The Drosophila tumor suppressor gene lethal (1) discs large (dlg) enco
des a protein necessary for normal cell growth in epithelial and brain
tissue. It shares high sequence identity to the mammalian synaptic pr
oteins PSD-95 and SAP-70, whose functions are unknown. To determine th
e localization and role of dig at synapses, we investigated its distri
bution and the effects of dig mutations on Drosophila neuromuscular ju
nctions. We show that dig immunoreactivity is expressed at one type of
glutamatergic synapse and is associated with both presynaptic and pos
tsynaptic membranes. Mutations in dig alter the expression of dig and
cause striking changes in the structure of the subsynaptic reticulum,
a postsynaptic specialization at these synapses. These results indicat
e that dig is required for normal synaptic structure and offer insight
s regarding the role of dig homologs at vertebrate synapses.