UASt regulatory sequences drive expression of Hsap\TARDBP tagged with an N-terminal Tag:HA from a construct that allows site-specific integration into the genome.
17-AAG treatment suppresses neurodegeneration in rough eye model of neurodegenerative disease.
Expression of Hsap\TARDBPScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF leads to moderate rough eye phenotype.
Adulthood-only expression of Hsap\TARDBPScer\UAS.T:Ivir\HA1 under the combined control of Scer\GAL4Toll-6-D42, Scer\GAL80ts.αTub84B leads to decreased locomotor activity and a decrease in lifespan compared to controls.
Hsap\TARDBPUAS.Tag:HA, Scer\GAL4GMR.PF has visible | adult stage phenotype, non-enhanceable by Hsp67BcUAS.Tag:V5, Scer\GAL4GMR.PF
Hsap\TARDBPUAS.Tag:HA, Scer\GAL4Toll-6-D42, Scer\GAL80ts.αTub84B has short lived phenotype, suppressible | partially by CG14207EP1348, Scer\GAL4Toll-6-D42, Scer\GAL80ts.αTub84B
Hsap\TARDBPUAS.Tag:HA, Scer\GAL4Toll-6-D42, Scer\GAL80ts.αTub84B has abnormal locomotor behavior phenotype, suppressible | partially by CG14207EP1348, Scer\GAL4Toll-6-D42, Scer\GAL80ts.αTub84B
Hsap\TARDBPUAS.Tag:HA, Scer\GAL4GMR.PF has eye phenotype, non-enhanceable by Hsp67BcUAS.Tag:V5, Scer\GAL4GMR.PF
Hsap\TARDBPUAS.Tag:HA, Scer\GAL4GMR.long has ommatidium phenotype, suppressible | partially by CG14207EP1348, Scer\GAL4GMR.long
The moderate rough eye phenotype characteristic for adult flies expressing Hsap\TARDBPScer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF is not significantly modified by co-expression of Hsp67BcScer\UAS.T:SV5\V5.
Overexpression of CG14207EP1348 under the control of Scer\GAL4GMR.long partially suppresses the ommatidium phenotype caused by Hsap\TARDBPScer\UAS.T:Ivir\HA1 expression.
Overexpression of CG14207EP1348 at the permissive temperature under the control of both Scer\GAL4D42 and Scer\GAL80ts.αTub84B partially suppresses the shortened lifespan phenotype caused by Hsap\TARDBPScer\UAS.T:Ivir\HA1 expression alone.
Overexpression of CG14207EP1348 at the permissive temperature under the control of both Scer\GAL4D42 and Scer\GAL80ts.αTub84B partially suppresses the locomotor defects caused by Hsap\TARDBPScer\UAS.T:Ivir\HA1 expression alone.