We study the signaling and transcriptional interactions that lead to neural crest formation both at the tissue and the molecular level. Currently, we are applying gain- and loss-of-function approaches coupled transcriptome, regulatory analysis and bioinformatics to interrogate the molecular interactions that comprise a neural crest gene regulatory network (NC-GRN). We are also examining the role of epigenetic modifications in early in neural crest development and how they influence the NC-GRN.
The neural crest is a uniquely vertebrate innovation. We are cloning orthologues of neural crest and placode "marker genes" from a basal vertebrate (lamprey) and non-vertebrate chordate (amphioxus) as well as isolating regulatory regions for these markers. We are using loss-of-function approaches, transcriptome analysis and interspecific transplantation to dissect the basal NC-GRN and what may have driven evolution of jawed vertebrates.
Neural crest cells are among the most migratory cell type in vertebrate embryos. We are characterizing the machinery responsible for neural crest cell movement, the nature of the neural crest epithelial to mesenchymal transition to form a migratory cell type and the role of the migratory environment in influencing migratory pathway choices. A variety of cell labeling techniques, including DiI-labeling, microsurgical grafts and confocal time-lapse microscopy, are used to follow the pathways of neural crest migration in in a number of vertebrate species.
Neural crest cells are a highly multipotent cell type that gives rise to diverse derivatives including melanocytes, craniofacial skeleton and peripheral ganglia. Many of the cell types are prone to metastasis in the adult, forming melanomas, neuroblastomas, and other types of metastatic cancer. We are interested in comparing the mechanisms of neural crest invasive behavior with those causing adult neural crest derivatives to return to a migratory and invasive state.