AI Article Synopsis

  • Radial glia cells are essential for neuronal migration and as sources of neural progenitor cells during central nervous system development.
  • Notch signaling has been shown to promote the formation of radial glia cells, but the complete mechanism of this signaling process has not yet been fully understood.
  • The study identifies Oct-1, a POU transcription factor, as a key downstream target of Notch signaling, which is crucial for radial glia formation in the developing brain.

Article Abstract

Radial glia cells function as guide cells for neuronal migration and a source of neural progenitor cells, and play a crucial role for the development of the central nervous system. To date, several signals have been demonstrated to promote the formation of radial glia cells and Notch signaling is one such signal. However, the mechanism of the signaling hierarchy of radial glia developmental cascade promoted by Notch signaling still remains incomplete. Here we show that Notch signaling promotes Xenopus radial glia formation and that the Notch activation is sufficient for radial glia formation prior to neural tube closure. Moreover, we have identified Oct-1 (POU2f1), a POU transcription factor, as a downstream target of Notch signaling by microarray based screen. We demonstrate that the expression of Oct-1 in the brain is regulated by Notch signaling and that Oct-1 is sufficient and necessary for radial glia formation. Together, Oct-1 is a downstream effector of Notch signaling during radial glia formation.

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Source
http://dx.doi.org/10.1016/j.ydbio.2007.12.013DOI Listing

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