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Neural tube defect manifestation due to the interaction of genetic mutation and Ochratoxin A in the genetic polydactyly/ arhinencephaly mouse embryo, Pdn/Pdn

Research Project

Project/Area Number 22591200
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Embryonic/Neonatal medicine
Research InstitutionTottori University

Principal Investigator

UETA Etsuko  鳥取大学, 医学部, 講師 (40335526)

Co-Investigator(Kenkyū-buntansha) NARUSE Ichiro  鳥取大学, 医学部, 教授 (20113326)
Project Period (FY) 2010 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2012: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords先天異常学 / Gli3 / 神経管閉鎖障害 / オクラトキシンA / オクラトキシンA
Research Abstract

Ochratoxin A (OTA) is a teratogen causing neural tube defects (NTDs) in mice. We analyzed the gene expression by using the genetic polydactyly/arhinencephaly mouse (Pdn/Pdn) to examine the pathogenesis of NTDs. After treatment with 2 mg/kg of OTA to Pdn/+ female mice, mated with Pdn/+ male, on day 7.5 of gestation, gene expressions in the embryo were analyzed by DNA microarray, real-time PCR and whole mount in situ hybridiyzation (WISH) on day 9 of gestation. From these investigations, it was suggested that NTDs induced by OTA may be the result of altered multiple expressions in Pdn/Pdn embryos.

Report

(4 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • Research Products

    (23 results)

All 2012 2011 2010 Other

All Journal Article (12 results) (of which Peer Reviewed: 3 results) Presentation (11 results)

  • [Journal Article] et al Altered gene expression induced by ochratoxin A in genetic polydactyly /arhinencephaly mouse embryo, Pdn/Pdn2012

    • Author(s)
      Ueta E
    • Journal Title

      Congenital Anomalies

      Volume: 52(4)

    • Related Report
      2012 Final Research Report
  • [Journal Article] et al Alterations of gene expression by ochratoxin A in geneticpolydactyly /arhinencephaly mouse embryos2012

    • Author(s)
      Toya Y., Ueta E.
    • Journal Title

      Congenital Anomalies

      Volume: 52(4)

    • Related Report
      2012 Final Research Report
  • [Journal Article] Altered gene expression induced by ochratoxin A in genetic polydactyly /arhinencephaly mouse embryo, Pdn/Pdn2012

    • Author(s)
      Ueta E., et al
    • Journal Title

      Congenital Anomalies

      Volume: 52(4)

    • Related Report
      2012 Annual Research Report
  • [Journal Article] Alterations of gene expression by ochratoxin A in genetic polydactyly /arhinencephaly mouse embryos2012

    • Author(s)
      Toya Y, et al
    • Journal Title

      Congenital Anomalies

      Volume: 52(4)

    • Related Report
      2012 Annual Research Report
  • [Journal Article] et al Altered gene expression induced by ochratoxin A in geneticpolydactyly/arhinencephaly mouse embryo, Pdn/Pdn2011

    • Author(s)
      Ueta E
    • Journal Title

      Congenital Anomalies

      Volume: 51(4)

    • Related Report
      2012 Final Research Report
  • [Journal Article] Altered gene expression induced bv ochratoxin A in genetic polydactyly/arhinencephaly mouse embryo, Pdn/Pdn2011

    • Author(s)
      Ueta E., et al
    • Journal Title

      Congenital Anomalies

      Volume: 51(4)

    • Related Report
      2011 Annual Research Report
  • [Journal Article] et al Syndromes Caused by the Mutations in GLI3 Gene2010

    • Author(s)
      Naruse I.
    • Journal Title

      Current Pediatric Reviews

      Volume: 6 Pages: 219-225

    • Related Report
      2012 Final Research Report
  • [Journal Article] et al Gender-dependent differences in the incidence of ochratoxin A-induced neural tube defects in Pdn/Pdn mouse2010

    • Author(s)
      Ueta E
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 29-39

    • Related Report
      2012 Final Research Report
  • [Journal Article] et al Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes2010

    • Author(s)
      Naruse I
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 1-7

