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2013 Fiscal Year Final Research Report

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules

Research Project

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Project/Area Number 23390275
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionJichi Medical University

Principal Investigator

YAMAGATA Takanori  自治医科大学, 医学部, 教授 (00239857)

Co-Investigator(Renkei-kenkyūsha) NAGATA Kouichi  愛知県心身障害者コロニー発達障害研究所, 神経制御学部, 部長 (50252143)
MIRI Masato  自治医科大学, 医学部, 講師 (10337347)
NOZAKI Yasuyuki  自治医科大学, 医学部, 助教 (90281295)
NAKASHIMA Naomi  自治医科大学, 医学部, 助教 (20337330)
MONDEN Yukifumi  自治医科大学, 医学部, 講師 (80382951)
NAGASHIMA Masako  自治医科大学, 医学部, 助教 (70438662)
JINBO Eriko  自治医科大学, 医学部, 講師 (20291651)
Project Period (FY) 2011-04-01 – 2014-03-31
Keywords自閉症スペクトラム障害 / コピー数多型 / 遺伝子変異 / 足場蛋白 / LIN7 / セクレチン / シナプス / G蛋白結合型受容体
Research Abstract

To detect the relating genes and the treatment of autism spectrum disorder (ASD), we analyzed ASD and intellectual disability patients for copy number variation and candidate gene mutation. Scaffolding proteins such as SHANK3 and LIN7A/B were detected as responsible gene. Lin7a/b were considered to have important role on neuronal development because neuronal cell movement and axon elongation were disturbed by blocking the expression of Lin7a/b in fetal brain. We previously detected gene mutations on the G-protein coupled receptors (GPCRs). Addition to them, mutations on secretin receptor gene that is one of the GPCR were detected. Expression of oxytocin and vasopressin were increased after intra-ventricular injection of secretin. These results indicated that scaffolding proteins and GPCRs closely related to ASD and the molecules relating to them were the targets for the treatment research.

  • Research Products

    (26 results)

All 2014 2013 2012 2011

All Journal Article (13 results) (of which Peer Reviewed: 13 results) Presentation (13 results)

  • [Journal Article] LIN7A depletion disrupts cerebral cortex development contributing to intellectual disability in 12q21-deletion syndrome2014

    • Author(s)
      Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo EF, Momoi MY, Nagata K, Yamagata T
    • Journal Title

      PLos One

      Volume: 9 Pages: e92695

    • DOI

      10.1371/journal.pone.0092695

    • Peer Reviewed
  • [Journal Article] Williams-Beuren syndrome with brain malformation and hypertrophic cardiomyopathy2014

    • Author(s)
      Okamoto N, Yamagata T, Yada Y, Ichihashi K, Matsumoto N, Momoi MY, Mizuguchi T
    • Journal Title

      Brain Dev

      Volume: 36 Pages: 523-527

    • DOI

      10.1016/j.braindev.2013.07.002

    • Peer Reviewed
  • [Journal Article] MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus2014

    • Author(s)
      Saito M, Yamagata T, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY
    • Journal Title

      Brain Dev

      Volume: 36 Pages: 64-69

    • DOI

      10.1016/j.braindev.2013.01.004

    • Peer Reviewed
  • [Journal Article] An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities2013

    • Author(s)
      Matsumoto A, Kuwajima M, Miyake K, Kojima K, Nakashima N, Jimbo EF, Kubota T, Momoi MY, Yamagata T
    • Journal Title

      J Hum Genet

      Volume: 58 Pages: 755-757

    • DOI

      10.1038/jhg.2013.88

    • Peer Reviewed
  • [Journal Article] Clinical correlations of mutations affecting six components of the SWI/SNF complex : Detailed description of 21 patients and a review of the literature2013

    • Author(s)
      Kosho T, Okamoto N, Ohashi H, Yamagata T, Matsumoto N (27人中11番目)
    • Journal Title

