Phototransduction in Drosophila occurs through the ubiquitous phosphoi
nositide-mediated signal transduction system. Major unresolved questio
ns in this pathway are the identity and role of the internal calcium s
tores in light excitation and the mechanism underlying regulation of C
a2+ release from internal stores. Treatment of Drosophila photorecepto
rs with ryanodine and caffeine disrupted the current induced by light,
whereas subsequent application of calcium-calmodulin (Ca-CaM) rescued
the inactivated photoresponse. In calcium-deprived wild-type Drosophi
la and in calmodulin-deficient transgenic flies, the current induced b
y light was disrupted by a specific inhibitor of Ca-CaM. Furthermore,
inhibition of Ca-CaM revealed light-induced release of calcium from in
tracellular stores. It appears that functional ryanodine-sensitive sto
res are essential for the photoresponse. Moreover, calcium release fro
m these stores appears to be a component of Drosophila phototransducti
on, and Ca-CaM regulates this process.