• 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

基因的 VNTR 与记忆广度任务期间的大脑激活及其训练诱导的可塑性有关。

The VNTR of the gene is associated with brain activations during a memory span task and their training-induced plasticity.

机构信息

State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China.

School of Public Health, Jining Medical University, 45# Jianshe South Road, Jining272013, Shandong Province, P.R. China.

出版信息

Psychol Med. 2021 Aug;51(11):1927-1932. doi: 10.1017/S0033291720000720. Epub 2020 Apr 20.

DOI:10.1017/S0033291720000720
PMID:32308175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8381288/
Abstract

BACKGROUND

The Arsenic (+3 oxidation state) methyltransferase (AS3MT) gene has been identified as a top risk gene for schizophrenia in several large-scale genome-wide association studies. A variable number tandem repeat (VNTR) of this gene is the most significant expression quantitative trait locus, but its role in brain activity in vivo is still unknown.

METHODS

We first performed a functional magnetic resonance imaging (fMRI) scan of 101 healthy subjects during a memory span task, trained all subjects on an adaptive memory span task for 1 month, and finally performed another fMRI scan after the training. After excluding subjects with excessive head movements for one or more scanning sessions, data from 93 subjects were included in the final analyses.

RESULTS

The VNTR was significantly associated with both baseline brain activation and training-induced changes in multiple regions including the prefrontal cortex and the anterior and posterior cingulate cortex. Additionally, it was associated with baseline brain activation in the striatum and the parietal cortex. All these results were corrected based on the family-wise error rate method across the whole brain at the peak level.

CONCLUSIONS

This study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training.

摘要

背景

砷(+3 氧化态)甲基转移酶(AS3MT)基因已被确定为几个大规模全基因组关联研究中精神分裂症的首要风险基因。该基因的可变数串联重复(VNTR)是最显著的表达数量性状基因座,但它在体内大脑活动中的作用仍不清楚。

方法

我们首先对 101 名健康受试者在记忆跨度任务期间进行了功能磁共振成像(fMRI)扫描,对所有受试者进行了为期 1 个月的适应性记忆跨度任务训练,最后在训练后进行了另一次 fMRI 扫描。在排除了一个或多个扫描会话中头部运动过多的受试者后,93 名受试者的数据被纳入最终分析。

结果

VNTR 与包括前额叶皮层、前后扣带回皮层在内的多个区域的基线大脑激活以及训练引起的变化显著相关。此外,它还与纹状体和顶叶皮层的基线大脑激活有关。所有这些结果都在全脑峰值水平上基于组内错误率方法进行了校正。

结论

这项研究揭示了 AS3MT 基因变异在与记忆跨度训练相关的神经可塑性中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1176/8381288/fe0ed39ef073/S0033291720000720_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1176/8381288/f2f642ad16e4/S0033291720000720_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1176/8381288/fe0ed39ef073/S0033291720000720_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1176/8381288/f2f642ad16e4/S0033291720000720_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1176/8381288/fe0ed39ef073/S0033291720000720_fig2.jpg

