Expression of Hsap\HTT16Q.FL.Scer\UAS under the control of Scer\GAL4elav.PU has no significant effect on nighttime sleep. A small, but significant increase in daytime sleep bout number is seen, but overall daytime rest and average daytime sleep bout length are normal.
Expression of Hsap\HD16Q.FL.Scer\UAS using the strong Scer\GAL4GMR.PF driver does not result in depigmentation or disorganization of ommatidia.
Flies expressing Hsap\HD16Q.FL.Scer\UAS using Scer\GAL4C164 do not show impaired motor performance as a function of age, as measured by a flying assay.
Aged flies expressing Hsap\HD16Q.FL.Scer\UAS using Scer\GAL4C164 do not show a neurodegenerative phenotype: motor neurons innervating the indirect flight muscles and neuromuscular junctions are normal.
Excitatory junction potentials (EJPs) at neuromuscular junctions of third instar larvae expressing Hsap\HD16Q.FL.Scer\UAS using Scer\GAL4elav-C155 are similar to controls at 1.2 mM, 0.25 mM and 0.6 mM extracellular Ca[2+].
Resting synaptic Ca[2+] levels at presynaptic terminals are elevated by ~2-fold in Hsap\HD16Q.FL.Scer\UAS, Scer\GAL4elav-C155 larvae.
Hsap\HTT16Q.FL.UAS/Scer\GAL4arm.PS is a suppressor | partially of short lived phenotype of Hsap\MAPTUAS.GFP, Scer\GAL4shot-OK307, htt98E2
Hsap\HTT16Q.FL.UAS/Scer\GAL4arm.PS is a suppressor | partially of abnormal locomotor behavior | progressive phenotype of Hsap\MAPTUAS.GFP, Scer\GAL4shot-OK307, htt98E2
Hsap\HTT16Q.FL.UAS, Scer\GAL4shot-OK307 is a suppressor | partially of adult thorax phenotype of Hsap\MAPTUAS.GFP, Scer\GAL4shot-OK307, htt98E2
Hsap\HTT16Q.FL.UAS, Scer\GAL4shot-OK307 is a suppressor | partially of adult somatic muscle cell of thorax phenotype of Hsap\MAPTUAS.GFP, Scer\GAL4shot-OK307, htt98E2
Expression of Hsap\MAPTScer\UAS.T:Avic\GFP under the control of Scer\GAL4shot-OK307 in the htt98E2 homozygous mutant background induces prominent collapse of the thorax due to severe loss of the muscles below, these phenotypes are not observed in either the Hsap\MAPTScer\UAS.T:Avic\GFP expressing flies or the htt98E2 mutants alone and can be rescued by co-expression of Hsap\HTT16Q.FL.Scer\UAS.
The age-dependent loss of climbing ability as well as the reduced lifespan characteristic for htt98E2 homozygous adults is partially suppressed by expression of Hsap\HTT16Q.FL.Scer\UAS under the Scer\GAL4arm.PS driver and further worsened by expression of Hsap\MAPTScer\UAS.T:Avic\GFP under the control of Scer\GAL4shot-OK307 in the mutant background. This worsened phenotype can in turn also be fully partially rescued by co-expression of Hsap\HTT16Q.FL.Scer\UAS.