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2018 年度 実施状況報告書

Unravelling Mechanisms Underlying Termination of Neuronal Migration

研究課題

研究課題/領域番号 16K07010
研究機関国立遺伝学研究所

研究代表者

ZHU YAN  国立遺伝学研究所, 遺伝形質研究系, 助教 (50464235)

研究期間 (年度) 2016-04-01 – 2020-03-31
キーワードneuronal migration / termination of migration / RNA-seq / Tag-1 / Bace1
研究実績の概要

To understand how termination of neuronal migration is controlled, we performed: (1) RNA-seq based transcriptome profiling, and (2) examining the function and down-regulation of Tag-1. During this fiscal year, we performed gain- and loss-of-functional screening of candidate genes selected from RNA-seq, which uncovered several molecules in the process of termination. For approach (2), we discovered that Tag-1 can be processed by a beta-secretase 1 (Bace1). We showed that in vivo, Bace1 appears to regulate the Tag-1 protein level. A Bace1 resistant Tag-1 mutant prevents neurons from entering their termination sites.

現在までの達成度 (区分)
現在までの達成度 (区分)

2: おおむね順調に進展している

理由

(1) Our RNA-seq experiment has generated rich molecular information, from which we have identified the involvement of a few molecules in termination of neuronal migration via functional screenings. Although there are further details to be worked out for these molecules, I believe we have reached the goal initially set by this grant.

(2) In the second candidate molecule approach, we have focused on Tag-1. We have demonstrated that Tag-1 plays an important role in maintaining chain migration of neurons and in preventing neurons from leaving their migratory stream prematurely. We further uncovered a role of a beta-secretase, Bace1, in processing Tag-1, which may contribute to its down-regulation prior to termination of migration.

今後の研究の推進方策

Termination of neuronal migration is a multi-step process involving detachment from migratory stream, change of migratory polarity, and cessation of motility. Both our RNA-seq and Tag-1 projects have given us a molecular glimpse into these steps. However, the trigger that initiate the termination of migration is still unknown. A future line of research would be to probe into the nature of this trigger, in respect of which I would like to address several fundamental questions: (1) is the timing of migration termination merely controlled by extrinsic cues or to some extent an internal clock; (2) how is the termination of migration coupled with initiation of neuronal maturation. The datasets from our RNA-seq experiment may hold the clues and provide the tools to address these questions.

次年度使用額が生じた理由

We have obtained a large amount of molecular information in this project. Although we have so far identified several molecules, we are still working on molecular details of their mechanisms in order to submit our study for publication. The incurring amount will be used to cover the costs of these experiments as well as paying for technical support.

  • 研究成果

    (3件)

すべて 2019 2018

すべて 学会発表 (3件) (うち国際学会 1件)

  • [学会発表] Mechanisms underlying termination of tangential neuronal migration investigated by a RNA-seq based approach2019

    • 著者名/発表者名
      Masuda A, Nakaoka H, Toyoda A, Hirata T, Zhu Y
    • 学会等名
      Spring Meeting of the Japanese Society of genetics, Mishima
  • [学会発表] Mechanisms underlying termination of tangential neuronal migration investigated by a RNA-seq based approach2018

    • 著者名/発表者名
      Masuda A, Nakaoka H, Toyoda A, Hirata T, Zhu Y
    • 学会等名
      Biennial Meeting of the International Society for Developmental Neuroscience, Nara
    • 国際学会
  • [学会発表] Mechanisms underlying termination of tangential neuronal migration investigated by a RNA-seq based approach2018

    • 著者名/発表者名
      Masuda A, Nakaoka H, Toyoda A, Hirata T, Zhu Y
    • 学会等名
      Annual Meeting of the Japanese Society of Neurosience, Kobe

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公開日: 2019-12-27  

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