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Molecular regulation of the developing commissural plate.

The Journal of comparative neurology | 2010

Coordinated transfer of information between the brain hemispheres is essential for function and occurs via three axonal commissures in the telencephalon: the corpus callosum (CC), hippocampal commissure (HC), and anterior commissure (AC). Commissural malformations occur in over 50 human congenital syndromes causing mild to severe cognitive impairment. Disruption of multiple commissures in some syndromes suggests that common mechanisms may underpin their development. Diffusion tensor magnetic resonance imaging revealed that forebrain commissures crossed the midline in a highly specific manner within an oblique plane of tissue, referred to as the commissural plate. This specific anatomical positioning suggests that correct patterning of the commissural plate may influence forebrain commissure formation. No analysis of the molecular specification of the commissural plate has been performed in any species; therefore, we utilized specific transcription factor markers to delineate the commissural plate and identify its various subdomains. We found that the mouse commissural plate consists of four domains and tested the hypothesis that disruption of these domains might affect commissure formation. Disruption of the dorsal domains occurred in strains with commissural defects such as Emx2 and Nfia knockout mice but commissural plate patterning was normal in other acallosal strains such as Satb2(-/-). Finally, we demonstrate an essential role for the morphogen Fgf8 in establishing the commissural plate at later developmental stages. The results demonstrate that correct patterning of the commissural plate is an important mechanism in forebrain commissure formation.

Pubmed ID: 20653027 RIS Download

Associated grants

  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-05
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-03
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES012665
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-02
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES012665-02
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-05
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-04
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES012665-03
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-08
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-09
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-02
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-04
  • Agency: NIBIB NIH HHS, United States
    Id: EB 003543
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES012665-01
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES012665-04
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-01
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-06
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543-01A1
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-06A1
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-07
  • Agency: NIBIB NIH HHS, United States
    Id: R01 EB003543
  • Agency: NIEHS NIH HHS, United States
    Id: ES 01266
  • Agency: NIA NIH HHS, United States
    Id: R01 AG020012-03
  • Agency: NIA NIH HHS, United States
    Id: AG 20012

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MRI Studio (tool)

RRID:SCR_001398

An image processing program running under Windows suitable for such tasks as tensor calculation, color mapping, fiber tracking, and 3D visualization. Most of operations can be done with only a few clicks. This tool evolved from DTI Studio. Tools in the program can be grouped in the following way: * Image Viewer * Diffusion Tensor Calculations * Fiber Tracking and Editing * 3D Visualization * Image File Management * Region of Interesting (ROI) Drawing and Statistics * Image Registration

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EMX1 (antibody)

RRID:AB_2314369

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NFIA antibody (antibody)

RRID:AB_2314931

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SIX3 (antibody)

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ZIC2 (antibody)

RRID:AB_2315623

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