UASt regulatory sequences drive expression of an inverted repeat.
Adulthood-only expression of Pi3K59FKK107602 under the combined control of Scer\GAL4tub.PU and Gal80[ts] leads to intestinal barrier disfunction (as shown by the abnormal permeability to a non-absorbable food dye) and leads to the failure to induce autophagy (assessed by the lysosome and autophagosome marker, Lysotracker) in the adult fat body in response to starvation, as compared to controls. Adulthood-only expression of Pi3K59FKK107602 under the combined control of Scer\GAL4Myo31DF-NP0001 and Gal80[ts] leads to a significantly increased in the posterior midgut cell size, as compared to controls.
The expression of Pi3K59FKK107602 under the control of Scer\GAL4GMR.PU leads to a significant decrease in the number of ommatidia and disrupts the ommatidial array, as compared to controls. Expression under the control of Scer\GAL4Ddc.PL leads to a significant decrease in longevity and to a progressive decrease in adult locomotor ability in climbing assays, as compared to controls.
Co-expression of Pi3K59FKK107602 does not rescue the detachment of the dorsal temporary internal oblique muscles which is seen in pharate adults expressing mtmdsRNA.cVa.Scer\UAS under the control of Scer\GAL4Mef2.PR.
Pi3K59FKK107602, Scer\GAL4GMR.PU has visible | adult stage phenotype, enhanceable by BuffyUAS.cQa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4GMR.PU has visible | adult stage phenotype, enhanceable by Hsap\SNCAUAS.cFa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4Ddc.PL has short lived phenotype, suppressible by BuffyUAS.cQa, Scer\GAL4Ddc.PL
Pi3K59FKK107602, Scer\GAL4Ddc.PL has abnormal locomotor behavior | adult stage | progressive phenotype, suppressible by BuffyUAS.cQa, Scer\GAL4Ddc.PL
Pi3K59FKK107602, Scer\GAL4GMR.PU is an enhancer of visible | adult stage phenotype of Hsap\SNCAUAS.cFa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4Ddc.PL is an enhancer of short lived phenotype of Hsap\SNCAUAS.cFa, Scer\GAL4Ddc.PL
Pi3K59FKK107602, Scer\GAL4Ddc.PL is a non-enhancer of abnormal locomotor behavior | adult stage | progressive phenotype of Hsap\SNCAUAS.cFa, Scer\GAL4Ddc.PL
Pi3K59FKK107602, Scer\GAL4GMR.PU has eye phenotype, enhanceable by BuffyUAS.cQa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4GMR.PU has ommatidium phenotype, enhanceable by BuffyUAS.cQa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4GMR.PU has eye phenotype, enhanceable by Hsap\SNCAUAS.cFa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4GMR.PU has ommatidium phenotype, enhanceable by Hsap\SNCAUAS.cFa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4GMR.PU is an enhancer of eye phenotype of Hsap\SNCAUAS.cFa, Scer\GAL4GMR.PU
Pi3K59FKK107602, Scer\GAL4Mef2.PR is a non-suppressor of muscle cell of abdominal temporary eclosion muscle DA phenotype of Scer\GAL4Mef2.PR, mtmRNAi.cVa.UAS
Both the decreased longevity and the progressive decrease in adult locomotion induced by the expression of Pi3K59FKK107602 under the control of Scer\GAL4Ddc.PL are suppressed by the co-expression of BuffyScer\UAS.cQa. The decreased number of ommatidia and the disrupted ommatidial array induced by the expression of Pi3K59FKK107602 under the control of Scer\GAL4GMR.PU are also suppressed by the co-expression of BuffyScer\UAS.cQa.
The co-expression of Pi3K59FKK107602 and Hsap\SNCAScer\UAS.cFa under the control of Scer\GAL4GMR.PU leads to a decrease in the number of ommatidia and consequent disruption of the ommatidial array, both of which are more severe than upon each single expression condition.
The co-expression of Pi3K59FKK107602 enhances the decreased longevity, but not the progressive decrease in adult locomotion, induced by the expression of Hsap\SNCAScer\UAS.cFa under the control of Scer\GAL4Ddc.PL.