The presence of RU486 from day 2 of adulthood extends the median lifespan of female flies expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 on average by 6%.
The presence of RU486 from day 2 of adulthood extends the median lifespan of foxoΔ94 female flies expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 on average by 10%.
Expressing foxoScer\UAS.cFa specifically in the mNSCs in the adult brain, using the Scer\GAL4Ilp2.215-55 driver, extends the lifespan of female flies in both wild-type and foxoΔ94 mutants.
Induction of foxoScer\UAS.cFa expression in the gut and fat body, under the control of Scer\GAL4Switch1.106 enhances the climbing ability of female flies throughout their lifespan, observed as an increase in the proportion of high, or combined medium and high, climbers. This enhancement is seen in both wild-type and foxoΔ94 backgrounds.
Induction of foxoScer\UAS.cFa expression in adulthood, under the control of Scer\GAL4Switch1.106 (and RU486) has no effect on fecundity in either wild-type or foxoΔ94 mutants, but has an effect on body weight and protein content.
Expression of foxoScer\UAS.cFa in the adult gut and fat body under the control of Scer\GAL4Switch1.106 (in the presence of RU486) results in an extended lifespan compared to controls.
Expression of foxoScer\UAS.cFa specifically in the adult gut and under the control of Scer\GAL4TIGS-2 (in the presence of RU486) has no major effect on lifespan compared to controls. Stored triacylglycerol (TAG) levels are also reduced compared to controls. Gut integrity and feeding appear normal.
Ectopic expression of foxoScer\UAS.cFa in the developing wing, under the control of Scer\GAL4ptc-559.1 induces apoptosis and the subsequent loss of the wing anterior cross vein.
Motor neuronal overexpression of foxoScer\UAS.cFa under the control of Scer\GAL4Rapgap1-OK6 does not result in neuromuscular junction overgrowth. These larvae display a modest reduction in the number of microtubule loops compared with wild-type.
Female re-mating behaviour is not altered in flies expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 24 hours after mating to wild-type flies.
Expression of foxoScer\UAS.cFa under the control of Scer\GAL4Lsp2.PH rescues the increase in triglyceride levels and the heart defects normally caused by a high-fat diet.
Expression of foxoScer\UAS.cFa under the simultaneous control of both Scer\GAL4Scer\UAS.cHa and Scer\GAL4tin.cBa does not rescue the increase in triglyceride levels caused by a high-fat diet. However, the heart defects normally caused by a high-fat diet are rescued in these animals.
Overexpression of foxoScer\UAS.cFa in muscles under the control of Scer\GAL4Mhc.PW does not affect developmental growth and differentiation (as estimated by body weight and sarcomere assembly). Overexpression of foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW results in delayed accumulation of age-related protein aggregates in muscles.
Overexpression of foxoScer\UAS.cFa in adult muscles under the control of Scer\GAL4Mef2.PR and Scer\GAL80ts.αTub84B significantly preserves muscle protein homeostasis, while the muscles of wild-type animals display increased accumulation of protein aggregates. Compared to syngenic controls, the age-related accumulation of protein aggregates in retinas, brains and the peripheral fat body of the abdomen is also decreased in flies overexpressing foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW.
Muscle functionality gradually decreases in wild-type aging flies, resulting in impaired climbing and flight ability. Overexpression of foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW significantly preserves muscle strength during aging.
Overexpression of foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW in muscles is sufficient to significantly extend longevity compared with wild type by increasing the median and maximum life span of flies.
Food intake of flies is decreased in response to overexpression of foxoScer\UAS.cFa in muscles via Scer\GAL4Mhc.PW.
The body weight of adult flies overexpressing foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW does not significantly differ from that of syngenic controls.
There is a significant decrease in the hemolymph glucose concentration compared with syngenic control in flies overexpressing foxoScer\UAS.cFa under the control of Scer\GAL4Mhc.PW
Expression of foxoScer\UAS.cFa under the control of Scer\GAL4Ccap.PP results in the loss of adult-specific neurite projections; many central neurites and efferents are lost.
Females expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 (in the presence of RU486) show an increase in mean and maximum lifespan compared with controls.
Females expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 (in the presence of RU486) show an increase in median life-span and reduced fecundity compared to controls. These females also show increased resistance to paraquat. No effect on life-span is seen in males expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 (in the presence of RU486).
When foxoScer\UAS.cFa is driven by Scer\GAL4bun-Switch1.32 (in adults fed on mifepristone) the median lifespan can increased by as much as 56%.
In contrast to wild-type flies, the stress-induced heart failure rate of foxoScer\UAS.cFa, when under the control of both Scer\GAL4tin.cBa and Scer\GAL4Scer\UAS.cHa, does not increase with age.
