The VNTR of the AS3MT gene is associated with brain activations during a memory span task and their training-induced plasticity
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 ro...
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Published in | Psychological medicine Vol. 51; no. 11; pp. 1927 - 1932 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Cambridge, UK
Cambridge University Press
01.08.2021
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Abstract | 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.
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.
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.
This study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training. |
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AbstractList | BackgroundThe 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.MethodsWe 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.ResultsThe 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.ConclusionsThis study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training. 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.BACKGROUNDThe 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.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.METHODSWe 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.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.RESULTSThe 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.This study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training.CONCLUSIONSThis study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training. 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. 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. 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. This study sheds light on the role of AS3MT gene variants in neural plasticity related to memory span training. |
Author | Chen, Xiongying Xiang, Yu-Tao Dong, Qi Du, Boqi Chen, Chuansheng Li, Xiaohong Wang, Chuanyue Li, Jun Ji, Feng Zhang, Qiumei Li, Yang Deng, Xiaoxiang Zhao, Wan |
AuthorAffiliation | 2 School of Public Health, Jining Medical University , 45# Jianshe South Road, Jining 272013 , Shandong Province , P.R. China 5 Faculty of Health Sciences, University of Macau, Avenida da Universidade , Taipa , Macau 1 State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University , Beijing , P.R. China 4 School of Mental Health, Jining Medical University , 45# Jianshe South Road, Jining 272013 , Shandong Province , P.R. China 6 Department of Psychology and Social Behavior, University of California , Irvine , CA 92697 , USA 3 The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders & the Advanced Innovation Center for Human Brain Protection, Beijing Anding Hospital, School of Mental Health, Capital Medical University , Beijing 100088 , China |
AuthorAffiliation_xml | – name: 5 Faculty of Health Sciences, University of Macau, Avenida da Universidade , Taipa , Macau – name: 6 Department of Psychology and Social Behavior, University of California , Irvine , CA 92697 , USA – name: 2 School of Public Health, Jining Medical University , 45# Jianshe South Road, Jining 272013 , Shandong Province , P.R. China – name: 4 School of Mental Health, Jining Medical University , 45# Jianshe South Road, Jining 272013 , Shandong Province , P.R. China – name: 1 State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University , Beijing , P.R. China – name: 3 The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders & the Advanced Innovation Center for Human Brain Protection, Beijing Anding Hospital, School of Mental Health, Capital Medical University , Beijing 100088 , China |
Author_xml | – sequence: 1 givenname: Wan surname: Zhao fullname: Zhao, Wan organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China – sequence: 2 givenname: Qiumei surname: Zhang fullname: Zhang, Qiumei organization: 2School of Public Health, Jining Medical University, 45# Jianshe South Road, Jining 272013, Shandong Province, P.R. China – sequence: 3 givenname: Xiongying surname: Chen fullname: Chen, Xiongying organization: 3The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders & the Advanced Innovation Center for Human Brain Protection, Beijing Anding Hospital, School of Mental Health, Capital Medical University, Beijing 100088, China – sequence: 4 givenname: Yang surname: Li fullname: Li, Yang organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China – sequence: 5 givenname: Xiaohong surname: Li fullname: Li, Xiaohong organization: 3The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders & the Advanced Innovation Center for Human Brain Protection, Beijing Anding Hospital, School of Mental Health, Capital Medical University, Beijing 100088, China – sequence: 6 givenname: Boqi surname: Du fullname: Du, Boqi organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China – sequence: 7 givenname: Xiaoxiang surname: Deng fullname: Deng, Xiaoxiang organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China – sequence: 8 givenname: Feng surname: Ji fullname: Ji, Feng organization: 4School of Mental Health, Jining Medical University, 45# Jianshe South Road, Jining 272013, Shandong Province, P.R. China – sequence: 9 givenname: Chuanyue surname: Wang fullname: Wang, Chuanyue organization: 3The National Clinical Research Center for Mental Disorders & Beijing Key Laboratory of Mental Disorders & the Advanced Innovation Center for Human Brain Protection, Beijing Anding Hospital, School of Mental Health, Capital Medical University, Beijing 100088, China – sequence: 10 givenname: Yu-Tao surname: Xiang fullname: Xiang, Yu-Tao organization: 5Faculty of Health Sciences, University of Macau, Avenida da Universidade, Taipa, Macau – sequence: 11 givenname: Qi surname: Dong fullname: Dong, Qi organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China – sequence: 12 givenname: Chuansheng surname: Chen fullname: Chen, Chuansheng organization: 6Department of Psychology and Social Behavior, University of California, Irvine, CA 92697, USA – sequence: 13 givenname: Jun orcidid: 0000-0002-9231-1791 surname: Li fullname: Li, Jun email: lijundp@bnu.edu.cn organization: 1State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, P.R. China |
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Snippet | The Arsenic (+3 oxidation state) methyltransferase (AS3MT) gene has been identified as a top risk gene for schizophrenia in several large-scale genome-wide... BackgroundThe Arsenic (+3 oxidation state) methyltransferase (AS3MT) gene has been identified as a top risk gene for schizophrenia in several large-scale... |
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SubjectTerms | Adult Arsenic Brain - physiology Brain activity Brain mapping Brain research China Cortex Cortex (cingulate) Cortex (parietal) Data analysis DNA methylation Female Functional magnetic resonance imaging Genome-wide association studies Genome-Wide Association Study Genomes Genomics Gyrus Cinguli - physiology Head movements Healthy Volunteers Humans Learning Magnetic Resonance Imaging Male Memory Memory - physiology Memory span Mental disorders Mental task performance Methyltransferase Methyltransferases - genetics Minisatellite Repeats Neostriatum Neuroimaging Neuronal Plasticity Neuroplasticity Original Original Article Oxidation Parietal cortex Parietal Lobe - physiology Plasticity Prefrontal cortex Prefrontal Cortex - physiology Quantitative trait loci Schizophrenia Schizophrenia - genetics Variants Young Adult |
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Title | The VNTR of the AS3MT gene is associated with brain activations during a memory span task and their training-induced plasticity |
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