Expression of Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 in larval body wall sensory neurons under the control of Scer\GAL4RluA1 has no apparent effect on larval da neuron viability.
Expression of Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 in larval body wall sensory neurons under the control of Scer\GAL4RluA1 does not result in the formation of cytoplasmic aggregates.
Expression of Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 in larval body wall sensory neurons under the control of Scer\GAL4RluA1 does not affect dendrite elaboration in da neurons of the dorsal cluster. Dendrites fully cover the field and project towards the dorsal midline to meet the contralateral dendrites, and also fully extend to segment boundaries.
The speed of locomotion is not different in Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 expressing larva (driven by Scer\GAL4RluA1) compared to wild-type controls. The trajectory of larval locomotion is also not affected.
Segmental nerve bursting activity is normal in larvae expressing Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 under the control of Scer\GAL4RluA1.
Flies co-expressing Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP and Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 in the developing eye through the Scer\GAL4GMR.PF driver exhibit a normal eye phenotype.
Overexpression of RhebScer\UAS.cPa in the developing eye of Hsap\HTT18Q.Ex1.Scer\UAS.T:Avic\GFP-EGFP.T:Zzzz\nls1 mutants (both transgene under the control of Scer\GAL4GMR.PF results in a rough eye phenotype with bristle disorganization.