Mutations at the W locus affect survival of neural crest-derived melanocytes in the mouse

J Cable, IJ Jackson, KP Steel - Mechanisms of development, 1995 - Elsevier
J Cable, IJ Jackson, KP Steel
Mechanisms of development, 1995Elsevier
The development of melanoblasts in normally pigmented and dominant spotting (W)
embryos was followed by in situ hybridisation to TRP-2/DT mRNA, which labels migratory
melanoblasts from 10 days post coitum. Numerous melanoblasts migrate to the inner ear
around 11 days. In contrast, few migratory melanoblasts are associated with the eye or skin
at this stage and melanoblast distribution within the trunk and tail is patchy. The distribution
of melanoblasts in 10.5–11-day-old W vW v, W shW sh and W 41W 41 mutants was similar …
The development of melanoblasts in normally pigmented and dominant spotting (W) embryos was followed by in situ hybridisation to TRP-2/DT mRNA, which labels migratory melanoblasts from 10 days post coitum. Numerous melanoblasts migrate to the inner ear around 11 days. In contrast, few migratory melanoblasts are associated with the eye or skin at this stage and melanoblast distribution within the trunk and tail is patchy. The distribution of melanoblasts in 10.5–11-day-old W vW v, W shW sh and W 41W 41 mutants was similar to that in controls but melanoblast density was lower and by 12 days was severely reduced. These results suggest that mutations of the c-kit receptor tyrosine kinase encoded at the W locus do not alter early migration or differentiation of melanoblasts but severely affect melanoblast survival.
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