An Eya1-Notch axis specifies bipotential epibranchial differentiation in mammalian craniofacial morphogenesis

Elife. 2017 Nov 15:6:e30126. doi: 10.7554/eLife.30126.

Abstract

Craniofacial morphogenesis requires proper development of pharyngeal arches and epibranchial placodes. We show that the epibranchial placodes, in addition to giving rise to cranial sensory neurons, generate a novel lineage-related non-neuronal cell population for mouse pharyngeal arch development. Eya1 is essential for the development of epibranchial placodes and proximal pharyngeal arches. We identify an Eya1-Notch regulatory axis that specifies both the neuronal and non-neuronal commitment of the epibranchial placode, where Notch acts downstream of Eya1 and promotes the non-neuronal cell fate. Notch is regulated by the threonine phosphatase activity of Eya1. Eya1 dephosphorylates p-threonine-2122 of the Notch1 intracellular domain (Notch1 ICD), which increases the stability of Notch1 ICD and maintains Notch signaling activity in the non-neuronal epibranchial placodal cells. Our data unveil a more complex differentiation program in epibranchial placodes and an important role for the Eya1-Notch axis in craniofacial morphogenesis.

Keywords: Eya1 phosphatase; Notch; developmental biology; epibranchial placode; mouse; pharyngeal arch; pharyngeal epithelium; stem cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Branchial Region / embryology*
  • Cell Differentiation
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Morphogenesis*
  • Nuclear Proteins / metabolism*
  • Protein Tyrosine Phosphatases / metabolism*
  • Receptor, Notch1 / metabolism*
  • Signal Transduction*

Substances

  • Intracellular Signaling Peptides and Proteins
  • Notch1 protein, mouse
  • Nuclear Proteins
  • Receptor, Notch1
  • Eya1 protein, mouse
  • Protein Tyrosine Phosphatases