    • Related Report
      2012 Final Research Report
  • [Journal Article] Syndromes Caused by the Mutations in GLI3 Gene.2010

    • Author(s)
      Naruse I., et al
    • Journal Title

      Current Pediatric Reviews

      Volume: 6 Pages: 219-225

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Gender-dependent differences in the incidence of ochratoxin A-induced neural tube defects in Pdn/Pdn mouse.2010

    • Author(s)
      Ueta E., et al
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 29-39

    • NAID

      10029577445

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes.2010

    • Author(s)
      Naruse I., et al
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 1-7

    • NAID

      10029577246

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Presentation] 遺伝性多指症/無嗅脳症マウス胚におけるOchratoxin Aによる遺伝子発現の変動2012

    • Author(s)
      鳥谷裕太郎、上田悦子、成瀬一郎
    • Organizer
      第52回日本先天異常学会学術集会
    • Place of Presentation
      東京都新宿区 東京女子医科大学
    • Year and Date
      2012-07-08
    • Related Report
      2012 Final Research Report
  • [Presentation] 神経管閉鎖期におけるOchratoxin A曝露による遺伝子の発現変化2012

    • Author(s)
      上田悦子、鳥谷裕太郎、成瀬一郎、曽根保子、大塚譲
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京都新宿区 東京女子医科大学
    • Year and Date
      2012-07-06
    • Related Report
      2012 Final Research Report
  • [Presentation] Gli3変異とオクラトキシンA曝露による神経管閉鎖障害発症における遺伝子発現の変動2011

    • Author(s)
      上田悦子、鳥谷裕太郎、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京都千代田区 シェーンバッハサボー
    • Year and Date
      2011-07-22
    • Related Report
      2012 Final Research Report
  • [Presentation] Gli3変異とオクラトキシンA曝露による神経管閉鎖障害発症における遺伝子発現の変動2011

    • Author(s)
      上田悦子
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京都千代田区シェーンバッハサボー
    • Year and Date
      2011-07-22
    • Related Report
      2011 Annual Research Report
  • [Presentation] オクラトキシンAと転写因子Gli3による神経管閉鎖障害発症と脳形態形成関連遺伝子の発現変化2011

    • Author(s)
      上田悦子、曽根保子 大塚譲、成瀬一郎
    • Organizer
      日本栄養食糧学会
    • Place of Presentation
      東京都文京区 お茶の水女子大学
    • Year and Date
      2011-05-13
    • Related Report
      2012 Final Research Report
  • [Presentation] オクラトキシンAと転写因了Gli3による神経管閉鎖障害発症と脳形態形成関連遺伝子の発現変化2011

    • Author(s)
      上田悦子
    • Organizer
      日本栄養食糧学会
    • Place of Presentation
      東京都文京区お茶の水女子大学
    • Year and Date
      2011-05-13
    • Related Report
      2011 Annual Research Report
  • [Presentation] オクラトキシンA曝露による神経管閉鎖障害と性関連遺伝子の変動2010

    • Author(s)
      上田悦子、角野良紀、小川将也、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      淡路市 淡路夢舞台国際会議場
    • Year and Date
      2010-07-08
    • Related Report
      2012 Final Research Report 2010 Annual Research Report
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差 -第3報-2010

    • Author(s)
      角野良紀、上田悦子、小川将也、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      淡路市 淡路夢舞台国際会議場
    • Year and Date
      2010-07-08
    • Related Report
      2012 Final Research Report
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差-第3報-2010

    • Author(s)
      角野良紀
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      淡路市 淡路夢舞台国際会議場
    • Year and Date
      2010-07-08
    • Related Report
      2010 Annual Research Report
  • [Presentation] 神経管閉鎖期におけるOchratoxin A曝露による遺伝子の発現変化

    • Author(s)
      上田 悦子
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京女子医科大学
    • Related Report
      2012 Annual Research Report
  • [Presentation] 遺伝性多指症/無嗅脳症マウス胚におけるOchratoxin Aによる遺伝子発現の変動

    • Author(s)
      鳥谷 裕太郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京女子医科大学
    • Related Report
      2012 Annual Research Report

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Published: 2010-08-23   Modified: 2019-07-29  

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