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Nuclear lamina targeting is a timing mechanism for dendrite outgrowth

Publicly Offered Research

Project AreaInterplay of developmental clock and extracellular environment in brain formation
Project/Area Number 17H05780
Research Category

Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

Allocation TypeSingle-year Grants
Review Section Biological Sciences
Research InstitutionInstitute of Physical and Chemical Research

Principal Investigator

Moore Adrian  国立研究開発法人理化学研究所, 脳神経科学研究センター, チームリーダー (30442932)

Project Period (FY) 2017-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥10,400,000 (Direct Cost: ¥8,000,000、Indirect Cost: ¥2,400,000)
Fiscal Year 2018: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2017: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Keywordsdendrite / time / imaging / neuron / differentiation / lamina / chromatin / cytoskeleton
Outline of Annual Research Achievements

We use Drosophila somatosensory (nociceptive and mechanosensory) neurons as an experimental model because they form arrays of related neuron types that nonetheless exhibit neuron type-specific differences in dendrite arbor pattern, axonal projection, and sensory channel content. This organization has enabled us to identify and examine molecular processes that generate differences between neuron types. During all stages of dendrite arbor outgrowth there is extensive and continual remodeling. Hidden within this background is a subset of specific events critical for setting arbor structure; to identify them requires prolonged live imaging and the subsequent linking of specific cell behaviors to final pattern outcomes. We reasoned that such systematic analyses require quantification of large temporal series of neuron structure data, and we adapted recent technological advances in automation of tracing and feature detection to enable this. We carried out in vivo time-lapse imaging of Drosophila c4da differentiation with machine learning based quantification of arbor patterning, and with molecular-level tracking of cytoskeletal remodeling. Overall, our analysis revealed that Myo6 and the transcription factor Knot regulate transient surges of microtubule polymerization at dendrite tips; they drive retrograde extension of an actin filament array that specifies anterograde microtubule polymerization and guides these microtubules to subdivide the tip into multiple branches. We find this tunable branching mechanism is key to define and diversify dendrite arbor compartmentalization.

Research Progress Status

平成30年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

平成30年度が最終年度であるため、記入しない。

Report

(2 results)
  • 2018 Annual Research Report
  • 2017 Annual Research Report
  • Research Products

    (10 results)

All 2019 2018 2017 Other

All Int'l Joint Research (1 results) Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results) Presentation (8 results) (of which Int'l Joint Research: 5 results,  Invited: 6 results)

  • [Int'l Joint Research] Brandeis University(米国)

    • Related Report
      2017 Annual Research Report
  • [Journal Article] Stages and transitions in dendrite arbor differentiation.2019

    • Author(s)
      Yoong LF, Pai YJ, Moore AW
    • Journal Title

      Neurosci Res

      Volume: 138 Pages: 70-78

    • DOI

      10.1016/j.neures.2018.09.015

    • Related Report
      2018 Annual Research Report
    • Peer Reviewed / Int'l Joint Research
  • [Presentation] Atypical myosin tunes the level of dendrite arbor subdivision2019

    • Author(s)
      Yoong LF
    • Organizer
      2nd Asia pacific Neurobiology of Drosophila
    • Related Report
      2018 Annual Research Report
    • Invited
  • [Presentation] Atypical myosin tunes the level of dendrite arbor subdivision2018

    • Author(s)
      Moore AW
    • Organizer
      Europoean Neurobiology of Drosophila
    • Related Report
      2018 Annual Research Report
    • Invited
  • [Presentation] Atypical myosin tunes the level of dendrite arbor subdivision2018

    • Author(s)
      Yoong LF
    • Organizer
      15th Meeting of the Asian-Pacific Society for Neurochemistry
    • Related Report
      2018 Annual Research Report
    • Invited
  • [Presentation] Defining and Diversifying Dendrite Arbor Topology2018

    • Author(s)
      Adrian Moore
    • Organizer
      EMBO Workshop on Neural Development
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] Blink and you will miss it: an in vivo time-lapse imaging screen, coupled with automated dendrite feature detection and quantification, reveals the molecular mechanisms of major dendrite branch formation2017

    • Author(s)
      Li Foong Yoong and Adrian Moore
    • Organizer
      Neurobiology of Drosophila
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Major Branches in the Dendrite Arbor Arise by Stabilization of Single Actin Bundles at the Dendrite Tip2017

    • Author(s)
      Adrian Moore
    • Organizer
      Asia-Pacific Drosophila Neurobiology Conference
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] Important things have small beginnings: Major branches in the dendrite arbor arise by stabilization of single actin bundles at the dendrite tip.2017

    • Author(s)
      Adrian Moore
    • Organizer
      EMBO Conference on Cell Biology of the Neuron: Polarity, Plasticity and Regeneration
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] Tunable Targeting of Polymerizing Dendritic Microtubules Determines Arbor Topology2017

    • Author(s)
      Adrian Moore
    • Organizer
      IUBMB Focused Meeting on Emerging Concepts of the Neuronal Cytoskeleton
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research / Invited

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Published: 2017-04-28   Modified: 2022-06-09  

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