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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >High-resolution chromosome ideogram representation of recognized genes for bipolar disorder
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High-resolution chromosome ideogram representation of recognized genes for bipolar disorder

机译:躁郁症公认基因的高分辨率染色体表意文字表示

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摘要

Bipolar disorder (BPD) is genetically heterogeneous with a growing list of BPD associated genes reported in recent years resulting from increased genetic testing using advanced genetic technology, expanded genomic data-bases, and better awareness of the disorder. We compiled a master list of recognized susceptibility and genes associated with BPD identified from peer-reviewed medical literature sources using PubMed and by searching online databases, such as OMIM. Searched keywords were related to bipolar disorder and genetics. Our compiled list consisted of 290 genes with gene names arranged in alphabetical order in tabular form with source documents and their chromosome location and gene symbols plotted on high-resolution human chromosome ideograms. The identified genes impacted a broad range of biological pathways and processes including cellular signaling pathways particularly cAMP and calcium (e.g., CACNA1C, CAMK2A, CAMK2D, ADCY1, ADCY2); glutamatergic (e.g., GRIK1, GRM3, GRM7), dopaminergic (e.g., DRD2, DRD4, COMT, MAOA) and serotonergic (e.g., HTR1A, HTR2A, HTR3B) neurotransmission; molecular transporters (e.g., SLC39A3, SLC6A3, SLC8A1); and neuronal growth (e.g., BDNF, IGFBPI, NRG1, NRG3). The increasing prevalence of BPD calls for better understanding of the genetic etiology of this disorder and associations between the observed BPD phenotype and genes. Visual representation of genes for bipolar disorder becomes a tool enabling clinical and laboratory geneticists, genetic counselors, and other health care providers and researchers easy access to the location and distribution of currently recognized BPD associated genes. Our study may also help inform diagnosis and advance treatment developments for those affected with this disorder and improve genetic counseling for families. (C) 2016 Elsevier B.V. All rights reserved.
机译:双相情感障碍(BPD)在遗传上是异质的,近年来报道了BPD相关基因的列表不断增加,这归因于使用先进的遗传技术进行的基因测试增加,基因组数据库的扩展以及对该疾病的更好的了解。我们使用PubMed并通过搜索在线数据库(例如OMIM),编制了一份公认的易感性和与BPD相关的基因的主列表,这些基因是从经过同行评审的医学文献来源中鉴定的。搜索到的关键词与躁郁症和遗传有关。我们编制的清单包括290个基因,这些基因的基因名称以字母顺序排列在表格中,并带有源文件,其染色体位置和基因符号绘制在高分辨率人类染色体表意文字上。鉴定出的基因影响了广泛的生物学途径和过程,包括细胞信号途径,特别是cAMP和钙(例如,CACNA1C,CAMK2A,CAMK2D,ADCY1,ADCY2);谷氨酸能(例如GRIK1,GRM3,GRM7),多巴胺能(例如DRD2,DRD4,COMT,MAOA)和血清素能(例如HTR1A,HTR2A,HTR3B)神经传递;分子转运蛋白(例如SLC39A3,SLC6A3,SLC8A1);和神经元生长(例如BDNF,IGFBPI,NRG1,NRG3)。 BPD患病率的提高要求人们更好地了解这种疾病的遗传病因,以及所观察到的BPD表型与基因之间的关联。视觉表达双相情感障碍的基因已成为一种工具,使临床和实验室遗传学家,遗传咨询师以及其他医疗保健提供者和研究人员可以轻松访问当前公认的BPD相关基因的位置和分布。我们的研究还可能有助于为患有这种疾病的人提供诊断信息并促进治疗的发展,并改善家庭的遗传咨询。 (C)2016 Elsevier B.V.保留所有权利。

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