      Am J Med Genet A

      Volume: 161 Pages: 1221-1237

    • DOI

      10.1002/ajmg.a.35933

    • Peer Reviewed
  • [Journal Article] Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation2013

    • Author(s)
      Kato M, Yamagata T, Kubota M, Arai H, Saitsu H(27人中2番目)
    • Journal Title

      Epilepsia

      Volume: 54 Pages: 1282-7

    • DOI

      10.1111/epi.12200

    • Peer Reviewed
  • [Journal Article] Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers2013

    • Author(s)
      Monden Y, Mori M, Kuwajima M, Goto T, Yamagata T, Momoi MY
    • Journal Title

      Brain Dev

      Volume: 35 Pages: 582-585

    • DOI

      10.1016/j.braindev.2012.08.006

    • Peer Reviewed
  • [Journal Article] Contiguous ABCD1 DXS1357E deletion syndrome : Report of an autopsy case2013

    • Author(s)
      Iwasa M, Yamagata T, Mizuguchi M, Itoh M, Matsumoto A, Hironaka M, Honda A, Momoi MY, Shimozawa N
    • Journal Title

      Neuropathology

      Volume: 33 Pages: 292-298

    • DOI

      10.1111/j.1440-1789.2012.01348.x

    • Peer Reviewed
  • [Journal Article] Mutation in Parkinson disease-associated, G-protein coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder2012

    • Author(s)
      Fujita-Jimbo E, Yu ZL, Li H, Yamagata T, Mori M, Momoi T, Momoi MY
    • Journal Title

      PLoS One

      Volume: 7 Pages: e51155

    • Peer Reviewed
  • [Journal Article] Right prefrontal activation as a neuro-functional biomarker for monitoring acute effects of methylphenidate in ADHD children : an fNIRS study2012

    • Author(s)
      Monden Y, Dan I, Dan H, Nagashima M, Tsuzuki D, Kyutoku Y, Gunji Y, Yamagata T, Watanabe E, Momoi MY
    • Journal Title

      NeuroImage Clinical

      Volume: 1 Pages: 131-40

    • DOI

      10.1016/j.nicl.2012.10.001

    • Peer Reviewed
  • [Journal Article] Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination2012

    • Author(s)
      Shimojima K, Okamoto N, Suzuki Y, Saito M, Mori M, Yamagata T, Momoi MY, Hattori H, Okano Y, Hisata K, Okumura A, Yamamoto T
    • Journal Title

      J Hum Genet

      Volume: 57 Pages: 593-600

    • DOI

      10.1038/jhg.2012.77

    • Peer Reviewed
  • [Journal Article] Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome2012

    • Author(s)
      Tsurusaki Y, Okamoto N, Ohashi H, Kosho T, Yamagata T, Matsumoto N(31人中15番目)
    • Journal Title

      Nat Genet

      Volume: 44 Pages: 376-378

    • DOI

      10.1038/ng.2219

    • Peer Reviewed
  • [Journal Article] Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS2012

    • Author(s)
      Monden Y, Dan H, Nagashima M, Dan I, Kyutoku Y, Okamoto M, Yamagata T, Momoi MY, Watanabe E
    • Journal Title

      Clin Neurophysiol

      Volume: 123 Pages: 1147-1157

    • DOI

      10.1016/j.clinph.2011.10.006

    • Peer Reviewed
  • [Presentation] 自閉症スペクトラム障害の評価 : 統一した評価法の必要性2014

    • Author(s)
      山形崇倫, 小島華林, 門田行史
    • Organizer
      第56回日本小児神経学会シンポジウム
    • Place of Presentation
      浜松
    • Year and Date
      20140529-31
  • [Presentation] 自閉性障害原因遺伝子変異と小胞体ストレスの関与2014

    • Author(s)
      小島華林, 神保恵理子, 松本歩, 山形崇倫, 桃井隆, 桃井真里子
    • Organizer
      第56回日本小児神経学会
    • Place of Presentation
      浜松
    • Year and Date
      20140529-31
  • [Presentation] 自閉性障害患者における時計関連遺伝子の変異解析2014

