During development of the Drosophila peripheral nervous system, different proneural genes encoding basic helix-loop-helix transcription factors are required for different sensory organs to form. atonal (ato) is the proneural gene required for chordotonal organs and R8 photoreceptors, whereas the achaete-scute complex contains proneural genes for external sensory organs such as the macrochaetae, large sensory bristles. Whereas ectopic ato expression induces chordotonal organ formation, ectopic scute expression produces external sensory organs but not chordotonal organs in the wing. Proneural genes thus appear to specify the sensory organ type. In the ommatidium, or unit eye, R8 is the first photoreceptor to form and appears to recruit other photoreceptors and support cells. In the atonal 1 (ato 1 ) mutant, R8 photoreceptors fail to form, thereby resulting in the complete absence of ommatidia. To our surprise, we found that ectopic scute expression in the ato 1 mutant induces the formation of ommatidia, which occasionally sprout ectopic macrochaetae. Remarkably, many scute-induced ommatidia lack R8 although they contain outer photoreceptors. N eural precursors for sensory organs in Drosophila are specified by proneural genes, which are first expressed in clusters of equipotent cells, the proneural clusters, and then restricted to the cells singled out from these proneural clusters to become neural precursors (1-7). Different proneural genes, which code for transcriptional regulators with the basic helix-loop-helix motif, are required for the formation of neural precursors for different sensory organs. For example, the proneural gene atonal (ato) is required for the formation of photoreceptors (4) and chordotonal organs, which are stretch receptors or auditory sensors (3). The proneural genes in the achaete-scute complex, on the other hand, are necessary for the formation of external sensory organs, bristles that are sensitive to physical or chemical stimuli (2).The proneural genes appear to be capable of specifying the type of neural precursor they induce, even though their expression in the proneural clusters depends on positional information, which in principle may specify the type of neural precursors that emerge from these proneural clusters. For example, ectopic expression of scute results in the formation of external sensory organs exclusively (3,8,10) and cannot rescue the chordotonal organ defect in the ato 1 mutant (8). In the central nervous system, ectopic expression of achaete or scute, but not ato, can restore MP2 precursors of mutants lacking these precursors (11,12). Only ato is capable of promoting ectopic chordotonal organ formation (3,8,9); its ectopic expression can even convert external sensory organs into chordotonal organs (9). Like chordotonal organs, photoreceptors normally depend on ato for their formation (4). It is thus of interest to determine whether photoreceptors can be induced only by ectopic expression of ato.Drosophila eye morphogenesis begins at the posterior tip of the eye imagi...