A dual function of FGF signaling in Xenopus left-right axis formation

Development. 2019 May 10;146(9):dev173575. doi: 10.1242/dev.173575.

Abstract

Organ left-right (LR) asymmetry is a conserved vertebrate feature, which is regulated by left-sided activation of Nodal signaling. Nodal asymmetry is established by a leftward fluid-flow generated at the ciliated LR organizer (LRO). Although the role of fibroblast growth factor (FGF) signaling pathways during mesoderm development is conserved, diverging results from different model organisms suggest a non-conserved function in LR asymmetry. Here, we demonstrate that FGF is required during gastrulation in a dual function at consecutive stages of Xenopus embryonic development. In the early gastrula, FGF is necessary for LRO precursor induction, acting in parallel with FGF-mediated mesoderm induction. During late gastrulation, the FGF/Ca2+-branch is required for specification of the flow-sensing lateral LRO cells, a function related to FGF-mediated mesoderm morphogenesis. This second function in addition requires input from the calcium channel Polycystin-2. Thus, analogous to mesoderm development, FGF activity is required in a dual role for laterality specification; namely, for generating and sensing leftward flow. Moreover, our findings in Xenopus demonstrate that FGF functions in LR development share more conserved features across vertebrate species than previously anticipated.

Keywords: FGF; LRO; Left-right asymmetry; Leftward flow; Pkd2; Sprouty.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / genetics
  • Body Patterning / physiology
  • Cilia / metabolism
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism*
  • Forkhead Transcription Factors / metabolism
  • Gastrula / metabolism
  • Gastrulation / physiology
  • Mesoderm / metabolism
  • Signal Transduction / physiology
  • TRPP Cation Channels / metabolism
  • Xenopus Proteins / metabolism
  • Xenopus laevis

Substances

  • FOXJ1 protein, Xenopus
  • Forkhead Transcription Factors
  • TRPP Cation Channels
  • Xenopus Proteins
  • polycystic kidney disease 2 protein
  • Fibroblast Growth Factors