When expression is driven by Scer\GAL4GMR.PF the eye is reduced and the ommatidial pattern disrupted.
Scer\GAL4GMR.PF, foxoUAS.cFa has visible phenotype, enhanceable by Pi3K92ED954A.UAS.Tag:MYC, Scer\GAL4GMR.PF
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, non-enhanceable by Su(var)205HMS00278/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by morHMS01267/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by osaHMS01738/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by IswiHMS00628, Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has abnormal adult locomotory behavior phenotype, suppressible by IswiHMS00628, Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by Etl1HMS00829, Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has chemical resistant phenotype, suppressible by morHMS01267/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has chemical resistant phenotype, suppressible by IswiHMS00628, Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by domHMS00142/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, suppressible by Tip60HM05049/Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa has abnormal adult locomotory behavior phenotype, suppressible by morHMS01267/Scer\GAL4Switch1.106
Scer\GAL4Act.PU, foxoUAS.cFa has decreased cell size | somatic clone | larval stage phenotype, suppressible by Scer\GAL4Act.PU/Xbp1UAS.s.Tag:V5
Scer\GAL4Act.PU, foxoUAS.cFa has decreased size | somatic clone | larval stage phenotype, suppressible by Scer\GAL4Act.PU/Xbp1UAS.s.Tag:V5
Scer\GAL4Cg.PA, foxoUAS.cFa has decreased body size | larval stage phenotype, suppressible | partially by Xbp1UAS.s.Tag:V5/Scer\GAL4Cg.PA
Scer\GAL4Cg.PA, foxoUAS.cFa has abnormal developmental rate phenotype, suppressible | partially by Xbp1UAS.s.Tag:V5/Scer\GAL4Cg.PA
Scer\GAL4Switch1.106, foxoUAS.cFa, pntP1.UAS has short lived phenotype, suppressible by aopACT.UAS/Scer\GAL4Switch1.106
Scer\GAL4TIGS-2, foxoUAS.cFa, pntP1.UAS has short lived phenotype, suppressible | partially by Scer\GAL4TIGS-2/aopACT.UAS
Scer\GAL4Switch1.106, foxoUAS.cFa has long lived | female phenotype, non-suppressible by Su(var)205HMS00278/Scer\GAL4Switch1.106
foxoUAS.cFa/Scer\GAL4GMR58E02 is an enhancer of short lived | recessive phenotype of Fer2MB09480
foxoUAS.cFa/Scer\GAL4Switch1.106 is an enhancer of short lived phenotype of Scer\GAL4Switch1.106, pntP1.UAS
Scer\GAL4TIGS-2/foxoUAS.cFa is an enhancer of short lived phenotype of Scer\GAL4TIGS-2, pntP1.UAS
foxoUAS.cFa, Scer\GAL4Switch1.106 is a non-enhancer of short lived phenotype of Mi-2HMS00301, Scer\GAL4Switch1.106
foxoUAS.cFa/Scer\GAL4Switch1.106 is a suppressor of short lived phenotype of Scer\GAL4Switch1.106, domHMS00142
foxoUAS.cFa/Scer\GAL4Switch1.106 is a suppressor of short lived phenotype of Scer\GAL4Switch1.106, Tip60HM05049
foxoUAS.cFa/Scer\GAL4GMR58E02 is a suppressor | partially of decreased cell number | recessive | adult stage | progressive phenotype of Fer2MB09480
foxoUAS.cFa/Scer\GAL4GMR58E02 is a suppressor | partially of abnormal locomotor behavior | recessive phenotype of Fer2MB09480
Scer\GAL4how-24B/foxoUAS.cFa is a suppressor of abnormal locomotor behavior | recessive | adult stage phenotype of park25
Scer\GAL4ple.PF/foxoUAS.cFa is a suppressor of abnormal neuroanatomy | adult stage phenotype of park25
Scer\GAL4how-24B/foxoUAS.cFa is a suppressor of abnormal flight | recessive phenotype of park25
foxoUAS.cFa, Scer\GAL4Switch1.106 is a non-suppressor of short lived phenotype of Mi-2HMS00301, Scer\GAL4Switch1.106
Scer\GAL4Switch1.106, foxoUAS.cFa, nejHMS01507 has short lived phenotype
Scer\GAL4Switch1.106, aopHMS01256, foxoUAS.cFa has short lived phenotype
Pink1B9, Scer\GAL4unspecified, foxoUAS.cFa has lethal phenotype
Scer\GAL4GMR.PF, foxoUAS.cFa has eye phenotype, enhanceable by Pi3K92ED954A.UAS.Tag:MYC, Scer\GAL4GMR.PF
Scer\GAL4GMR.PF, foxoUAS.cFa has ommatidium phenotype, enhanceable by Pi3K92ED954A.UAS.Tag:MYC, Scer\GAL4GMR.PF
Scer\GAL4Act.PU, foxoUAS.cFa has larval fat cell | somatic clone phenotype, suppressible by Scer\GAL4Act.PU/Xbp1UAS.s.Tag:V5
Scer\GAL4Act.PU, foxoUAS.cFa has lipid droplet | somatic clone | larval stage phenotype, suppressible by Scer\GAL4Act.PU/Xbp1UAS.s.Tag:V5
foxoUAS.cFa/Scer\GAL4GMR58E02 is a suppressor | partially of adult dopaminergic PAM neuron | adult stage | progressive phenotype of Fer2MB09480
Scer\GAL4how-24B/foxoUAS.cFa is a suppressor of indirect flight muscle cell phenotype of park25
Scer\GAL4how-24B/foxoUAS.cFa is a suppressor of mitochondrion phenotype of park25
Scer\GAL4ple.PF/foxoUAS.cFa is a suppressor of dopaminergic PPL1 neuron phenotype of park25
The expression of foxoUAS.cFa under the control of Scer\GAL4GMR58E02 partially suppresses the progressive decrease in the number of adult PAM neurons and the decreased adult locomotion capacity observed in Fer2MB09480 homozygotes, while further reducing their decreased lifespan.
