Over-expression of Egfr1.A887T.Scer\UAS in MARCM mutant clones (under the control of Scer\GAL4esg-NP5130) induces intestinal stem cell proliferation.
Over-expression using Scer\GAL4fkh.PH leads to invagination of salivary gland cells with slightly aberrant shapes and to an invagination hole that is too large. This leads to fully invaginated glands with a too large and aberrantly shaped lumen, although the individual and common ducts appear normal.
Expression of Egfr1.A887T.Scer\UAS under the control of Scer\GAL4dpp.blk1 results in ectopic marginal furrow formation in the eye disc.
When expression is driven by Scer\GAL432B extra vein tissue appears in the wing. When expression is driven by Scer\GAL4h-H10 eyes show gaps in the array of ommatidia.
Scer\GAL4Act.PU/Egfr1.A887T.UAS is an enhancer of oocyte associated follicular epithelium | somatic clone phenotype of aPKCk06403
Scer\GAL4Tub.PU/Egfr1.A887T.UAS is a non-suppressor of intestinal stem cell | somatic clone phenotype of lin-28Δ1
The reduction in total cell number per clone and reduction in number of Dl-positive intestinal stem cells per clone seen in MARCM clones in the intestine of lin-28Δ1 adults is not rescued by expression of Egfr1.A887T.Scer\UAS under the control of Scer\GAL4tub.PU.
Expression of Egfr1.A887T.Scer\UAS under the control of Scer\GAL4hs.PU partially restores cyst formation in Inx2FA42 females (branched fusomes are observed in 77% of cases), but the formation of egg chambers is not rescued in these females.
Knock-down of yki through co-expression of ykidsRNA.N.Scer\UAS in Egfr1.A887T.Scer\UAS MARCM mutant clones (under the control of Scer\GAL4esg-NP5130) does not affect intestinal stem cell proliferation.