Neurogenic gene regulatory pathways in the sea urchin embryo

Development. 2016 Jan 15;143(2):298-305. doi: 10.1242/dev.125989. Epub 2015 Dec 10.

Abstract

During embryogenesis the sea urchin early pluteus larva differentiates 40-50 neurons marked by expression of the pan-neural marker synaptotagmin B (SynB) that are distributed along the ciliary band, in the apical plate and pharyngeal endoderm, and 4-6 serotonergic neurons that are confined to the apical plate. Development of all neurons has been shown to depend on the function of Six3. Using a combination of molecular screens and tests of gene function by morpholino-mediated knockdown, we identified SoxC and Brn1/2/4, which function sequentially in the neurogenic regulatory pathway and are also required for the differentiation of all neurons. Misexpression of Brn1/2/4 at low dose caused an increase in the number of serotonin-expressing cells and at higher dose converted most of the embryo to a neurogenic epithelial sphere expressing the Hnf6 ciliary band marker. A third factor, Z167, was shown to work downstream of the Six3 and SoxC core factors and to define a branch specific for the differentiation of serotonergic neurons. These results provide a framework for building a gene regulatory network for neurogenesis in the sea urchin embryo.

Keywords: Brn1/2/4; Embryogenesis; Neurogenesis; Sea urchin; Six3; SoxC; Strongylocentrotus purpuratus.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Body Patterning / genetics
  • Body Patterning / physiology
  • Embryo, Nonmammalian / cytology
  • Embryo, Nonmammalian / metabolism*
  • Eye Proteins / genetics
  • Eye Proteins / metabolism
  • Gene Expression Regulation, Developmental
  • Homeobox Protein SIX3
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • POU Domain Factors / genetics
  • POU Domain Factors / metabolism
  • Sea Urchins / embryology*
  • Sea Urchins / metabolism*

Substances

  • Eye Proteins
  • Homeodomain Proteins
  • Nerve Tissue Proteins
  • POU Domain Factors
  • transcription factor Brn-2
  • Pou3f3 protein, mouse