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精神分裂症1基因、生物学与精神疾病

DISC1 genetics, biology and psychiatric illness.

作者信息

Thomson Pippa A, Malavasi Elise L V, Grünewald Ellen, Soares Dinesh C, Borkowska Malgorzata, Millar J Kirsty

机构信息

The Centre for Molecular Medicine at the Medical Research Council Institute of Genetics and Molecular Medicine, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.

出版信息

Front Biol (Beijing). 2013 Feb 1;8(1):1-31. doi: 10.1007/s11515-012-1254-7.

DOI:10.1007/s11515-012-1254-7
PMID:23550053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3580875/
Abstract

Psychiatric disorders are highly heritable, and in many individuals likely arise from the combined effects of genes and the environment. A substantial body of evidence points towards DISC1 being one of the genes that influence risk of schizophrenia, bipolar disorder and depression, and functional studies of DISC1 consequently have the potential to reveal much about the pathways that lead to major mental illness. Here, we review the evidence that DISC1 influences disease risk through effects upon multiple critical pathways in the developing and adult brain.

摘要

精神疾病具有高度遗传性,在许多个体中可能是由基因和环境的综合作用引起的。大量证据表明,DISC1是影响精神分裂症、双相情感障碍和抑郁症风险的基因之一,因此对DISC1的功能研究有可能揭示许多导致重大精神疾病的途径。在这里,我们综述了DISC1通过影响发育中和成人大脑中的多个关键途径来影响疾病风险的证据。

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DISC1 genetics, biology and psychiatric illness.精神分裂症1基因、生物学与精神疾病
Front Biol (Beijing). 2013 Feb 1;8(1):1-31. doi: 10.1007/s11515-012-1254-7.
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本文引用的文献

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Major depression: a role for hippocampal neurogenesis?重度抑郁症:海马体神经发生的作用?
Curr Top Behav Neurosci. 2013;14:153-79. doi: 10.1007/7854_2012_226.
2
Analysis of the DISC1 translocation partner (11q14.3) in genetic risk of schizophrenia.分析精神分裂症遗传风险中的 DISC1 易位伙伴(11q14.3)。
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Association of DISC1 variants with age of onset in a population-based sample of recurrent major depression.基于人群的复发性重度抑郁症样本中DISC1变体与发病年龄的关联。
Mol Psychiatry. 2013 Jul;18(7):745-7. doi: 10.1038/mp.2012.117. Epub 2012 Aug 7.
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Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis.DISC1 SNPs 对健康对照组和有精神病史患者大脑结构的影响。
Am J Med Genet B Neuropsychiatr Genet. 2012 Sep;159B(6):722-30. doi: 10.1002/ajmg.b.32076. Epub 2012 Jul 19.
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Brain-specific disruption of the eIF2α kinase PERK decreases ATF4 expression and impairs behavioral flexibility.脑特异性敲除 eIF2α 激酶 PERK 可降低 ATF4 表达并损害行为灵活性。
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Pathogenic disruption of DISC1-serine racemase binding elicits schizophrenia-like behavior via D-serine depletion.致病性 DISC1-丝氨酸消旋酶结合破坏通过 D-丝氨酸耗竭引起精神分裂症样行为。
Mol Psychiatry. 2013 May;18(5):557-67. doi: 10.1038/mp.2012.97. Epub 2012 Jul 17.
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Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia.网络辅助分析精神分裂症全基因组关联研究中的联合因果信号。
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The severity of mental disorders is linked to interaction among candidate genes.精神障碍的严重程度与候选基因的相互作用有关。
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Genetic architectures of psychiatric disorders: the emerging picture and its implications.精神障碍的遗传结构:新兴的图景及其影响。
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DISC1 and Striatal Volume: A Potential Risk Phenotype For mental Illness.DISC1与纹状体体积:一种潜在的精神疾病风险表型。
Front Psychiatry. 2012 Jun 19;3:57. doi: 10.3389/fpsyt.2012.00057. eCollection 2012.