• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

与精神分裂症和双相情感障碍相关的基因在发育过程中的动态表达。

Dynamic expression of genes associated with schizophrenia and bipolar disorder across development.

机构信息

Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK.

MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.

出版信息

Transl Psychiatry. 2019 Feb 4;9(1):74. doi: 10.1038/s41398-019-0405-x.

DOI:10.1038/s41398-019-0405-x
PMID:30718481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6362023/
Abstract

Common genetic variation contributes a substantial proportion of risk for both schizophrenia and bipolar disorder. Furthermore, there is evidence of significant, but not complete, overlap in genetic risk between the two disorders. It has been hypothesised that genetic variants conferring risk for these disorders do so by influencing brain development, leading to the later emergence of symptoms. The comparative profile of risk gene expression for schizophrenia and bipolar disorder across development over different brain regions however remains unclear. Using genotypes derived from genome-wide associations studies of the largest available cohorts of patients and control subjects, we investigated whether genes enriched for schizophrenia and bipolar disorder association show a bias for expression across any of 13 developmental stages in prefrontal cortical and subcortical brain regions. We show that genetic association with schizophrenia is positively correlated with expression in the prefrontal cortex during early midfetal development and early infancy, and negatively correlated with expression during late childhood, which stabilises in adolescence. In contrast, risk-associated genes for bipolar disorder did not exhibit a bias towards expression at any prenatal stage, although the pattern of postnatal expression was similar to that of schizophrenia. These results highlight the dynamic expression of genes harbouring risk for schizophrenia and bipolar disorder across prefrontal cortex development and support the hypothesis that prenatal neurodevelopmental events are more strongly associated with schizophrenia than bipolar disorder.

摘要

常见的遗传变异对精神分裂症和双相情感障碍都有很大的影响。此外,有证据表明,这两种疾病之间存在显著但不完全的遗传风险重叠。有人假设,导致这些疾病风险的遗传变异是通过影响大脑发育,导致后来出现症状。然而,精神分裂症和双相情感障碍的风险基因表达在不同大脑区域的发育过程中的比较情况尚不清楚。我们利用来自最大的患者和对照组全基因组关联研究的基因型,研究了在 13 个发育阶段中,是否有与精神分裂症和双相情感障碍相关的基因富集,表现出在额皮质和皮质下脑区任何一个阶段的表达偏好。结果表明,与精神分裂症相关的遗传关联与早期中胎儿发育和婴儿早期的前额叶皮层表达呈正相关,与儿童晚期的表达呈负相关,到青春期趋于稳定。相比之下,双相情感障碍的风险相关基因在任何产前阶段都没有表现出表达偏好,但出生后的表达模式与精神分裂症相似。这些结果强调了携带精神分裂症和双相情感障碍风险的基因在额皮质发育过程中的动态表达,并支持了这样一种假设,即产前神经发育事件与精神分裂症的相关性强于双相情感障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/fc1a4fd881cb/41398_2019_405_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/e72de128ccb9/41398_2019_405_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/d14ee887a0f2/41398_2019_405_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/fc1a4fd881cb/41398_2019_405_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/e72de128ccb9/41398_2019_405_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/d14ee887a0f2/41398_2019_405_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb9f/6362023/fc1a4fd881cb/41398_2019_405_Fig3_HTML.jpg

