During Drosophila pupal metamorphosis, the motoneurons and muscles dif
ferentiate synchronously, providing an opportunity for extensive inter
cellular regulation during synapse formation. We examined the existenc
e of such interactions by developmentally delaying or permanently elim
inating synaptic partners during the formation of indirect flight musc
les. When we experimentally delayed muscle development, we found that
although adult-specific primary motoneuron branching still occurred, t
he higher order (synaptic) branching was suspended until the delayed m
uscle fibers reached a favourable developmental state. In reciprocal e
xperiments we found that denervation caused a decrease in the myoblast
pool. Furthermore, the formation of certain muscle fibers (dorsoventr
al muscles) was specifically blocked. Exceptions were the adult muscle
s that use larval muscle fibers as myoblast fusion targets (dorsal lon
gitudinal muscles), However, when these muscles were experimentally co
mpelled to develop without their larval precursors, they showed an abs
olute dependence on the motoneurons for their formation. These data sh
ow that the size of the myoblast pool and early events in fiber format
ion depend on the presence of the nerve, and that, conversely, periphe
ral arbor development and synaptogenesis is closely synchronized with
the developmental state of the muscle.