The garnet gene was one of the first genes to be identified in Drosophila m
elanogaster. Mutations in the garnet gene affect both of the biochemically
distinct types of pigments in the eye and disrupt pigmentation of other org
ans. As an initial step in the analysis of this gene, we have analyzed the
pigmentation defects in several of the garnet alleles. We have also cloned
the gene and examined its expression in various tissues and at different st
ages of development. The garnet gene is expressed throughout development an
d in all tissues examined. Structurally related sequences can be detected i
n a variety of other eukaryotes. The predicted protein sequence of the garn
et product resembles clathrin and nonclathrin adaptin proteins and is highl
y similar to the delta subunit of the newly isolated mammalian AP-3 adaptin
complex, which is associated with the trans-Golgi network and endosomes. T
his suggests that garnet encodes a protein that acts in the intracellular s
orting and trafficking of vesicles from the trans-Golgi network to endosome
s, and related specialized organelles such as the pigment granule. This fin
ding provides an explanation for the phenotype of garnet mutations and pred
icts that other Drosophila eye-colour genes will be a rich resource for the
genetic dissection of intracellular vesicle transport.