相似文献

1
Dynamic expression of genes associated with schizophrenia and bipolar disorder across development.与精神分裂症和双相情感障碍相关的基因在发育过程中的动态表达。
Transl Psychiatry. 2019 Feb 4;9(1):74. doi: 10.1038/s41398-019-0405-x.
2
DEGS2 polymorphism associated with cognition in schizophrenia is associated with gene expression in brain.与精神分裂症认知相关的DEGS2基因多态性与大脑中的基因表达有关。
Transl Psychiatry. 2015 Apr 14;5(4):e550. doi: 10.1038/tp.2015.45.
3
Expression of ZNF804A in human brain and alterations in schizophrenia, bipolar disorder, and major depressive disorder: a novel transcript fetally regulated by the psychosis risk variant rs1344706.锌指蛋白 804A 在人脑组织中的表达及其在精神分裂症、双相情感障碍和重性抑郁障碍中的变化:由精神分裂症风险变异 rs1344706 调控的新型转录本在胎儿期表达。
JAMA Psychiatry. 2014 Oct;71(10):1112-20. doi: 10.1001/jamapsychiatry.2014.1079.
4
Developmental Profile of Psychiatric Risk Associated With Voltage-Gated Cation Channel Activity.电压门控阳离子通道活性相关的精神风险的发育概况。
Biol Psychiatry. 2021 Sep 15;90(6):399-408. doi: 10.1016/j.biopsych.2021.03.009. Epub 2021 Mar 13.
5
Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia.皮质组织的转录组分析揭示了自闭症和精神分裂症中下调基因的共享集。
Transl Psychiatry. 2016 May 24;6(5):e817. doi: 10.1038/tp.2016.87.
6
Temporal, Diagnostic, and Tissue-Specific Regulation of NRG3 Isoform Expression in Human Brain Development and Affective Disorders.人脑中NRG3亚型表达在脑发育和情感障碍中的时间、诊断及组织特异性调控
Am J Psychiatry. 2017 Mar 1;174(3):256-265. doi: 10.1176/appi.ajp.2016.16060721. Epub 2016 Oct 24.
7
A Multilevel Functional Study of a At-Risk Variant for Bipolar Disorder and Schizophrenia.双相情感障碍和精神分裂症风险变异体的多层次功能研究。
J Neurosci. 2017 Oct 25;37(43):10389-10397. doi: 10.1523/JNEUROSCI.1040-17.2017. Epub 2017 Oct 2.
8
Postmortem transcriptional profiling reveals widespread increase in inflammation in schizophrenia: a comparison of prefrontal cortex, striatum, and hippocampus among matched tetrads of controls with subjects diagnosed with schizophrenia, bipolar or major depressive disorder.尸检后转录谱分析显示精神分裂症中炎症广泛增加:在与被诊断为精神分裂症、双相或重度抑郁障碍的患者相匹配的四联体对照中,比较前额叶皮层、纹状体和海马。
Transl Psychiatry. 2019 May 23;9(1):151. doi: 10.1038/s41398-019-0492-8.
9
No association of Disrupted-in-Schizophrenia-1 variation with prefrontal function in patients with schizophrenia and bipolar disorder.精神分裂症 1 号基因缺失与精神分裂症和双相情感障碍患者前额叶功能无关联。
Genes Brain Behav. 2011 Apr;10(3):276-85. doi: 10.1111/j.1601-183X.2010.00665.x. Epub 2010 Dec 16.
10
CHRNA7 and CHRFAM7A mRNAs: co-localized and their expression levels altered in the postmortem dorsolateral prefrontal cortex in major psychiatric disorders.CHRNA7 和 CHRFAM7A mRNAs:在主要精神疾病的死后背外侧前额叶皮层中共定位,其表达水平改变。
Am J Psychiatry. 2015 Nov 1;172(11):1122-30. doi: 10.1176/appi.ajp.2015.14080978. Epub 2015 Jul 24.

引用本文的文献

1
Importin α4 deficiency induces psychiatric disorder-related behavioral deficits and neuroinflammation in mice.Importin α4 缺乏症可导致小鼠出现与精神疾病相关的行为缺陷和神经炎症。
Transl Psychiatry. 2024 Oct 8;14(1):426. doi: 10.1038/s41398-024-03138-w.
2
Sex-dependent effects of Setd1a haploinsufficiency on development and adult behaviour.Setd1a 杂合不足对发育和成年行为的性别依赖性影响。
PLoS One. 2024 Aug 14;19(8):e0298717. doi: 10.1371/journal.pone.0298717. eCollection 2024.
3
The contribution of silencer variants to human diseases.

