The expression of Kap-α3UASp.cMa under the control of Scer\GAL4GMR.PF does not result to any obvious eye phenotypes compared to controls.
Kap-α3UASp.cMa, Scer\GAL4GMR.PF is an enhancer of abnormal eye color phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Kap-α3UASp.cMa, Scer\GAL4GMR.PF is an enhancer of visible phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Kap-α3UASp.cMa, Scer\GAL4GMR.PF is an enhancer of increased cell death | adult stage phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Kap-α3UASp.cMa, Scer\GAL4elav.Switch.PO is a non-enhancer of short lived phenotype of Hsap\ATXN370Q.UAS, Scer\GAL4elav.Switch.PO
Kap-α3UASp.cMa, Scer\GAL4elav.Switch.PO is a non-enhancer of abnormal locomotor behavior | adult stage phenotype of Hsap\ATXN370Q.UAS, Scer\GAL4elav.Switch.PO
Kap-α3UASp.cMa, Scer\GAL4GMR.PF is an enhancer of eye phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Kap-α3UASp.cMa, Scer\GAL4ninaE.PT is a non-enhancer of eye | progressive phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4ninaE.PT
Kap-α3UASp.cMa, Scer\GAL4ninaE.PT is a non-enhancer of ommatidium | progressive phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4ninaE.PT
Expression of Kap-α3Scer\UAS.P\T.cMa under the control of Scer\GAL4nos.UTR.T:Hsim\VP16 does not rescue the sterility of PenD14 females.
The rough eye phenotype and associated depigmentation and necrosis induced by the expression of Hsap\ATXN3tr.Q78.UAS.Tag:HA under the control of Scer\GAL4GMR.PF are severely exacerbated by the co-expression of Kap-α3UASp.cMa, leading to prominent degeneration of the ommatidia. The late onset eye defects (i.e. disorganized ommatidia and tissue dissociation associated with the appearance of vacuoles) induced by the Scer\GAL4ninaE.PT-driven expression do not seem to be affected by the co-expression of Kap-α3UASp.cMa.
The decreased lifespan and the decreased adult locomotion induced by the adulthood-only expression of Hsap\ATXN370Q.UAS under the control of Scer\GAL4elav.Switch.PO and RU-486 treatment are not significantly affected by the co-expression of Kap-α3UASp.cMa.