Wnt, Ptk7, and FGFRL expression gradients control trunk positional identity in planarian regeneration

Elife. 2016 Apr 13:5:e12850. doi: 10.7554/eLife.12850.

Abstract

Mechanisms enabling positional identity re-establishment are likely critical for tissue regeneration. Planarians use Wnt/beta-catenin signaling to polarize the termini of their anteroposterior axis, but little is known about how regeneration signaling restores regionalization along body or organ axes. We identify three genes expressed constitutively in overlapping body-wide transcriptional gradients that control trunk-tail positional identity in regeneration. ptk7 encodes a trunk-expressed kinase-dead Wnt co-receptor, wntP-2 encodes a posterior-expressed Wnt ligand, and ndl-3 encodes an anterior-expressed homolog of conserved FGFRL/nou-darake decoy receptors. ptk7 and wntP-2 maintain and allow appropriate regeneration of trunk tissue position independently of canonical Wnt signaling and with suppression of ndl-3 expression in the posterior. These results suggest that restoration of regional identity in regeneration involves the interpretation and re-establishment of axis-wide transcriptional gradients of signaling molecules.

Keywords: S. mediterranea; Wnt; axis; developmental biology; pattern control; planaria; regeneration; stem cells.

Publication types

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

MeSH terms

  • Animals
  • Body Patterning / genetics*
  • Cell Differentiation
  • Gene Expression Regulation*
  • Helminth Proteins / genetics*
  • Helminth Proteins / metabolism
  • Planarians / genetics*
  • Planarians / metabolism
  • Planarians / ultrastructure
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptors, Fibroblast Growth Factor / genetics*
  • Receptors, Fibroblast Growth Factor / metabolism
  • Receptors, Wnt / genetics
  • Receptors, Wnt / metabolism
  • Regeneration / genetics
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription, Genetic
  • Wnt Proteins / genetics*
  • Wnt Proteins / metabolism
  • Wnt Signaling Pathway
  • beta Catenin / genetics
  • beta Catenin / metabolism

Substances

  • Helminth Proteins
  • Receptors, Fibroblast Growth Factor
  • Receptors, Wnt
  • Wnt Proteins
  • beta Catenin
  • Receptor Protein-Tyrosine Kinases