本文引用的文献

1
Genome-wide association study identifies 30 loci associated with bipolar disorder.全基因组关联研究确定了 30 个与双相情感障碍相关的位点。
Nat Genet. 2019 May;51(5):793-803. doi: 10.1038/s41588-019-0397-8. Epub 2019 May 1.
2
Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis.人类大脑皮层转录组的发育和遗传调控揭示了精神分裂症的发病机制。
Nat Neurosci. 2018 Aug;21(8):1117-1125. doi: 10.1038/s41593-018-0197-y. Epub 2018 Jul 26.
3
Genetic identification of brain cell types underlying schizophrenia.
沉默子变异与人类疾病的关系。
Genome Biol. 2024 Jul 8;25(1):184. doi: 10.1186/s13059-024-03328-1.
4
Massively parallel characterization of regulatory elements in the developing human cortex.大规模平行分析人类大脑皮层发育过程中的调控元件。
Science. 2024 May 24;384(6698):eadh0559. doi: 10.1126/science.adh0559.
5
Engineered serum markers for non-invasive monitoring of gene expression in the brain.用于无创监测大脑中基因表达的工程化血清标志物。
Nat Biotechnol. 2024 Nov;42(11):1717-1725. doi: 10.1038/s41587-023-02087-x. Epub 2024 Jan 10.
6
Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs.全人类大脑区域中偏向性等位基因的转录因子结合为基因表达数量性状位点提供了机制性见解。
bioRxiv. 2023 Oct 9:2023.10.06.561245. doi: 10.1101/2023.10.06.561245.
7
Clustering Schizophrenia Genes by Their Temporal Expression Patterns Aids Functional Interpretation.通过其时间表达模式聚类精神分裂症基因有助于功能解释。
Schizophr Bull. 2024 Mar 7;50(2):327-338. doi: 10.1093/schbul/sbad140.
8
Massively parallel characterization of psychiatric disorder-associated and cell-type-specific regulatory elements in the developing human cortex.发育中的人类皮质中精神疾病相关和细胞类型特异性调控元件的大规模平行表征
bioRxiv. 2023 Feb 16:2023.02.15.528663. doi: 10.1101/2023.02.15.528663.
9
The relationship between case-control differential gene expression from brain tissue and genetic associations in schizophrenia.精神分裂症脑组织病例对照差异基因表达与遗传关联之间的关系。
Am J Med Genet B Neuropsychiatr Genet. 2023 Jul-Sep;192(5-6):85-92. doi: 10.1002/ajmg.b.32931. Epub 2023 Jan 18.
10
Single-Nuclei RNA Sequencing of 5 Regions of the Human Prenatal Brain Implicates Developing Neuron Populations in Genetic Risk for Schizophrenia.单细胞 RNA 测序揭示人类产前大脑 5 个区域的发育神经元群体与精神分裂症的遗传风险有关。
Biol Psychiatry. 2023 Jan 15;93(2):157-166. doi: 10.1016/j.biopsych.2022.06.033. Epub 2022 Jul 15.
精神分裂症相关脑细胞类型的遗传鉴定。
Nat Genet. 2018 Jun;50(6):825-833. doi: 10.1038/s41588-018-0129-5. Epub 2018 May 21.
4
Opportunities for Neurodevelopmental Plasticity From Infancy Through Early Adulthood.从婴儿期到成年早期的神经发育可塑性机会。
Child Dev. 2018 May;89(3):687-697. doi: 10.1111/cdev.13073. Epub 2018 Apr 17.
5
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.常见的精神分裂症等位基因在突变不耐受基因和受强烈背景选择的区域中富集。
Nat Genet. 2018 Mar;50(3):381-389. doi: 10.1038/s41588-018-0059-2. Epub 2018 Feb 26.
6
Brain Transcriptome Databases: A User's Guide.脑转录组数据库:用户指南。
J Neurosci. 2018 Mar 7;38(10):2399-2412. doi: 10.1523/JNEUROSCI.1930-17.2018. Epub 2018 Feb 7.
7
Studying individual differences in human adolescent brain development.研究人类青少年大脑发育的个体差异。
Nat Neurosci. 2018 Mar;21(3):315-323. doi: 10.1038/s41593-018-0078-4. Epub 2018 Feb 5.
8
Mouse Genome Database (MGD)-2018: knowledgebase for the laboratory mouse.小鼠基因组数据库(MGD)-2018:实验小鼠知识库。
Nucleic Acids Res. 2018 Jan 4;46(D1):D836-D842. doi: 10.1093/nar/gkx1006.
9
Genetic insights into the neurodevelopmental origins of schizophrenia.精神分裂症神经发育起源的遗传学研究进展。
Nat Rev Neurosci. 2017 Dec;18(12):727-740. doi: 10.1038/nrn.2017.125. Epub 2017 Oct 26.
10
Developmental Differences Between Schizophrenia and Bipolar Disorder.精神分裂症与双相情感障碍的发展差异。
Schizophr Bull. 2017 Oct 21;43(6):1176-1189. doi: 10.1093/schbul/sbx126.