Imprecise excision has created a 3474bp deletion that removes from 51bp upstream of the insertion site of P{EPg}CortactinEPg35301 to 15bp downstream of the Cortactin gene.
Mutants show a weak border cell migration defect in the egg chamber.
Mutant border cells show a slightly reduced rate of uptake of the lipophilic dye FM4-64 compared to wild-type controls.
Homozygous mutants show no visible abnormalities. When mutant ovaries are examined, they exhibit a mild defect in 'dumping' - the transfer of bulk cytoplasmic material from nurse cells to the oocyte. The size of ring canals is seriously reduced in mutant ovaries. Eggs laid by mutant mothers were on average smaller than wild-type. The hatching rate of eggs from mutant mothers is also decreased. With low penetrance (about 6% of stages 5-9 egg chambers) mutants also display discontinuities in the follicular epithelium. Border cell migration is also delayed in mutant ovaries. This remains the case in ovaries with somatically mutant follicle cells but not in germ-line clones.
CortactinM7 has border follicle cell phenotype, suppressible by mimnull
CortactinM7 is a suppressor of border follicle cell phenotype of mimnull
mimnull CortactinM7 double mutants have a wild-type border cell migration phenotype in the egg chamber.