Hes5.9 Coordinate FGF and Notch Signaling to Modulate Gastrulation via Regulating Cell Fate Specification and Cell Migration in Xenopus tropicalis

Genes (Basel). 2020 Nov 18;11(11):1363. doi: 10.3390/genes11111363.

Abstract

Gastrulation drives the establishment of three germ layers and embryonic axes during frog embryonic development. Mesodermal cell fate specification and morphogenetic movements are vital factors coordinating gastrulation, which are regulated by numerous signaling pathways, such as the Wnt (Wingless/Integrated), Notch, and FGF (Fibroblast growth factor) pathways. However, the coordination of the Notch and FGF signaling pathways during gastrulation remains unclear. We identified a novel helix-loop-helix DNA binding domain gene (Hes5.9), which was regulated by the FGF and Notch signaling pathways during gastrulation. Furthermore, gain- and loss-of-function of Hes5.9 led to defective cell migration and disturbed the expression patterns of mesodermal and endodermal marker genes, thus interfering with gastrulation. Collectively, these results suggest that Hes5.9 plays a crucial role in cell fate decisions and cell migration during gastrulation, which is modulated by the FGF and Notch signaling pathways.

Keywords: FGF; Hes5.9; Notch; cell fate specification; cell migration; gastrulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Movement
  • Embryo, Nonmammalian / cytology*
  • Embryo, Nonmammalian / drug effects
  • Embryo, Nonmammalian / metabolism
  • Endoderm
  • Female
  • Fibroblast Growth Factors / metabolism*
  • Gastrulation / physiology
  • Gene Expression Regulation, Developmental
  • Mesoderm
  • Microinjections
  • Pyrroles / pharmacology
  • Receptors, Notch / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Xenopus / embryology*
  • Xenopus / metabolism
  • Xenopus Proteins / genetics*
  • Xenopus Proteins / metabolism

Substances

  • NOTCH1 protein, Xenopus
  • Pyrroles
  • Receptors, Notch
  • SU 5402
  • Transcription Factors
  • Xenopus Proteins
  • Fibroblast Growth Factors