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Investigation of DNA methylation in neural cells of the child after abuse

Research Project

Project/Area Number 25670340
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Legal medicine
Research InstitutionGunma University

Principal Investigator

Kominato Yosihhiko  群馬大学, 医学(系)研究科(研究院), 教授 (30205512)

Co-Investigator(Kenkyū-buntansha) SANO RIE  群馬大学, 大学院医学系研究科, 講師 (70455955)
YOICHIRO TAKAHASHI  群馬大学, 大学院医学系研究科, 助教 (50640538)
中島 たみ子  群馬大学, 医学(系)研究科(研究院), 研究員 (40008561)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywords法医学 / 虐待 / DNAメチル化 / 子どもの虐待
Outline of Final Research Achievements

Child abuse is assumed to cause stress reaction resulting in secretion of corticotropin releasing hormone (CRH) from hypothalamus, adrenocorticotropic hormone from pituitary and glucocorticoid from adrenal gland. The CRH elevation could be involved in psychological disturbance. DNA methylation was reported to be enhanced in the promoter of the gene encoding the glucocorticoid receptor (NR3C1) of the suicide cases who had experienced child abuse. DNA methylation of the promoter in NR3C1 was examined from neurons of the hippocampus of the child with abuse. Using DNA prepared from neurons in paraffin embodied tissues from hippocampus of the child with abuse and controls with endogenous diseases, bisulfite genomic sequencing was carried out, showing increased DNA methylation of the promoter in NR3C1 in the neurons of the hippocampus in the child with abuse. On the basis of the results, DNA methylation in the neurons of the hippocampus could be one of the candidates implying child abuse.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (14 results)

All 2015 2014 2013

All Journal Article (8 results) (of which Peer Reviewed: 8 results,  Open Access: 5 results,  Acknowledgement Compliant: 4 results) Presentation (6 results)

  • [Journal Article] A 3.0-kb delation including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype2015

    • Author(s)
      Sano R, Kuboya E, Nakajima T, Takahashi Y, Takahashi K, Kubo R, Kominato Y, Takeshita H, Yamao H, Kishida T, Isa K, Ogasawara K, Uchikawa M
    • Journal Title

      Vox Sang

      Volume: 108 Issue: 3 Pages: 310-313

    • DOI

      10.1111/vox.12216

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Blood group gene is barely expressed in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element2015

    • Author(s)
      Sano R, Nogawa T, Nakajima T, Takahashi Y, Kubo R, Kominato Y, Yokohama A, Tsukada J, Yamao H, Kishida T, Ogasawara K, Uchikawa M
    • Journal Title

      Vox Sang

      Volume: 108 Issue: 3 Pages: 302-309

    • DOI

      10.1111/vox.12220

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively2014

    • Author(s)
      Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Michino J, Masuno A, Tsuneyama H, Ito S, Ogasawara K, Uchikawa M
    • Journal Title

      Vox Sang

      Volume: 107 Issue: 2 Pages: 171-180

    • DOI

      10.1111/vox.12136

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype.2014

    • Author(s)
      Takahashi Y, Isa K, Sano R, Nakajima T, Kubo R, Takahashi K, Kominato Y, Tsuneyama H, Ogasawara K, Uchikawa M
    • Journal Title

      Vox Sang

      Volume: 106 Issue: 2 Pages: 167-175

    • DOI

      10.1111/vox.12077

    • Related Report
      2014 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Evaluation of all non-synonymous single nucleotide polymorphisms (SNPs) in the genes encoding human deoxyribonuclease I and I-like 3 as a functional SNP potentially implicated in autoimmunity2014

    • Author(s)
      Misuzu Ueki
    • Journal Title

      FEBS Journal

      Volume: 281 Issue: 1 Pages: 376-390

    • DOI

      10.1111/febs.12608

    • Related Report
      2013 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual2013

    • Author(s)
      Tamiko Nakajima
    • Journal Title

      Transfusion

      Volume: 53 Issue: 11pt2 Pages: 2917-2927

    • DOI

      10.1111/trf.12181

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Usefulness of postmortem computed tomography for demonstrating cerebral hemorrhage in a brain too fragile for macroscopic examination.2013

    • Author(s)
      Takahashi Y, Sano R, Kominato Y, Takei H, Kobayashi S, Shimada T, Awata S, Hirasawa S
    • Journal Title

      Journal of Forensic Radiology and Imaging

      Volume: 1 Pages: 212-214

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Use of postmortem computed tomography to reveal acute subdural hematoma in a severely decomposed body with advanced skeletonization.2013

    • Author(s)
      Sano R, Hirasawa S, Awata S, Kobayashi S, Shimada T, Takei H, Takahashi Y, Kominato Y
    • Journal Title

      Leg Med

      Volume: 15 Issue: 1 Pages: 32-34

    • DOI

      10.1016/j.legalmed.2012.05.005

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] Bm型では赤血球系細胞においてB遺伝子の発現が極めて低下している-CD34陽性細胞を用いた赤血球系細胞への分化培養実験-.2015

    • Author(s)
      佐野利恵、中島たみ子、高橋遥一郎、小湊慶彦
    • Organizer
      日本DNA多型学会第24回学術集会
    • Place of Presentation
      岡山県岡山市
    • Year and Date
      2015-11-19
    • Related Report
      2015 Annual Research Report
  • [Presentation] ABO遺伝子血球系特異的エンハンサー内GATAサイトの一塩基置換がB抗原量の低下をもたらしたBm型一症例.2013

    • Author(s)
      佐野利恵, 中島たみ子, 高橋遥一郎, 高橋圭子, 藤原純子, 竹下治男, 安田年博, 小湊慶彦, 岸田哲子.
    • Organizer
      日本DNA多型学会第22回学術集会.
    • Place of Presentation
      仙台
    • Related Report
      2013 Research-status Report
  • [Presentation] VKORC1遺伝子に座位する6SNPsのアジア人多集団での分布.2013

    • Author(s)
      藤原純子,竹下治男,木村かおり,安田年博,佐野利恵, 中島たみ子,小湊慶彦
    • Organizer
      日本DNA多型学会第22回学術集会.
    • Place of Presentation
      仙台
    • Related Report
      2013 Research-status Report
  • [Presentation] ABO式血液型遺伝子エンハンサー欠損がBm型の原因である2013

    • Author(s)
      佐野利恵, 中島たみ子, 高橋遥一郎, 小湊慶彦.
    • Organizer
      第9回麒麟塾
    • Place of Presentation
      東京
    • Related Report
      2013 Research-status Report
  • [Presentation] ABO遺伝子血球系特異的エンハンサー内GATAサイトの一塩基置換がB抗原量の低下をもたらしたBm型一症例2013

    • Author(s)
      佐野利恵, 中島たみ子, 高橋遥一郎, 高橋圭子, 竹下治男, 安田年博, 小湊慶彦
    • Organizer
      第97次日本法医学会学術全国集会
    • Place of Presentation
      札幌
    • Related Report
      2013 Research-status Report
  • [Presentation] 日本人のBm型に関する遺伝子の解析.2013

    • Author(s)
      伊佐和美, 小笠原健一, 佐々木佳奈, 岡崎仁, 田所憲治, 國井七絵, 小野寺孝行, 斎藤昌子, 常山初江, 矢部隆一, 内川誠, 佐野利恵, 中島たみ子, 小湊慶彦, 丸橋隆行, 横濱章彦.
    • Organizer
      第61回日本輸血・細胞治療学会総会.
    • Place of Presentation
      横浜
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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