Co-expression of foxoScer\UAS.cFa and aopHMS01256 in the adult midgut and fat body under the control of Scer\GAL4Switch1.106 (in the presence of RU486) results in a reduced lifespan compared to controls.
Expression of foxoScer\UAS.cFa enhances the reduction in lifespan seen when pntP1.Scer\UAS is expressed in the adult midgut and fat body under the control of Scer\GAL4Switch1.106 (in the presence of RU486). This phenotype is completely suppressed upon expression of aopACT.Scer\UAS. Co-expression of foxoScer\UAS.cFa and pntP1.Scer\UAS also enhances the reduction in stored triacylglycerol (TAG) levels seen when either transgene is expressed alone. Gut integrity and feeding appear normal.
Expression of foxoScer\UAS.cFa enhances the reduction in lifespan seen when pntP1.Scer\UAS is expressed in the adult midgut under the control of Scer\GAL4TIGS-2 (in the presence of RU486). This phenotype is partially suppressed upon expression of aopACT.Scer\UAS.
Flies co-expressing pntP1.Scer\UAS and foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 are starvation sensitive after 5 days in the presence of RU486, and this phenotype can be reversed upon expression of aopACT.Scer\UAS.
Expression of foxoScer\UAS.cFa driven by Scer\GAL4how-24B significantly partially suppresses flight and climbing defects as well as muscle degeneration and mitochondrial disruption in park25/park25 flies; foxoScer\UAS.cFa driven by Scer\GAL4ple.PF significantly suppresses loss of dopaminergic PPL1 neurons in 30 day old park25/park25 flies. Expression of foxoScer\UAS.cFa in a Pink1B9/Pink1B9 background results in lethality.
foxoUAS.cFa/Scer\GAL4GMR58E02 partially rescues foxoΔ94
foxoUAS.cFa/Scer\GAL4Switch1.106 partially rescues foxoΔ94
Scer\GAL4Ilp2.215-55/foxoUAS.cFa partially rescues foxoΔ94
foxoUAS.cFa/Scer\GAL4P2.4.Pdf fails to rescue foxo25/foxo21
The expression of foxoUAS.cFa under the control of Scer\GAL4GMR58E02 rescues the decreased number of dopaminergic PAM neurons in the adult brain but enhances the decreased lifespan presented by foxoΔ94 homozygotes.
The presence of RU486 from day 2 of adulthood extends the median lifespan of foxoΔ94 female flies expressing foxoScer\UAS.cFa under the control of Scer\GAL4Switch1.106 on average by 10%.
Expressing foxoScer\UAS.cFa specifically in the mNSCs in the adult brain, using the Scer\GAL4Ilp2.215-55 driver, extends the lifespan of female flies in foxoΔ94 mutants.
Induction of foxoScer\UAS.cFa expression in the gut and fat body, under the control of Scer\GAL4Switch1.106 enhances the climbing ability of female flies throughout their lifespan, observed as an increase in the proportion of high, or combined medium and high, climbers. This enhancement is seen in a foxoΔ94 background.
Induction of foxoScer\UAS.cFa expression in adulthood, under the control of Scer\GAL4Switch1.106 (and RU486) has no effect on fecundity in foxoΔ94 mutants, but has an effect on body weight and protein content.
Expression of foxoScer\UAS.cFa under the control of Scer\GAL4Lk6-DJ634 rescues the circadian arrhythmia seen in foxo21/foxo25 mutants. Phototaxis is not affected by paraquat treatment in these mutants.