Abstract
The importance of YWHAE gene polymorphisms (rs1532976, rs3752826, and rs9393) in the development of suicidal behavior has been studied in ethnic groups of Russians and Tatars from the Republic of Bashkortostan. It was revealed that the carriers of the YWHAE*C allele of rs3752826 polymorphism of the YWHAE gene have increased the risk of suicidal behavior (OR = 1.91), regardless of their ethnicity. In addition, the YWHAE*T allele of rs9393 polymorphism (OR = 2.21), YWHAE*T/*T genotype (OR = 2.73), and YWHAE*T allele (OR = 1.52) of the rs1532976 polymorphism, as well as the YWHAE*A*T haplotype of rs1532976 and rs9393 polymorphisms (OR = 1.54) represent genetic markers of the risk of suicidal behavior in the sample of subjects of Russian ethnicity.
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Sluchanko, N.N., Gusev, N.B., The 14-3-3 Proteins and the Cytoskeleton Regulation, Usp. Boil. Khim., 2010, vol. 50, pp. 69–116.
Colson, N., Dodd, P., and Lewohl, J., Differential Expression of 14-3-3 Isoforms in Human Alcoholic Brain, Alcohol Clin. Exp. Res., 2011, vol. 35, no. 6, pp. 1041–1049.
Morrison, D., The 14-3-3 Proteins: Integrators of Diverse Signaling Cues That Impact Cell Fate and Cancer Development, Trends Cell Biol., 2009, vol. 19, pp. 16–23.
Boston, P., Jackson, P., Kynoch, P., and Thompson, R., Purification, Properties, and Immunohistochemical Localization of Human Brain 14-3-3 Protein, J. Neurochem., 1982, vol. 38, pp. 1466–1474.
Muslin, A., Tanner, J., Allen, P., and Shaw, A., Interaction of 14-3-3 with Signaling Proteins Is Mediated by the Recognition of Phosphoserine, Cell, 1996, vol. 84, pp. 889–897.
Berg, D., Holzmann, C., and Riess, O., 14-3-3 Proteins in the Nervous System, Nat. Neurosci., 2003, vol. 4, pp. 752–762.
Di Fede, G., Giaccone, G., Limido, L., et al., The Epsilon Isoform of 14-3-3 Protein Is a Component of the Prion Protein Amyloid Deposits of Gerstmann-Strussler-Scheinker Disease, J. Neuropathol. Exp. Neurol., 2007, vol. 66, no. 2, pp. 124–130.
Mackie, S. and Aitken, A., Novel Brain 14-3-3 Interacting Proteins Involved in Neurodegenerative Disease, FEBS J., 2005, vol. 272, no. 16, pp. 4202–4210.
Ikeda, M., Hikita, T., Taya, S., et al., Identification of YWHAE, a Gene Encoding 14-3-3 Epsilon, as a Possible Susceptibility Gene for Schizophrenia, Hum. Mol. Genet., 2008, vol. 17, no. 20, pp. 3212–3222.
Yanagi, M., Shirakawa, O., Kitamura, N., et al., Association of 14-3-3 Gene Haplotype with Completed Suicide in Japanese, J. Hum. Genet., 2005, vol. 50, pp. 210–216.
Ichimura, T., Isobe, T., Okuyama, T., et al., Brain 14-3-3 Protein Is an Activator Protein That Activates Tryptophan 5-Monooxygenase and Tyrosine 3-Monooxygenase in the Presence of Ca2+ Calmodulin-Dependent Protein Kinase II, FEBS Lett., 1987, vol. 219, pp. 79–82.
Ichimura, T., Isobe, T., Okuyama, T., et al., Molecular Cloning of cDNA Coding for Brain-Specific 14-3-3 Protein, a Protein Kinase-Dependent Activator of Tyrosine and Tryptophan Hydroxylases, Proc. Natl. Acad. Sci. U.S.A., 1988, vol. 85, pp. 7084–7088.
Aitken, A., Functional Specificity in 14-3-3 Isoform Interactions through Dimer Formation and Phosphorylation: Chromosome Location of Mammalian Isoforms and Variants, Plant Mol. Biol., 2002, vol. 50, pp. 993–1010.
