fog4, foghkb.PB exhibit motor axon defects in late stage 16 embryos, with particular problems in SNa bifurcation.
fog4, foghkb.PB mutants display defects in SNa motor axon guidance. In most segments that display a phenotype, either the posterior or the anterior SNa branch is missing. Occasionally, extra anterior branches are observed. In rare cases, the entire SNa appears to stall at the bifurcation point.
Embryos carrying foghkb.PB show a transient depression in the dorsal head region. The surfaces of the cells in this region show membrane blebbing and constrictions closely resembling those seen in cells along the ventral furrow of wild-type embryos. The nuclei of these cells have migrated from an apical to a basal location.
foghkb.PB has embryonic head | dorsal phenotype, suppressible by RhoGEF21.1
foghkb.PB has embryonic head | dorsal phenotype, suppressible by RhoGEF24.1
The depression in the dorsal head region is not seen in embryos carrying foghkb.PB which are derived from homozygous RhoGEF21.1 or RhoGEF24.1 female germline clones.