In 10-day and 20-day old flies expressing Hsap\SNCAS129D.Scer\UAS under the control of Scer\GAL4elav.PU, the number of dopaminergic neurons in the dorsomedial clusters is significantly reduced compared to controls.
Scer\GAL4GMR.PU-mediated expression of Hsap\SNCAS129D.Scer\UAS causes prominent retinal degeneration.
1 day old flies expressing Hsap\SNCAS129D.Scer\UAS under the control of Scer\GAL4elav.PU have a normal number of dorsomedial dopaminergic neurons, while 10 day old flies show a substantial loss of these neurons compared to wild type. No significant loss of neurons in the cortex or attenuation of neuropil is seen.
Adults expressing Hsap\SNCAS129D.Scer\UAS under the control of Scer\GAL4GMR.PF have prominent retinal degeneration with substantial loss of photoreceptors and support cells. Marked cell loss is seen by 10 days.
Hsap\SNCAS129D.UAS, Scer\GAL4elav.PU has abnormal neuroanatomy | adult stage phenotype, suppressible by SharkUAS.cFa, Scer\GAL4elav.PU
Hsap\SNCAS129D.UAS, Scer\GAL4elav.PU has dopaminergic neuron | adult stage phenotype, suppressible by SharkUAS.cFa, Scer\GAL4elav.PU
Hsap\SNCAS129D.UAS, Scer\GAL4GMR.PU has ommatidium | adult stage phenotype, suppressible by SharkUAS.cFa, Scer\GAL4GMR.PU
Coexpression of sharkScer\UAS.cFa significantly rescues the neurotoxicity of Scer\GAL4elav.PU-mediated Hsap\SNCAS129D.Scer\UAS expression.
Coexpression of sharkScer\UAS.cFa attenuates the retinal degeneration caused by Scer\GAL4GMR.PU-mediated Hsap\SNCAS129D.Scer\UAS expression.