Leal, M., Calcagno, D., Demachki, S., et al., Clinical Implication of 14-3-3 Epsilon Expression in Gastric Cancer, World J. Gastroenterol., 2012, vol. 18, no. 13, pp. 1531–1537.
Fountoulakis, M., Cairns, N., and Lubec, G., Increased Levels of 14-3-3 Gamma and Epsilon Proteins in Brain of Patients with Alzheimer’s Disease and Down Syndrome, J. Neur. Transm., 1999, vol. 57, suppl., pp. 323–35.
Sugimori, K., Kobayashi, K., Kitamura, T., et al., 14-3-3 Protein Beta Isoform Is Associated with 3-Repeat Tau Neurofibrillary Tangles in Alzheimer’s Disease, Psychiatry Clin. Neurosci., 2007, vol. 61, pp. 159–167.
Nagamani, S., Zhang, F., Shchelochkov, O., et al., Microdeletions Including YWHAE in the Miller-Dieker Syndrome Region on Chromosome 17p13.3 Result in Facial Dysmorphisms, Growth Restriction, and Cognitive Impairment, J. Med. Genet., 2009, vol. 46, pp. 825–833.
Toyo-oka, K., Shionoya, A., Gambello, M., et al., 14-3-3 Epsilon Is Important for Neuronal Migration by Binding to NUDEL: A Molecular Explanation for Miller-Dieker Syndrome, Nat. Genet., 2003, vol. 34, pp. 274–285.
Sánchez-Valle, R., Saiz, A., and Graus, F., 14-3-3 Protein Isoforms and Atypical Patterns of the 14-3-3 Assay in the Diagnosis of Creutzfeldt-Jakob Disease, Neurosci. Lett., 2002, vol. 320, nos. 1–2, pp. 69–72.
Cumbler, E., Furfari, K., and Guerrasio, J., Creutzfeldt-Jacob Disease Presenting as Severe Depression: A Case Report, Cases J., 2009, vol. 2, p. 122.
Wong, A.H., Likhodi, O., and Trakalo, J., Genetic and Post-Mortem mRNA Analysis of the 14-3-3 Genes That Encode Phosphoserine/Threonine-Binding Regulatory Proteins in Schizophrenia and Bipolar Disorder, Schizophr. Res., 2005, vol. 78, nos. 2–3, pp. 137–146.
Grover, D., Verma, R., Goes, F., et al., Family-Based Association of YWHAH in Psychotic Bipolar Disorder, Am. J. Med. Genet., 2009, vol. 150B, pp. 977–983.
Jacobs, B., Praag, H., and Gage, F., Adult Brain Neurogenesis and Psychiatry: A Novel Theory of Depression, Mol. Psychiatry, 2000, vol. 5, pp. 262–269.
Middleton, F., Peng, L., Lewis, D., et al., Altered Expression of 14-3-3 Genes in the Prefrontal Cortex of Subjects with Schizophrenia, Neuropsychopharmacology, 2005, vol. 30, no. 5, pp. 974–983.
Souza, D., Gattaz, W., Schmitt, A., et al., Prefrontal Cortex Shotgun Proteome Analysis Reveals Altered Calcium Homeostasis and Immune System Imbalance in Schizophrenia, Eur. Arch. Psychiatry Clin. Neurosci., 2009, vol. 259, no. 3, pp. 151–163.
Jia, Y., Yu, X., Zhang, B., et al., An Association Study between Polymorphisms in Three Genes of 14-3-3 (Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein) Family and Paranoid Schizophrenia in Northern Chinese Population, Eur. Psychiatry, 2004, vol. 19, no. 6, pp. 377–379.
Wong, A., Macciardi, F., Klempan, T., et al., Identification of Candidate Genes for Psychosis in Rat Models, and Possible Association between Schizophrenia and the 14-3-3g Gene, Mol. Psychiatry, 2003, vol. 8, pp. 156–166.
