62kb deletion extending proximally from P{EP}tauEP3203, removing almost all the tau locus, including the exons that encode the microtubule binding domain.
Phenotypes in the Hsap\APP1-40.Scer\UAS.T:SS-nec Alzheimer's Disease model are suppressed when tauMR22 is transheterozygous with tauEP3203.
tauMR22/+ larvae do not exhibit specific accumulation of a subset of synaptic cargo in axons, as compared to controls.
The oocyte nucleus is mislocalised to the central or lateral region of the oocyte in 58% of stage 10 egg chambers of females containing homozygous tauMR22 germline clones.
Germline and follicle cell clones of Df(3R)MR22 have no microtubule defects.
tauMR22/tau[+] is a suppressor of abnormal neuroanatomy | pupal stage phenotype of Scer\GAL4ppk.PG, par-1HMS00405
tauMR22/tau[+] is a suppressor | partially of abnormal neuroanatomy | somatic clone | pupal stage phenotype of par-1Δ-16
tauMR22/tauEP3203 is a suppressor of abnormal locomotor behavior | adult stage | progressive | RU486 conditional phenotype of Hsap\APPArctic.UAS.Tag:SS(nec), Scer\GAL4elav.Switch.PO
tauMR22 is an enhancer of terminal tracheal cell | embryonic stage phenotype of shot3
tauMR22 is an enhancer of tracheal lumen | embryonic stage phenotype of shot3
tauMR22/tau[+] is a suppressor of larval multidendritic class IV neuron | pupal stage phenotype of Scer\GAL4ppk.PG, par-1HMS00405
tauMR22/tau[+] is a suppressor of dendrite | pupal stage phenotype of Scer\GAL4ppk.PG, par-1HMS00405
tauMR22/tau[+] is a suppressor | partially of larval multidendritic class IV neuron | somatic clone | pupal stage phenotype of par-1Δ-16
tauMR22/tau[+] is a non-suppressor of axon | larval stage phenotype of Scer\GAL4BG380, par-1UAS.cSa
tauMR22/+ fails to suppress the axonal transport defects seen in flies expressing par-1Scer\UAS.cSa under the control of Scer\GAL4BG380.
The pruning defects observed in class IV dendritic arborizing neurons of pupae expressing par-1HMS00405 under the control of Scer\GAL4ppk.PG or in par-1Δ-16 mutant MARCM clones are significantly suppressed by combination with a single copy of tauMR22.
tauMR22/tauEP3203 suppresses the climbing defects seen in flies expressing Hsap\APPArctic.Scer\UAS.T:SS-nec under the control of Scer\GAL4elav.Switch.PO from 2 day post-eclosion onwards (expression induced by feeding flies RU486). This rescue is further enhanced by feeding the flies lithium in adulthood.
tauMR22 is rescued by tauUASp.mGFP6/Scer\GAL4VP16.mat.αTub67C