PUBLICATION

Regulation of zebrafish melanocyte development by ligand-dependent BMP signaling

Authors
Gramann, A.K., Venkatesan, A.M., Guerin, M., Ceol, C.J.
ID
ZDB-PUB-191226-14
Date
2019
Source
eLIFE   8: (Journal)
Registered Authors
Ceol, Craig
Keywords
cancer biology, developmental biology, zebrafish
MeSH Terms
  • Animals
  • Bone Morphogenetic Proteins/antagonists & inhibitors
  • Bone Morphogenetic Proteins/genetics*
  • Cell Differentiation/genetics
  • Gene Expression Regulation, Developmental/genetics
  • Growth Differentiation Factor 6/genetics*
  • Humans
  • Ligands
  • Melanocytes/metabolism*
  • Melanocytes/pathology
  • Microphthalmia-Associated Transcription Factor/genetics*
  • Neoplasms/genetics
  • Neoplasms/pathology
  • Neural Crest/growth & development
  • Neural Crest/metabolism
  • Pigmentation/genetics
  • Signal Transduction/genetics
  • Zebrafish/genetics
  • Zebrafish/growth & development
  • Zebrafish Proteins/genetics*
PubMed
31868592 Full text @ Elife
Abstract
Preventing terminal differentiation is important in the development and progression of many cancers including melanoma. Recent identification of the BMP ligand GDF6 as a novel melanoma oncogene showed GDF6-activated BMP signaling suppresses differentiation of melanoma cells. Previous studies have identified roles for GDF6 orthologs during early embryonic and neural crest development, but have not identified direct regulation of melanocyte development by GDF6. Here, we investigate the BMP ligand gdf6a, a zebrafish ortholog of human GDF6, during the development of melanocytes from the neural crest. We establish that the loss of gdf6a or inhibition of BMP signaling during neural crest development disrupts normal pigment cell development, leading to an increase in the number of melanocytes and a corresponding decrease in iridophores, another neural crest-derived pigment cell type in zebrafish. This shift occurs as pigment cells arise from the neural crest and depends on mitfa, an ortholog of MITF, a key regulator of melanocyte development that is also targeted by oncogenic BMP signaling. Together, these results indicate that the oncogenic role ligand-dependent BMP signaling plays in suppressing differentiation in melanoma is a reiteration of its physiological roles during melanocyte development.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping