Expression of Ras85DQ13.hs using heat shock results in a high frequency of defects in the dorsal cuticle.
Expression in the embryo inhibits, to large extent, naturally occurring cell death. Apoptosis only remains in the CNS.
Partial rescue of tracheal migration defect in btl homozygotes.
One copy of the P{hs-Ras1Q13} construct causes a low hatching rate. Some unhatched embryos display a range of abdominal defects and duplicated filzkorper material. Other display defects in head involution, germband retraction or dorsal/ventral patterning.
Ras85DQ13.hs has border follicle cell phenotype, suppressible by slboUAS.cLa/Scer\GAL4hs.PB
Border cell migration defect is rescued by Scer\GAL4hs.PB-mediated expression of slboScer\UAS.cLa.