相似文献

1
The VNTR of the gene is associated with brain activations during a memory span task and their training-induced plasticity.基因的 VNTR 与记忆广度任务期间的大脑激活及其训练诱导的可塑性有关。
Psychol Med. 2021 Aug;51(11):1927-1932. doi: 10.1017/S0033291720000720. Epub 2020 Apr 20.
2
Effect of ZNF804A gene polymorphism (rs1344706) on the plasticity of the functional coupling between the right dorsolateral prefrontal cortex and the contralateral hippocampal formation.ZNF804A 基因多态性(rs1344706)对右侧背外侧前额叶皮层和对侧海马结构之间功能连接可塑性的影响。
Neuroimage Clin. 2020;27:102279. doi: 10.1016/j.nicl.2020.102279. Epub 2020 May 26.
3
Neural plasticity in amplitude of low frequency fluctuation, cortical hub construction, regional homogeneity resulting from working memory training.工作记忆训练引起低频振幅的神经可塑性、皮质中枢构建、区域同质性。
Sci Rep. 2017 May 3;7(1):1470. doi: 10.1038/s41598-017-01460-6.
4
A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.一个人类特异性的 AS3MT 同种型和 BORCS7 是 10q24.32 精神分裂症相关位点的分子风险因素。
Nat Med. 2016 Jun;22(6):649-56. doi: 10.1038/nm.4096. Epub 2016 May 9.
5
Increased prefrontal and parietal activity after training of working memory.工作记忆训练后前额叶和顶叶活动增强。
Nat Neurosci. 2004 Jan;7(1):75-9. doi: 10.1038/nn1165. Epub 2003 Dec 14.
6
Converging genetic and functional brain imaging evidence links neuronal excitability to working memory, psychiatric disease, and brain activity.融合的遗传和功能脑成像证据将神经元兴奋性与工作记忆、精神疾病和大脑活动联系起来。
Neuron. 2014 Mar 5;81(5):1203-1213. doi: 10.1016/j.neuron.2014.01.010. Epub 2014 Feb 13.
7
Diurnal patterns of activity of the orienting and executive attention neuronal networks in subjects performing a Stroop-like task: a functional magnetic resonance imaging study.在执行斯特鲁普样任务的受试者中,定向和执行注意神经网络的活动的昼夜节律模式:一项功能磁共振成像研究。
Chronobiol Int. 2010 Jul;27(5):945-58. doi: 10.3109/07420528.2010.489400.
8
Evidence for the contribution of COMT gene Val158/108Met polymorphism (rs4680) to working memory training-related prefrontal plasticity.COMT 基因 Val158/108Met 多态性(rs4680)对工作记忆训练相关前额叶可塑性的贡献的证据。
Brain Behav. 2020 Feb;10(2):e01523. doi: 10.1002/brb3.1523. Epub 2020 Jan 9.
9
Fronto-striatal hypoactivation during correct information retrieval in patients with schizophrenia: an fMRI study.精神分裂症患者在正确信息检索过程中的额纹状体激活不足:一项功能磁共振成像研究。
Neuroscience. 2008 Apr 22;153(1):54-62. doi: 10.1016/j.neuroscience.2008.01.063. Epub 2008 Feb 15.
10
Altered effect of dopamine transporter 3'UTR VNTR genotype on prefrontal and striatal function in schizophrenia.多巴胺转运体3'非翻译区可变数目串联重复序列(VNTR)基因型对精神分裂症前额叶和纹状体功能的影响改变
Arch Gen Psychiatry. 2009 Nov;66(11):1162-72. doi: 10.1001/archgenpsychiatry.2009.147.

引用本文的文献

1
Chromosome 10q24.32 Variants Associate With Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study.10q24.32 染色体变异与不同人群的脑动脉直径相关:一项全基因组关联研究。
J Am Heart Assoc. 2023 Dec 5;12(23):e030935. doi: 10.1161/JAHA.123.030935. Epub 2023 Dec 1.
2
Structural neuroimaging phenotypes and associated molecular and genomic underpinnings in autism: a review.自闭症中的结构性神经影像表型及其相关的分子和基因组基础:综述
Front Neurosci. 2023 Jun 30;17:1172779. doi: 10.3389/fnins.2023.1172779. eCollection 2023.
3
Chromosome 10q24.32 Variants Associate with Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study.

