Identification of a rudimentary neural crest in a non-vertebrate chordate

Nature. 2012 Dec 6;492(7427):104-7. doi: 10.1038/nature11589. Epub 2012 Nov 7.

Abstract

Neural crest arises at the neural plate border, expresses a core set of regulatory genes and produces a diverse array of cell types, including ectomesenchyme derivatives that elaborate the vertebrate head. The evolution of neural crest has been proposed to be a key event leading to the appearance of new cell types that fostered the transition from filter feeding to active predation in ancestral vertebrates. However, the origin of neural crest remains controversial, as homologous cell types have not been unambiguously identified in non-vertebrate chordates. Here we show that the tunicate Ciona intestinalis possesses a cephalic melanocyte lineage (a9.49) similar to neural crest that can be reprogrammed into migrating 'ectomesenchyme' by the targeted misexpression of Twist (also known as twist-like 2). Our results suggest that the neural crest melanocyte regulatory network pre-dated the divergence of tunicates and vertebrates. We propose that the co-option of mesenchyme determinants, such as Twist, into the neural plate ectoderm was crucial to the emergence of the vertebrate 'new head'.

Publication types

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

MeSH terms

  • Animals
  • Cell Lineage
  • Cell Movement
  • Ciona intestinalis / anatomy & histology*
  • Ciona intestinalis / cytology
  • Ciona intestinalis / embryology*
  • Ciona intestinalis / genetics
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Gastrulation
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Limb Buds / embryology
  • Limb Buds / metabolism
  • Microphthalmia-Associated Transcription Factor / antagonists & inhibitors
  • Microphthalmia-Associated Transcription Factor / genetics
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Neural Crest / cytology
  • Neural Crest / embryology*
  • Neural Crest / metabolism
  • Neural Plate / cytology
  • Neural Plate / embryology
  • Neural Plate / metabolism
  • Phylogeny
  • Twist-Related Protein 1 / genetics
  • Twist-Related Protein 1 / metabolism
  • Wnt Signaling Pathway

Substances

  • Forkhead Transcription Factors
  • Microphthalmia-Associated Transcription Factor
  • Twist-Related Protein 1