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The roles of planar cell polarity in non-epithelial tissues

Research Project

Project/Area Number 26840075
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Developmental biology
Research InstitutionOsaka University (2015-2016)
Chiba University (2014)

Principal Investigator

HASHIMOTO Masakazu  大阪大学, 生命機能研究科, 助教 (60580496)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords平面内細胞極性 / 軟骨細胞 / 鼻 / 収斂伸長 / ゲノム編集 / 顔面形成
Outline of Final Research Achievements

We show that convergent extension- like cellular behavior in the nasal septum cartilage elongate the nasal process in proximodistal axis during the development of mice. While Wnt5a, a typical non- canonical Wnt ligand, is expressed in the distal tip of the nasal process, Prickle1, one of the planar cell polarity (PCP) core factor is expressed in the nasal cartilage. Mutant mice of these genes have short and wide snout as well as the deviated nasal septum due to the lack of the polarity of the chondrocyte of the nasal septum. Furthermore, the induced ubiquitous expression of Wnt5a also resulted in the nasal hypoplasia resulting from the chondrocyte polarity and orientation defects. These results suggest that the nasal cartilage senses the Wnt5a gradient along the proximodistal axis, and polarize the chondrocytes by a Prickle1-dependent manner for the convergent extension movement to form the long and thin nose in mammals.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (3 results)

All 2016 2015

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 2 results,  Acknowledgement Compliant: 1 results)

  • [Journal Article] Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse.2016

    • Author(s)
      Hashimoto M, Yamashita Y, Takemoto T.
    • Journal Title

      Developmental Biology

      Volume: 418 Issue: 1 Pages: 1-9

    • DOI

      10.1016/j.ydbio.2016.07.017

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Somatic cell reprogramming-free generation of genetically modified pigs.2016

    • Author(s)
      Tanihara F, Takemoto T, Kitagawa E, Rao S, Do LT, Onishi A, Yamashita Y, Kosugi C, Suzuki H, Sembon S, Suzuki S, Nakai M, Hashimoto M, Yasue A, Matsuhisa M, Noji S, Fujimura T, Fuchimoto D, Otoi T.
    • Journal Title

      Sci Adv

      Volume: 14 Issue: 9

    • DOI

      10.1126/sciadv.1600803

    • NAID

      120006240045

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Electroporation enables the efficient mRNA delivery into the mouse zygotes and facilitates CRISPR/Cas9-based genome editing.2015

    • Author(s)
      Hashimoto M. and Takemoto T.
    • Journal Title

      Scientific Reports

      Volume: 5 Issue: 1 Pages: 11315-11315

    • DOI

      10.1038/srep11315

    • NAID

      120006875680

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access

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Published: 2014-04-04   Modified: 2018-03-22  

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