Expressing Rab1S25N.UAS.YFP from the middle third instar larval stage onwards under the combined control of Scer\GAL4GSG2295 and RU486 feeding leads to ddaC neurons showing strong pruning defects in pupae (16h APF) despite of normal dendrite arbors in the white prepupal stage.
Expression of Rab1S25N.UAS.YFP under the control of CtxGlia-SplitGal4 (Hsim\VP16AD.nrv2 and Scer\GAL4DBD.wrapper.932i) leads to an altered cortex glial morphology in third instar larvae when compared to controls.
When Rab1S25N.Scer\UAS.T:Avic\GFP-YFP is expressed using Scer\GAL4ppk.PG, transgenic animals show defective nociception response.
Expression of Rab1S25N.Scer\UAS.T:Avic\GFP-YFP under the control of Scer\GAL4Ilp2.PW results in a dramatic (>40%) reduction in adult fly weight. Pupal size is also dramatically reduced and flies eclose, on average, ~2 days later than control flies. Hemolymph levels of trehalose and glucose are elevated compared to controls. Fewer Insulin Producing Cells (IPCs) are seen in the larvae and IPC neuronal morphology is dramatically disrupted. Dendritic arborisations are missing while the axonal bundles are mostly intact. Limiting Rab1S25N.Scer\UAS.T:Avic\GFP-YFP expression to late larval development onwards using Scer\GAL80ts.αTub84B avoids the IPC developmental defects.
The kinetics of maturation of phagosomes containing pHrodo-conjugated S. aureus by adult hemocytes expressing Rab1S25N.Scer\UAS.T:Avic\GFP-YFP under the control of Scer\GAL4Hml.Δ are not significantly different from those seen in control hemocytes.
Rab1S25N.UAS.YFP, Scer\GAL4ppk.PG is a non-enhancer of abnormal heat stress response phenotype of Scer\GAL4ppk.PG, Spt-IC129W.UAS