Dner inhibits neural progenitor proliferation and induces neuronal and glial differentiation in zebrafish

Fu Yu Hsieh, Tsu Lin Ma, Hung Yu Shih, Sheng Jia Lin, Ching Wen Huang, Hsiao Yun Wang, Yi Chuan Cheng*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

26 Scopus citations

Abstract

Delta/notch-like epidermal growth factor (EGF)-related receptor (DNER) is a single-pass transmembrane protein found to be a novel ligand in the Notch signaling pathway. Its function was previously characterized in the developing cerebellum and inner ear hair cells. In this study, we isolated a zebrafish homolog of DNER and showed that this gene is expressed in the developing nervous system. Overexpression of dner or the intracellular domain of dner was sufficient to inhibit the proliferation of neural progenitors and induce neuronal and glial differentiation. In contrast, the knockdown of endogenous Dner expression using antisense morpholino oligonucleotides increased the proliferation of neural progenitors and maintained neural cells in a progenitor status through inhibition of neuronal and glial differentiation. Through analysis of the antagonistic effect on the Delta ligand and the role of the potential downstream mediator Deltex1, we showed that Dner acts in Notch-dependent and Notch-independent manner. This is the first study to demonstrate a role for Dner in neural progenitors and neuronal differentiation and provides new insights into mediation of neuronal development and differentiation by the Notch signaling pathway.

Original languageEnglish
Pages (from-to)1-12
Number of pages12
JournalDevelopmental Biology
Volume375
Issue number1
DOIs
StatePublished - 01 03 2013

Keywords

  • Dner
  • Glial differentiation
  • Neural proliferation
  • Neuronal differentiation
  • Zebrafish

Fingerprint

Dive into the research topics of 'Dner inhibits neural progenitor proliferation and induces neuronal and glial differentiation in zebrafish'. Together they form a unique fingerprint.

Cite this