本文引用的文献

1
Novel inhibitors of As(III) S-adenosylmethionine methyltransferase (AS3MT) identified by virtual screening.通过虚拟筛选鉴定出的新型三价砷 S-腺苷甲硫氨酸甲基转移酶(AS3MT)抑制剂。
Bioorg Med Chem Lett. 2018 Oct 15;28(19):3231-3235. doi: 10.1016/j.bmcl.2018.08.012. Epub 2018 Aug 14.
2
Polymorphism in schizophrenia risk gene is associated with the posterior cingulate Cortex's activation and functional and structural connectivity in healthy controls.精神分裂症风险基因中的多态性与健康对照者后扣带回皮层的激活以及功能和结构连接有关。
Neuroimage Clin. 2018 Apr 3;19:160-166. doi: 10.1016/j.nicl.2018.03.039. eCollection 2018.
3
全基因组关联研究:10号染色体q24.32区域变异与不同人群脑动脉直径相关
medRxiv. 2023 Feb 15:2023.01.31.23285251. doi: 10.1101/2023.01.31.23285251.
4
A Role of DNA Methylation within the CYP17A1 Gene in the Association of Genetic and Environmental Risk Factors with Stress-Related Manifestations of Schizophrenia.CYP17A1 基因内的 DNA 甲基化在遗传和环境风险因素与精神分裂症应激相关表现的关联中的作用。
Int J Mol Sci. 2022 Oct 20;23(20):12629. doi: 10.3390/ijms232012629.
5
Evidence for the contribution of HCN1 gene polymorphism (rs1501357) to working memory at both behavioral and neural levels in schizophrenia patients and healthy controls.HCN1基因多态性(rs1501357)对精神分裂症患者和健康对照者行为及神经水平工作记忆影响的证据。
Schizophrenia (Heidelb). 2022 Aug 20;8(1):66. doi: 10.1038/s41537-022-00271-7.
6
Transcriptomic underpinnings of high and low mirror aggression zebrafish behaviours.高镜像攻击和低镜像攻击斑马鱼行为的转录组学基础
BMC Biol. 2022 May 2;20(1):97. doi: 10.1186/s12915-022-01298-z.
7
Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China.多态性:中国南方儿童癫痫易感性及丙戊酸和奥卡西平治疗药物不良反应的危险因素
Front Neurosci. 2021 Nov 26;15:705297. doi: 10.3389/fnins.2021.705297. eCollection 2021.
8
A Human-Specific Schizophrenia Risk Tandem Repeat Affects Alternative Splicing of a Human-Unique Isoform AS3MTd2d3 and Mushroom Dendritic Spine Density.一个特异性精神分裂症风险串联重复影响人类独特异构体 AS3MTd2d3 的可变剪接和蘑菇状树突棘密度。
Schizophr Bull. 2021 Jan 23;47(1):219-227. doi: 10.1093/schbul/sbaa098.
Working memory training mostly engages general-purpose large-scale networks for learning.
工作记忆训练主要利用通用的大规模网络进行学习。
Neurosci Biobehav Rev. 2018 Oct;93:108-122. doi: 10.1016/j.neubiorev.2018.03.019. Epub 2018 Mar 21.
4
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.全基因组关联分析确定了 30 个精神分裂症的新易感性位点。
Nat Genet. 2017 Nov;49(11):1576-1583. doi: 10.1038/ng.3973. Epub 2017 Oct 9.
5
Mapping the Consequences of Impaired Synaptic Plasticity in Schizophrenia through Development: An Integrative Model for Diverse Clinical Features.通过发育过程描绘精神分裂症中突触可塑性受损的后果:一个针对多种临床特征的综合模型
Trends Cogn Sci. 2017 Oct;21(10):760-778. doi: 10.1016/j.tics.2017.06.006. Epub 2017 Jul 25.
6
Adolescent Stress as a Driving Factor for Schizophrenia Development-A Basic Science Perspective.青少年压力作为精神分裂症发病的驱动因素——基础科学视角
Schizophr Bull. 2017 May 1;43(3):486-489. doi: 10.1093/schbul/sbx033.
7
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.常见的 2p16.1、6p22.1 和 10q24.32 上的变异与汉族人群的精神分裂症有关。
Mol Psychiatry. 2017 Jul;22(7):954-960. doi: 10.1038/mp.2016.212. Epub 2016 Dec 6.
8
The Role of Genes, Stress, and Dopamine in the Development of Schizophrenia.基因、压力和多巴胺在精神分裂症发病中的作用。
Biol Psychiatry. 2017 Jan 1;81(1):9-20. doi: 10.1016/j.biopsych.2016.07.014. Epub 2016 Aug 6.
9
A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus.一个人类特异性的 AS3MT 同种型和 BORCS7 是 10q24.32 精神分裂症相关位点的分子风险因素。
Nat Med. 2016 Jun;22(6):649-56. doi: 10.1038/nm.4096. Epub 2016 May 9.
10
Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.10号染色体q24区域全基因组显著的精神分裂症风险变异与人类大脑中BORCS7、AS3MT和NT5C2的顺式调控改变有关。
Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):806-14. doi: 10.1002/ajmg.b.32445. Epub 2016 Mar 22.