fieldCode="AR" term="%22Craig%2C+I%2E+W%2E%22">Craig, I. W.</searchLink><br /><searchLink fieldCode="AR" term="%22McGuffin%2C+P%2E%22">McGuffin, P.</searchLink>
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  Data: <searchLink fieldCode="DE" term="%22Schizophrenia%22">Schizophrenia</searchLink><br /><searchLink fieldCode="DE" term="%22Genes%22">Genes</searchLink><br /><searchLink fieldCode="DE" term="%22Bipolar+disorder%22">Bipolar disorder</searchLink><br /><searchLink fieldCode="DE" term="%22Mental+depression%22">Mental depression</searchLink><br /><searchLink fieldCode="DE" term="%22Mental+illness%22">Mental illness</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+polymorphisms%22">Genetic polymorphisms</searchLink>
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  Data: The gene known as Disrupted-in-Schizophrenia-1, DISC1, was originally discovered in a large family, in which it also co-segregated with bipolar affective disorder (BD) and with major depressive disorder (MDD). The TSNAX (Translin-associated factor X) gene, located immediately upstream of DISC1, has also been suggested as a candidate gene in relation to psychiatric illness, as one transcript resulting from intergenic splicing encodes a novel TSNAX–DISC1 fusion protein. We explored the TSNAX–DISC1 gene region for an association with BD and MDD in a sample of 1984 patients (1469 MDD, 515 BD) and 1376 ethnically matched controls. Eight single nucleotide polymorphisms (SNPs) within the TSNAX–DISC1 region (rs766288, rs3738401, rs2492367, rs6675281, rs12133766, rs1000731, rs7546310 and rs821597) were investigated using the SNPlex Genotyping System. We found a significant allelic and genotypic association of the TSNAX–DISC1 gene region with BD, whereas a haplotypic association was found for both BD and MDD. Therefore, our results suggest an association between the TSNAX–DISC1 region and both forms of affective disorders, and support the hypothesis that a portion of the genotypic overlap between schizophrenia and affective disorders is attributable to this gene. [ABSTRACT FROM AUTHOR]
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  Data: <i>Copyright of Molecular Psychiatry is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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