Imprecise excision of P{PZ}pnt05484 has deleted sequence from the P1 isoform specific exon '1'.
Oenocytes are completely absent in pnt05484Δ33 homozygous or pnt05484Δ33/pntMI03880 transheterozygous stage 15 embryos lack oenocytes, unlike controls.
Adult midgut intestinal stem cell somatic MARCM clones homozygous for pnt05484Δ33 do not display any growth defects during regeneration: The rate of mitosis upon infection with Pseudomonas entomophila in the mosaic midgut is comparable to controls.
pnt05484Δ33 mutant type II neuroblast (NB) clones appear much smaller than wild type clones, with the number of both immature and mature intermediate neural progenitors reduced by almost 50%. Accordingly, the number of GMCs is also reduced by half. Cell cycle progression appears normal in pnt05484Δ33 mutant type II NBs.
pnt05484Δ33 homozygous clones in the dorsal air sac primordium grow and normally but never contribute to the tip of the primordium.
In somatic clones mutant for pnt05484Δ33 in third instar eye discs, most R2-5 photoreceptors do not undergo G1 arrest (about 17% do), and even fewer (about 4%) differentiate.
Homozygous and pnt05484Δ33/pntΔ88 embryos have wild-type midgut development.
Eggs laid by mosaic females (generated using Scer\FRT/Scer\FLP1 recombination system) that have a clone of mutant follicle cells in the dorsal-anterior region or a clone that covers the entire follicle cell layer exhibit a single broad dorsal appendage 4 times wider than a wild type appendage. This is not a fusion of the two appendages but cells from the middle region taking on an appendage-producing cell fate.
Clones in the eye are missing photoreceptors.
pnt05484Δ33 is a non-enhancer of visible phenotype of BacA\p35GMR.PH, DpGMR.PD, E2f1GMR.PD
The growth of intestinal stem cell somatic MARCM clones expressing cicKK100838 under the control of Scer\GAL4tub.PU in the adult midgut is not reduced by combination with pnt05484Δ33.
Does not enhance the phenotype of E2fGMR.PD DpGMR.PD BacA\p35GMR.PH flies.