The mechanisms governing development of neural crest‐derived melanocytes, and how alterations in these pathways lead to hypopigmen‐tation disorders, are not completely understood. Hepatocyte growth factor/scatter factor (HGF/SF) signaling through the tyrosine‐kinase receptor, MET, is capable of promoting the proliferation, increasing the motility, and maintaining high tyrosinase activity and melanin synthesis of melanocytes in vitro. In addition, transgenic mice that ubiquitously overexpress HGF/SF demonstrate hyperpigmentation in the skin and leptomenigenes and develop melanomas. To investigate whether HGF/ SF‐MET signaling is involved in the development of neural crest‐derived melanocytes, transgenic embryos, ubiquitously overexpressing HGF/SF, were analyzed. In HGF/SF transgenic embryos, the distribution of melanoblasts along the characteristic migratory pathway was not affected. However, additional ectopically localized melanoblasts were also observed in the dorsal root ganglia and neural tube, as early as 11.5 days post coitus (p.c.). We utilized an in vitro neural crest culture assay to further explore the role of HGF/SF‐MET signaling in neural crest development. HGF/SF added to neural crest cultures increased melanoblast number, permitted differentiation into pigmented melanocytes, promoted melanoblast survival, and could replace mast‐cell growth factor/Steel factor (MGF) in explant cultures. To examine whether HGF/SF‐MET signaling is required for the proper development of melanocytes, embryos with a targeted Met null mutation (Met–/–) were analysed. In Met–/– embryos, melanoblast number and location were not overtly affected up to 14 days p.c. These results demonstrate that HGF/SF‐MET signaling influences, but is not required for, the initial development of neural crest‐derived melanocytes in vivo and in vitro.