UASt regulatory sequences drive expression of an inverted repeat.
chromosome | larval stage, with Scer\GAL4Act.PU
Flies expressing Shmt2GD8851 under the control of Scer\GAL4da.PU display severely reduced eclosion rate compared to controls, the adults that manage to eclose show much decreased lifespan and significant climbing ability defects. Scer\GAL4elav.PU-driven expression leads to fragmented mitochondrial network in larval neural tissue with decreased mean mitochondrial length.
Adults expressing CG3011GD8851 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.
Expression under the control of Scer\GAL4pnr-MD237 results in bristle morphology defects on the notum in 10-20% or 40-50% of the Scer\GAL4pnr-MD237 expression domain, depending on the insertion line used.
Expression under the control of Scer\GAL4pnr-MD237 results in the absence of 0% or 20-30% of the Scer\GAL4pnr-MD237-expressing area of the notum, depending on the insertion line used.
Scer\GAL4da.PU/ShmtGD8851 is an enhancer of visible | adult stage phenotype of Pink1B9
Scer\GAL4da.PU/ShmtGD8851 is an enhancer of partially lethal phenotype of park25
Scer\GAL4da.PU/ShmtGD8851 is a non-enhancer of partially lethal phenotype of Pink1B9
Scer\GAL4da.PU/ShmtGD8851 is an enhancer of adult thorax phenotype of Pink1B9
The lethality and dented thorax phenotype of Pink1B9 mutants is enhanced upon Scer\GAL4da.PU-driven expression of Shmt2GD8851. A strong increase in lethality of park25 mutants is also seen upon expression of either Shmt2GD8851 (hardly any adults can be recovered).