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The regulation of mouse ultrasonic vocalization and behavior by Foxp2

Research Project

Project/Area Number 21700377
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Neuroscience in general
Research InstitutionJichi Medical University

Principal Investigator

JIMBO Eriko  自治医科大学, 医学部, 講師 (20291651)

Project Period (FY) 2009 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
KeywordsFoxp2 / 超音波音声 / マウス / 脳 / 言語障害
Research Abstract

The R553H mutation has been found in the FOXP2 gene of patients with speech-language disorder. Foxp2(R552H) knock-in(KI) mice exhibit impaired ultrasonic vocalization(USV), which is related to human speech and language, and abnormal Purkinje cell development. To clarify the relationship between Foxp2 function in Purkinje cells and USV, we prepared transgenic(Tg) mice that express Foxp2-myc in Purkinje cells. Foxp2 expression in the cerebellum of heterozygous Foxp2(R552H)-KI{Foxp2(R552H)-KI-Pcp2-FOXP2-myc-Tg} mice improved USVs and increased whistle-like sounds. Foxp2 expression promoted dendrite formation in Purkinje cells.

Report

(4 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • 2010 Annual Research Report
  • 2009 Annual Research Report
  • Research Products

    (12 results)

All 2012 2011 2010 2009

All Journal Article (4 results) (of which Peer Reviewed: 4 results) Presentation (8 results)

  • [Journal Article] Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder2012

    • Author(s)
      Fujita, E., Tanabe, Y., Momoi, M. Y., and Momoi, T.
    • Journal Title

      Neurosci Lett

      Volume: 506 Pages: 277-280

    • Related Report
      2011 Annual Research Report 2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it2011

    • Author(s)
      Tanabe, Y., Fujita, E., and Momoi, T
    • Journal Title

      Biochem Biophys Res Commun

      Volume: 410 Pages: 593-596

    • Related Report
      2011 Annual Research Report 2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Genetic factors and epigenetic factors for autism : endoplasmic reticulum stress and impaired synaptic function2009

    • Author(s)
      Momoi, T., Fujita, E., Senoo, H., and Momoi, M
    • Journal Title

      Cell Biol. Int

      Volume: 34 Pages: 13-19

    • Related Report
      2011 Final Research Report
    • Peer Reviewed
  • [Journal Article] Genetic factors and epidemic factors for autism : endoplasmic reticulum stress and impaired synaptic function.2009

    • Author(s)
      Momoi T.
    • Journal Title

      Cell Biol.Int.

      Volume: 34 Pages: 13-19

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Presentation] Catnap2 expression in the cerebellum of the Foxp2(R552H) mice, with mutation related to the speech-language disorder2011

    • Author(s)
      藤田恵理子、田辺裕子、桃井隆、桃井真里子
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2011-12-14
    • Related Report
      2011 Final Research Report
  • [Presentation] Cntnap2 expression in the cerebellum of the Foxp2(R552H) mice, with mutation related to the speech-language disorder2011

    • Author(s)
      藤田恵理子
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2011-12-14
    • Related Report
      2011 Annual Research Report
  • [Presentation] 自閉性障害候補遺伝子CADM1ノックアウトマウスにおける超音波音声2011

    • Author(s)
      藤田恵理子、田辺裕子、桃井隆、桃井真里子
    • Organizer
      第34回日本神経科学大会
    • Place of Presentation
      横浜
    • Year and Date
      2011-09-15
    • Related Report
      2011 Final Research Report
  • [Presentation] 自閉性障害候補遺伝子CADM1ノックアウトマウスにおける超音波音声2011

    • Author(s)
      藤田恵理子
    • Organizer
      第34回日本神経科学大会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2011-09-15
    • Related Report
      2011 Annual Research Report
  • [Presentation] 小脳発達過程におけるフォークヘッドドメインを欠いた新規Foxp2アイソフォームの発現の解析2010

    • Author(s)
      田辺裕子、藤原裕士、松崎鮎美、笠原忠、湯浅茂樹、桃井隆、藤田恵理子
    • Organizer
      第33回日本神経科学大会・第53回日本神経科学会大会・第20回日本神経回路学会大会合同学術集会抄録集
    • Place of Presentation
      神戸
    • Year and Date
      2010-09-04
    • Related Report
      2011 Final Research Report
  • [Presentation] 小脳発達過程におけるフォークヘッドドメインを欠いた新規Foxp2アイソフォームの発現の解析2010

    • Author(s)
      田辺裕子
    • Organizer
      第33回日本神経科学大会・第53回日本神経科学会大会・第20回日本神経回路学会大会合同学術集会
    • Place of Presentation
      神戸コンベンションセンター(神戸)
    • Year and Date
      2010-09-04
    • Related Report
      2010 Annual Research Report
  • [Presentation] Ultrasonic vocalization of the knock-in mice with mutated Foxp2 related to speech-language disorder and normal Foxp2 expressed in Purkinje cells2009

    • Author(s)
      Fujita E、Tababe Y、Fujiwara Y、Mariko Momoi、Takashi Momoi
    • Organizer
      Neuroscience2009
    • Place of Presentation
      名古屋
    • Year and Date
      2009-09-18
    • Related Report
      2011 Final Research Report
  • [Presentation] Ultrasonic vocalization of the knock-in mice with mutated Foxp2 related to speech-language disorder and normal Foxp2 expressed in Purkinje cells2009

    • Author(s)
      Fujit E.
    • Organizer
      Neuroscience2009
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2009-09-18
    • Related Report
      2009 Annual Research Report

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Published: 2009-04-01   Modified: 2016-04-21  

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