Expression of tauScer\UAS.P\T.T:Avic\GFP-m6 under the control of Scer\GAL4BG380 in larval neuromuscular junctions does not lead to specific accumulation of a subset of synaptic cargo in axons, as compared to controls.
Expression of tauScer\UAS.P\T.T:Avic\GFP-m6 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 has no effect on oocyte nucleus localisation.
tauUASp.mGFP6/Scer\GAL4VP16.mat.αTub67C is a suppressor | partially of oocyte nucleus phenotype of Scer\GAL4VP16.mat.αTub67C, par-1UAS.ΔSP.GFP
Scer\GAL4elav-C155/tauUASp.mGFP6 is a suppressor | partially of neuropil phenotype of futscholk1
The penetrance of the oocyte mislocalisation phenotype seen in egg chambers of females expressing par-1Scer\UAS.ΔSP.T:Avic\GFP under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 is reduced by co-expression of tauScer\UAS.P\T.T:Avic\GFP-m6 (from 96% to 33%).
Flies that express tauScer\UAS.P\T.T:Avic\GFP-m6 under the control of Scer\GAL4elav-C155 show a 25% reduction in the size of vacuoles that develop in the mechanosensory neuropil compared to futscholk1 flies that do not express the transgene.
Expression of tauScer\UAS.P\T.T:Avic\GFP-m6 significantly rescues the retinal degeneration seen in one week old flies expressing tauGD8682 under the control of Scer\GAL4GMR.PU.
Expression of tauScer\UAS.P\T.T:Avic\GFP-m6 partially rescues the semi-lethality seen when tauGD8682 is expressed under the control of Scer\GAL4Appl.G1a.
The oocyte nucleus mislocalisation defect seen in tauMR22 germline clones is rescued by expression of tauScer\UAS.P\T.T:Avic\GFP-m6 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16.