A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\foxoΔ94

General Information
SymbolDmel\foxoΔ94SpeciesD. melanogaster
NameFlyBase IDFBal0269838
Feature typealleleAssociated geneDmel\foxo
Allele class
MutagenP-element activity
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Description
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FB2013_03
FB2013_02
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hide Nature of the Allele
Allele class
Mutagen
Mutations Mapped to the Genome
Type
Location
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Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
UniProtKB/TrEMBL
Progenitor genotype
Nature of the lesion
Statement
Reference
Imprecise excision of P{GT1}foxo[BG01018] generate a deletion that spans over 20kb of the foxo locus, removing part of the predicted promoter region as well as several coding exons.
Cytology
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Statement
Reference
foxo[Δ94] mutant neuromuscular junctions display enhanced microtubule stability compared to controls.
foxo[Δ94] homozygotes and foxo[Δ94]/foxo[25] transheterozygotes are delayed in egg-adult development time and are smaller in size compared to controls, with a significant reduction in both body weight and wing area. Homozygous foxo[Δ94] females are shorter lived than controls and lay fewer eggs. foxo[Δ94] mutant clones appear normal in size, suggesting that foxo does not act cell-autonomously to restrict cell proliferation or growth. foxo[Δ94] females display an increase in lifespan under dietary restriction.
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Reference
foxoΔ94 has viable | RU486 conditional phenotype, non-suppressible by InRK1409A.Scer\UAS/Scer\GAL4da.Switch.PT
foxoΔ94 has viable | RU486 conditional phenotype, non-suppressible by Pi3K92ED954A.Scer\UAS.T:Hsap\MYC/Scer\GAL4da.Switch.PT
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Reference
foxoΔ94 is a suppressor | partially of long lived | drug conditional phenotype of Scer\GAL4Ilp3.PB, rprScer\UAS.C
foxoΔ94 is a suppressor of long lived | RU486 conditional phenotype of InRK1409A.Scer\UAS, Scer\GAL4da.Switch.PT
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Statement
Reference
foxoΔ94 is a non-suppressor of viable | RU486 conditional phenotype of Pi3K92ED954A.Scer\UAS.T:Hsap\MYC, Scer\GAL4da.Switch.PT
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Statement
Reference
Expression of foxo[Scer\UAS.P\T.cSa] within the median neurosecretary cells (MNCs) under the control of Scer\GAL4[da.G32] rescues the lethality seen in chico[1];foxo[Δ94] mutants. Expression of InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32] in foxo[Δ94] mutant flies results in an age-related increase in survival compared to controls, but this is less than in wild-type flies expressing InR[K1409A.Scer\UAS]. A foxo[Δ94] mutant background suppresses the extension in lifespan seen upon RU486-induced expression of InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.Switch.PT]. Expression of InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32] does not affect the viability of foxo[Δ94] flies. Late ablation of the mNSCs through expression of rpr[Scer\UAS.C] under the control of Scer\GAL4[Ilp3.PB] does not affect the viability of foxo[Δ94] flies. Adult onset ubiquitous expression of InR[K1409A.Scer\UAS] or Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of the RU486-inducible Scer\GAL4[da.Switch.PT] has no effect on the viability of foxo[Δ94] flies. foxo[Δ94] mutant females expressing InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32] show reduced egg laying compared with controls. foxo[Δ94] mutant females expressing InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.Switch.PT] treated with RU486 lay significantly fewer eggs than their uninduced controls. foxo[Δ94] mutant flies expressing InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32] all survive for longer on food supplemented with 20mM paraquat compared to controls (but shorter compared to expression in a wild-type background). A foxo[Δ94] background suppresses the DTT resistance seen in flies expressing InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32]. A foxo[Δ94] background fully suppresses the tissue-restricted growth inhibition seen in the eye upon expression of InR[K1409A.Scer\UAS] under the control of Scer\GAL4[ey.PH]. Removal of foxo through a foxo[Δ94] background does not suppress the developmental delay or reduced body size seen in flies expressing InR[K1409A.Scer\UAS] under the control of Scer\GAL4[da.G32]. A foxo[Δ94] mutant background suppresses the extension in lifespan seen upon RU486-induced expression of Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[da.Switch.PT]. Adult onset ubiquitous expression of Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of the RU486-inducible Scer\GAL4[da.Switch.PT] has no effect on the viability of foxo[Δ94] flies. A foxo[Δ94] mutant background does not affect the decrease in egg-laying found upon adult-specific ubiquitous expression of Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[da.Switch.PT]. foxo[Δ94] mutant flies expressing Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[da.Switch.PT] all survive for longer on food supplemented with 20mM paraquat compared to controls (but shorter compared to expression in a wild-type background). A foxo[Δ94] background suppresses the DTT resistance seen in flies expressing Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[da.Switch.PT]. foxo[Δ94] mutant flies expressing Pi3K92E[D954A.Scer\UAS.T:Hsap\MYC] under the control of Scer\GAL4[da.G32] all survive for longer on food supplemented with 20mM paraquat compared to controls (but shorter compared to expression in a wild-type background). A foxo[Δ94] background suppresses the lifespan of female flies expressing rpr[Scer\UAS.C] under the control of Scer\GAL4[Ilp3.PB], almost to wild-type levels. foxo[Δ94] mutant females expressing rpr[Scer\UAS.C] under the control of Scer\GAL4[da.G32] show reduced egg laying compared with controls. In a foxo[Δ94] mutant background, Scer\GAL4[Ilp3.PB] driven expression of rpr[Scer\UAS.C] leads to significantly fewer eggs being laid than in controls.
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Bloomington
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Research paper
Nechipurenko and Broihier, 2012, J. Cell Biol. 196(3): 345--362
FoxO limits microtubule stability and is itself negatively regulated by microtubule disruption. [FBrf0217391]
Rynes et al., 2012, Mol. Cell. Biol. 32(19): 3949--3962
Activating transcription factor 3 regulates immune and metabolic homeostasis. [FBrf0219385]
Slack et al., 2011, Aging Cell 10(5): 735--748
dFOXO-independent effects of reduced insulin-like signaling in Drosophila. [FBrf0215229]