Regulation of zebrafish melanocyte development by ligand-dependent BMP signaling
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.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Dec 23, 2019
- Source ID
- 10.7554/elife.50047
Entities
People
- Alec K Gramann
- Arvind M. Venkatesan
- Craig J Ceol
- Melissa Guerin
Organizations
- Congressionally Directed Medical Research Programs
- Melanoma Research Foundation
- National Cancer Institute
- National Center for Advancing Translational Sciences
- National Institute of Arthritis and Musculoskeletal and Skin Diseases
- Sidney Kimmel Foundation
- University of Massachusetts Medical School