C13226234T
R217C | Dp-PA; R213C | Dp-PB; R189C | Dp-PC
follicle cell & nucleus
heterochromatin & nurse cell (with Df(2R)vg56)
nuclear membrane & nurse cell (with Df(2R)vg56)
nurse cell (with Df(2R)vg56)
ommatidium (with Dpa2)
ovary (with Df(2R)vg56)
Dpa1/Df(2R)vg56 follicle cells show increased ploidy compared to control cells by FACS analysis.
The ovaries of Dpa1/Df(2R)vg56 females are smaller than wild-type but have the normal complement of nurse and follicle cells. Occasionally, degenerating early egg chambers (stage 8 and earlier) are seen. The predominant defects in Dpa1/Df(2R)vg56 females are a failure of nurse cells to deposit their contents into the oocyte and degenerate and an increased amount of heterochromatic DNA in the nurse cell nuclei. In homozygous Dpa1 egg chambers, unlike wild-type (where nurse cells undergo apoptosis during stages 12 to 13 and have degenerated by stage 14), degeneration of nurse cells is abnormal and occurs late if at all. Dpa1/Df(2R)vg56 mutant mothers lay few eggs. In the rare cases in which mature eggs are laid most are unfertilized, apparently due to defects in chorion structure. The few fertilized embryos arrest in early division cycles. In addition, the morphology of the polar bodies are affected. In embryos from these females meiosis is completed, but polar body chromosomes are either condensed, improperly arranged or dispersed in the embryo.
Eggs laid by hemizygous females have thin eggshells. Hemizygous ovaries show abnormal patterns of BrdU incorporation during stage 10B and later stages. The follicle cell nuclei fail to initiate amplification in most egg chambers, while in some stage 10B egg chambers genomic replication rather than amplification is seen.
Disrupt G[[1]]-S transcription late in embryogenesis, DNA replication still occurs.
Hemizygotes exhibit rough eyes, incomplete wing vein, thin and short bristles and etched tergites. Females lay eggs with thin chorions. More females than males in progeny.
Dpa1/Dpa2 flies exhibit reduced eyes, missing and disorganised ommatidia, stunted, missing and disorganised bristles. Daily heat shocks of Dphs.PD rescued proliferation defects to normal looking eyes.
Heat induced expression of E2f1hs.PD at 25[o]C provides significant rescue of the mutant phenotype, but higher levels of expression dampen the rescue.
Dpa1 is an enhancer of visible phenotype of Mmus\Shisa5UAS.cGa, Scer\GAL4ey.PH
Dpa1 is an enhancer of abnormal size phenotype of Mmus\Shisa5UAS.cGa, Scer\GAL4ey.PH
Dpa1/Dpa2 is a suppressor of abnormal mitotic cell cycle phenotype of RhebUAS.cSa, Scer\GAL4Act5C.PP
Dpa1/Dpa2 is a suppressor of abnormal mitotic cell cycle phenotype of MycUAS.cZa, Scer\GAL4Act5C.PP
Dpa1/Dpa2, Scer\GAL4Act5C.PP, dapUAS.cdNa has abnormal mitotic cell cycle phenotype
Dpa1/Dpa2, Scer\GAL4Act5C.PP, Wee1UAS.cPa has abnormal mitotic cell cycle phenotype
Dpa1/Dpa2, Scer\GAL4Act5C.PP, Wee1UAS.cPa has cell lethal | partially phenotype
Dpa1 is an enhancer of eye phenotype of Mmus\Shisa5UAS.cGa, Scer\GAL4ey.PH
Dpa1/Dpa2 is a suppressor of mitotic cell cycle phenotype of RhebUAS.cSa, Scer\GAL4Act5C.PP
Dpa1/Dpa2 is a suppressor of mitotic cell cycle phenotype of MycUAS.cZa, Scer\GAL4Act5C.PP
Dpa1/Dpa2, Scer\GAL4Act5C.PP, dapUAS.cdNa has mitotic cell cycle phenotype
Dpa1/Dpa2, Scer\GAL4Act5C.PP, Wee1UAS.cPa has mitotic cell cycle phenotype
Cells expressing dapScer\UAS.cdNa driven by Scer\GAL4Act5C.PP in a Dpa1/Dpa2 background, divide more slowly than controls. Cells expressing weeScer\UAS.cPa driven by Scer\GAL4Act5C.PP in a Dpa1/Dpa2 background, divide more slowly than controls. These cells are also subviable. Cells expressing dmScer\UAS.cZa or RhebScer\UAS.cSa driven by Scer\GAL4Act5C.PP in a Dpa1/Dpa2 background, the compensatory elongation of the G2 phase, is not as pronounced seen in dmScer\UAS.cZa expressing cells.
Dpa1 enhances the eye phenotypes seen when Mmus\Shisa5Scer\UAS.cGa is expressed under the control of Scer\GAL4dpp.PH.
Daily heat shocks of Dphs.PD in Dpa1/Dpa2 individuals rescues the proliferation defects to normal looking eyes.
Heat induced expression of Dphs.PD at 25oC partially rescues the lethality, males are fertile. Recovered adults still exhibit the visible eye, wing vein and bristle defects and are still female sterile. Induced expression at 37oC completely rescues the lethality and all developmental phenotypes are suppressed. Daily heat shocks of Dphs.PD rescued proliferation defects seen in Dpa1/Dpa2 flies leading to normal looking eyes.