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Related Experiment Video

Updated: Jun 30, 2026

Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders
07:40

Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders

Published on: April 14, 2017

How degrading: Cyp26s in hindbrain development.

Richard J White1, Thomas F Schilling

  • 1Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.

Developmental Dynamics : an Official Publication of the American Association of Anatomists
|September 26, 2008
PubMed
Summary
This summary is machine-generated.

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Retinoic acid (RA) is crucial for vertebrate development, patterning the hindbrain. Its spatial distribution is regulated by synthesis and degradation, with Cyp26 enzymes critical for forming RA gradients.

Area of Science:

  • Developmental biology
  • Molecular biology
  • Biochemistry

Background:

  • Retinoic acid (RA), a vitamin A derivative, is a key signaling molecule in vertebrate embryonic development.
  • RA is hypothesized to function as a morphogen, establishing the anterior-posterior axis patterning in the hindbrain.
  • Understanding RA's spatial distribution is essential for comprehending developmental patterning.

Purpose of the Study:

  • To investigate the regulatory mechanisms controlling the spatial distribution of retinoic acid during vertebrate development.
  • To elucidate the role of synthesis and degradation in establishing retinoic acid morphogen gradients.
  • To assess the contribution of Cyp26 enzymes in retinoic acid gradient formation and stability.

Main Methods:

  • Review of recent studies on retinoic acid regulation in various model systems.

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Last Updated: Jun 30, 2026

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Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders

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The Mouse Hindbrain As a Model for Studying Embryonic Neurogenesis

Published on: January 29, 2018

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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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  • Analysis of data on local synthesis and degradation of retinoic acid.
  • Incorporation of computational modeling to simulate retinoic acid gradient dynamics.
  • Main Results:

    • Local control of retinoic acid synthesis and degradation significantly influences its spatial distribution.
    • Computational models highlight the critical role of Cyp26 enzyme-mediated degradation in forming functional retinoic acid gradients.
    • Cyp26 activity is essential for maintaining gradient integrity despite fluctuations in retinoic acid levels.

    Conclusions:

    • The spatial distribution of retinoic acid is tightly regulated by localized synthesis and degradation processes.
    • Cyp26 enzymes are vital for establishing and maintaining retinoic acid morphogen gradients necessary for hindbrain patterning.
    • Understanding these regulatory mechanisms provides insights into developmental robustness and pattern formation.