Sonic hedgehog regulation of Foxf2 promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis

Development. 2017 Jun 1;144(11):2082-2091. doi: 10.1242/dev.149930. Epub 2017 May 15.

Abstract

Cleft lip is one of the most common human birth defects, yet our understanding of the mechanisms that regulate lip morphogenesis is limited. Here, we show in mice that sonic hedgehog (Shh)-induced proliferation of cranial neural crest cell (cNCC) mesenchyme is required for upper lip closure. Gene expression profiling revealed a subset of Forkhead box (Fox) genes that are regulated by Shh signaling during lip morphogenesis. During cleft pathogenesis, reduced proliferation in the medial nasal process mesenchyme paralleled the domain of reduced Foxf2 and Gli1 expression. SHH ligand induction of Foxf2 expression was dependent upon Shh pathway effectors in cNCCs, while a functional GLI-binding site was identified downstream of Foxf2 Consistent with the cellular mechanism demonstrated for cleft lip pathogenesis, we found that either SHH ligand addition or FOXF2 overexpression is sufficient to induce cNCC proliferation. Finally, analysis of a large multi-ethnic human population with cleft lip identified clusters of single-nucleotide polymorphisms in FOXF2 These data suggest that direct targeting of Foxf2 by Shh signaling drives cNCC mesenchyme proliferation during upper lip morphogenesis, and that disruption of this sequence results in cleft lip.

Keywords: Cleft lip; Cranial neural crest cell; Forkhead box; Human; Medial nasal process; Mouse; Orofacial morphogenesis; Sonic hedgehog.

MeSH terms

  • Animals
  • Binding Sites
  • Cell Proliferation
  • Cleft Lip / genetics*
  • Cleft Lip / pathology
  • Down-Regulation / genetics
  • Ethnicity / genetics
  • Forkhead Transcription Factors / genetics*
  • Forkhead Transcription Factors / metabolism
  • Gene Expression Regulation, Developmental
  • Genetic Association Studies
  • Genetic Loci
  • Hedgehog Proteins / metabolism*
  • Humans
  • Lip / embryology
  • Lip / metabolism
  • Mesoderm / metabolism
  • Mesoderm / pathology*
  • Mice, Inbred C57BL
  • Morphogenesis / genetics*
  • Neural Crest / pathology*
  • Polymorphism, Single Nucleotide / genetics
  • Signal Transduction / genetics
  • Skull / pathology*

Substances

  • FOXF2 protein, human
  • Forkhead Transcription Factors
  • Foxf2 protein, mouse
  • Hedgehog Proteins
  • Shh protein, mouse