We have isolated and characterized mutations in Drosophila neurotactin
, a gene that encodes a cell adhesion protein widely expressed during
neural development. Analysis of both loss and gain of gene function co
nditions during embryonic and postembryonic development revealed speci
fic requirements for neurotactin during axon outgrowth, fasciculation,
and guidance. Furthermore, embryos of some double mutant combinations
of neurotactin and other genes encoding adhesion/signaling molecules,
including neuroglian, derailed, and kekkon1, displayed phenotypic syn
ergy. This result provides evidence for functional cooperativity in vi
vo between the adhesion and signaling pathways controlled by neorotact
in and the other three genes.