Baum, A., Akula, N., Cabanero, M., et al., A Genome-Wide Association Study Implicates Diacylglycerol Kinase Eta (DGKH) and Several Other Genes in the Etiology of Bipolar Disorder, Mol. Psychiatry, 2008, vol. 13, no. 2, pp. 197–207.
Sekiguchi, H., Iritani, S., Habuchi, C., et al., Impairment of the Tyrosine Hydroxylase Neuronal Network in the Orbitofrontal Cortex of a Genetically Modified Mouse Model of Schizophrenia, Brain Res., 2011, vol. 1392, pp. 47–53.
Mathew, C., The Isolation of High Molecular Weight Eukaryotic DNA, Methods Mol. Biol., 1985, vol. 2, pp. 31–34.
Schlesselman, J., Case-Control Studies: Design, Conduct, Analysis, New York: Oxford University Press, 1982.
Barrett, J., Fry, B., Maller, J., and Daly, M., Haploview: Analysis and Visualization of LD and Haplotype Maps, Bioinformatics, 2005, vol. 21, no. 2, pp. 263–265.
Chubb, J., Bradshaw, N., Soares, D., et al., The DISC Locus in Psychiatric Illness, Mol. Psychiatry, 2008, vol. 13, pp. 36–64.
Liu, J., Zhou, G., Ji, W., et al., No Association of the YWHAE Gene with Schizophrenia, Major Depressive Disorder or Bipolar Disorder in the Han Chinese Population, Behav. Genet., 2011, vol. 41, pp. 557–564.
Brezun, J. and Daszuta, A., Depletion in Serotonin Decreases Neurogenesis in the Dentate Gyrus and the Subventricular Zone of Adult Rats, Neuroscience, 1999, vol. 89, pp. 999–1002.
Nanavati, D., Austin, D., and Catapano, L., The Effects of Chronic Treatment with Mood Stabilizers on the Rat Hippocampal Postsynaptic Density Proteome, Neurochemistry, 2011, vol. 119, no. 3, pp. 617–629.
Baldessarini, R., Tondo, L., and Hennen, J., Treating the Suicidal Patient with Bipolar Disorder: Reducing Suicide Risk with Lithium, Ann. N.Y. Acad. Sci., 2001, vol. 932, pp. 24–38.
Goodwin, F., Fireman, B., Simon, G., et al., Suicide Risk in Bipolar Disorder during Treatment with Lithium and Divalproex, JAMA, 2003, vol. 17, no. 290, pp. 1467–1473.
Kim, J., Chang, M., Yu, I., et al., Lithium Selectively Increases Neuronal Differentiation of Hippocampal Neural Progenitor Cells both in vitro and in vivo, J. Neurochem., 2004, vol. 89, pp. 324–336.
Meltzer, H., Alphs, L., Green, A., et al., International Suicide Prevention Trial Study Group: Clozapine Treatment for Suicidality in Schizophrenia: International Suicide Prevention Trial (Inter-SePT), Arch. Gen. Psychiatry, 2003, vol. 60, pp. 82–91.
Halim, N., Weickert, C., McClintock, B., et al., Effects of Chronic Haloperidol and Clozapine Treatment on Neurogenesis in the Adult Rat Hippocampus, Neuropsychopharmacology, 2004, vol. 29, pp. 1063–1069.
Choi, M., Hwang, S., and Park, G., Effect of Fluoxetine on the Expression of Tryptophan Hydroxylase and 14-3-3 Protein in the Dorsal Raphe Nucleus and Hippocampus of Rat, J. Chem. Neuroanat., 2012, vol. 43, no. 2, pp. 96–102.
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Original Russian Text © Z.L. Khalilova, A.G. Zainullina, A. R. Valiullina, G.G. Zakharova, R.G. Valinurov, E.K. Khusnutdinova, 2013, published in Genetika, 2013, Vol. 49, No. 6, pp. 767–772.
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Khalilova, Z.L., Zainullina, A.G., Valiullina, A.R. et al. Association of YWHAE gene polymorphism with suicidal behavior. Russ J Genet 49, 667–672 (2013). https://doi.org/10.1134/S1022795413030095
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DOI: https://doi.org/10.1134/S1022795413030095