D e p a r t m e n t of Genetics, Iowa S t a t e U n i v e r s i t y , A m e s , Iowa 50010
ABSTRACTExperimental observations on mice support the hypothesis that the complete pigmentation of most normal mammals and birds develops by the expansion and inerger of clones of pigment cells from the same centers that appear as pigmented spots against a white background in piebald-spotted mutants. Specific piebald-spotted mutants, bt and s, having nearly normal pigment coverage in certain parts of their bodies were selected for progressive restriction of those areas until the center of each area was located. Repeated reversion of the same pigment areas in variegated Miw", Wa and V a heterozygotes indicated that each of the areas was a clone of cells derived from a single primordial melanoblast that migrated from the neural crest to the location of the center during embryogenesis. White regions completely separated cells of different clones into differently pigmented spots when piebald-spotting mutants, bt or s, were combined with vaiiegated Miwh/+. Because the separation of clones was so complete, it appears that no pigment cells exist in the intervening white regions at any stage of development. Additional evidence also indicates that restricted proliferation of pigment cells is a common end effect in all piebald-spotting mutants, even though more direct effects may be on the pigment cell, the neural crest or the tissue environment of the skin.