    • Author(s)
      松本歩, 楊志亮, 小島華林, 中山一大, 神保恵理子, 岩本禎彦, 永田浩一, 山形崇倫
    • Organizer
      第56回日本小児神経学会
    • Place of Presentation
      浜松
    • Year and Date
      20140529-31
  • [Presentation] 自閉性障害原因遺伝子 CADM1 に結合する足場タンパク MUPP1 の遺伝子変異解析2014

    • Author(s)
      楊志亮, 小島華林, 神保恵理子, 山形崇倫, 桃井隆, 桃井真里子
    • Organizer
      第56回日本小児神経学会
    • Place of Presentation
      浜松
    • Year and Date
      20140529-31
  • [Presentation] Contribution of Scaffold proteins to developmental disorder2013

    • Author(s)
      Matsumoto A, Mizuno M, Hamada N, Jimbo EF, Kojima K, Momoi MY, Nagata K, Yamagata T
    • Organizer
      The 63rd Annual Meeting for the American Society of Human Genetics
    • Place of Presentation
      Boston
    • Year and Date
      20131022-26
  • [Presentation] Mutations in Secretin receptor may be related to autism spectrum disorder2013

    • Author(s)
      Kojima K, Yamagata T, Matsumoto A, Jimbo EF, Momoi MY
    • Organizer
      The 63rd Annual Meeting for the American Society of Human Genetics
    • Place of Presentation
      Boston
    • Year and Date
      20131022-26
  • [Presentation] 発達障害患者 CNV 領域におけるシナプス関連分子の解析2013

    • Author(s)
      山形崇倫, 松本歩, 永田浩一
    • Organizer
      第55回日本小児神経学会シンポジウム
    • Place of Presentation
      大分
    • Year and Date
      20130529-0601
  • [Presentation] 発達障害患者 CNV領域におけるシナプス関連分子の解析2013

    • Author(s)
      松本歩, 山形崇倫, 野崎靖之, 神保恵理子, 永田浩一, 桃井真里子
    • Organizer
      第55回日本小児神経学会
    • Place of Presentation
      大分
    • Year and Date
      20130529-0601
  • [Presentation] Mutation in Secretin receptor gene in Autism spectrum disorder and genes regulated by secretin in the brain2012

    • Author(s)
      Kojima K, Yamagata T, Matsumoto A, Saito M, Jimbo EF, Momoi MY
    • Organizer
      The 62rd Annual Meeting for the American Society of Human Genetics
    • Place of Presentation
      San Francisco
    • Year and Date
      20121106-09
  • [Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Mental Retardation2012

    • Author(s)
      Matsumoto A, Yamagata T, Nozaki Y, Jimbo EF, Momoi MY
    • Organizer
      The 62rd Annual Meeting for the American Society of Human Genetics
    • Place of Presentation
      San Francisco
    • Year and Date
      20121106-09
  • [Presentation] RPS6KA3 の重複を認めた軽度知的障害男児例2012

    • Author(s)
      松本歩, 山形崇倫, 桑島真理, 神保恵理子, 桃井真里子
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      20121024-27
  • [Presentation] Cadm1 変異を持つ自閉性障害患者のリンパ芽球を用いた小胞体ストレス感受性についての検討2012

    • Author(s)
      小島華林, 松本歩, 楊志亮, 神保恵理子, 山形崇倫, 桃井真里子
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      20121024-27
  • [Presentation] Deletion of MAOA and MAOB in male siblings with severe mental retardation and autistic phenotype2011

    • Author(s)
      Saito M, Yamagata T, Shiba Y, Nakashima N, Nagashima M, Jimbo E, Momoi MY
    • Organizer
      The 62rd Annual Meeting for the American Society of Human Genetics
    • Place of Presentation
      Montreal
    • Year and Date
      20111011-15

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Published: 2015-06-25  

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