A morphogen gradient of Wnt/beta-catenin signalling regulates anteroposterior neural patterning in Xenopus

Development. 2001 Nov;128(21):4189-201. doi: 10.1242/dev.128.21.4189.

Abstract

Anteroposterior (AP) patterning of the vertebrate neural plate is initiated during gastrulation and is regulated by Spemann's organizer and its derivatives. The prevailing model for AP patterning predicts a caudally increasing gradient of a 'transformer' which posteriorizes anteriorly specified neural cells. However, the molecular identity of the transforming gradient has remained elusive. We show that in Xenopus embryos (1) dose-dependent Wnt signalling is both necessary and sufficient for AP patterning of the neuraxis, (2) Wnt/beta-catenin signalling occurs in a direct and long-range fashion within the ectoderm, and (3) that there is an endogenous AP gradient of Wnt/beta-catenin signalling in the presumptive neural plate of the Xenopus gastrula. Our results indicate that an activity gradient of Wnt/beta-catenin signalling acts as transforming morphogen to pattern the Xenopus central nervous system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Early Growth Response Protein 2
  • Ectoderm / metabolism
  • Embryo, Nonmammalian
  • Female
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nervous System / embryology*
  • Nervous System / metabolism
  • Otx Transcription Factors
  • Proteins / genetics
  • Proteins / metabolism
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Signal Transduction*
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Wnt Proteins
  • Wnt3 Protein
  • Xenopus / embryology*
  • Xenopus / genetics
  • Xenopus / metabolism
  • Xenopus Proteins
  • Zebrafish Proteins*
  • beta Catenin

Substances

  • CTNNB1 protein, Xenopus
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • Early Growth Response Protein 2
  • Homeodomain Proteins
  • Nerve Tissue Proteins
  • Otx Transcription Factors
  • Proteins
  • Proto-Oncogene Proteins
  • Trans-Activators
  • Transcription Factors
  • Wnt Proteins
  • Wnt3 Protein
  • Xenopus Proteins
  • Zebrafish Proteins
  • beta Catenin