We have examined the role of innervation in directing embryonic myogen
esis, using a mutant (prospero), which delays the pioneering of periph
eral motor nerves of the Drosophila embryo. In the absence of motor ne
rves, myoblasts fuse normally to form syncytial myotubes, myotubes for
m normal attachments to the epidermis, and a larval musculature compar
able to the wild-type pattern is generated and maintained. Likewise, t
he twist-expressing myoblasts that prefigure the adult musculature seg
regate normally in the absence of motor nerves, migrate to their final
embryonic positions and continue to express twist until the end of em
bryonic development. In the absence of motor nerves, myotubes uncouple
at the correct developmental stage to form single cells. Subsequently
, uninnervated myotubes develop the mature electrical and contractile
properties of larval muscles with a time course indistinguishable from
normally innervated myotubes. We conclude that innervation plays no r
ole in the patterning, morphogenesis, maintenance or physiological dev
elopment of the somatic muscles in the Drosophila embryo.