The photoreceptor neurons (R cells) of the Drosophila compound eye ela
borate a precise array of neuronal connections in the brain. These pro
jections exhibit target specificity and create topographic maps (retin
otopy). We have screened histologically for mutations disrupting R cel
l connectivity in developing tissue. Eighty mutations were isolated fr
om over 6000 ethylmethane sulfonate-mutagenized lines. Characterizatio
n of these mutations included genetic mosaic analysis to determine whe
ther the gene is required in the retina or in the optic ganglia. Most
mutations were found to affect connectivity indirectly by disrupting d
evelopment more generally in the eye or brain. Genes were identified a
s candidates for playing direct roles in R cell connectivity by affect
ing axonal outgrowth (eddy), target recognition (limbo and nonstop), a
nd retinotopy (limbo).