Expression of Egfr1.Scer\UAS under the control of Scer\GAL4esg-NP5130 (restricted to the adult stages using Scer\GAL80ts.αTub84B) results in an increase in intestinal stem cell division.
The number of cells posterior to the furrow in eye discs that display caspase activation is reduced in Egfr1.Scer\UAS; Scer\GAL4GMR.PF animals (Note: this effect is less dramatic than that seen with Egfr2.Scer\UAS). There is no accompanying increase in the levels of photoreceptor differentiation at this stage, but there is an increase in mitosis during the second mitotic wave (G2 to M progression, posterior to the furrow). The number of cells displaying caspase activation in pupal eye discs at 30 hours after puparium formation, is also significantly reduced in these animals, accompanied by significantly increased photoreceptor differentiation.
Expression of Egfr1.Scer\UAS under the control of Scer\GAL4GMR.PF results in division of all second mitotic wave cells in the eye. There is an increase in the mitotic index and mitoses are shifted more anteriorly. There is no increase in photoreceptor differentiation.
When expression is driven by Scer\GAL432B there is no effect on wing development. When expression is driven by Scer\GAL4h-H10 there is no effect on eye development.
Egfr1.UAS, Scer\GAL4NP5130 has intestinal stem cell | adult stage phenotype, non-suppressible by mir-bansponge.UAS.DsRed(Unk), Scer\GAL4NP5130
Expression of bansponge.Scer\UAS.T:Disc\RFP does not suppress the increase in intestinal stem cell division when Egfr1.Scer\UAS is expressed under the control of Scer\GAL4esg-NP5130 (restricted to the adult stages using Scer\GAL80ts.αTub84B).
Expression of Egfr1.Scer\UAS under the control of Scer\GAL4GMR.PF in EgfrE3 flies results in mitosis in all cells in the eye disc.
Carried in plasmid " pUAST:dEGFR1 " and transfected into S3 cells.
Carried in a plasmid, transfected into S3 cells and used in co-immunoprecipitation assays.