FB2025_01 , released February 20, 2025
Allele: Dmel\Atg1JF02273
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General Information
Symbol
Dmel\Atg1JF02273
Species
D. melanogaster
Name
FlyBase ID
FBal0220663
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
Atg1 RNAi, UAS-atg1 RNAi, UAS-Atg1-RNAi, Atg1-RNAi, atg1RNAi, UAS-atg1RNAi, UAS-Atg1i, Atg1-IR
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Genomic Maps

Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UAS regulatory sequences drive expression of an inverted repeat.

Allele components
Component
Use(s)
Encoded product / tool
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Clonal expression of Atg1JF02273 under the control of Scer\GAL4Act5C.PU in the larval fat body leads to smaller cells in starved individuals, but not in well fed individuals, as compared to controls.

Flies expressing Atg1JF02273 under the control of Scer\GAL4Mef2.PU have similar lifespan, locomotion and mitochondrial structure as wild-type controls.

Expression of Atg1JF02273 under the control of Scer\GAL4phm.PO leads to massive accumulation of lipid droplets in the prothoracic gland cells of third instar larvae.

Expression of Atg1JF02273 in muscle under the control of Scer\GAL4Mef2.PU results in significant hyperglycaemia.

Expression of Atg1JF02273 under the control of Scer\GAL4Myo31DF-NP0001 results in significantly delayed midgut degradation after pupariation, with increased size of the midgut and gastric caeca 4 hrs after puparium formation, and decreased autophagy 2 hrs after puparium formation, as compared to controls.

Expression of Atg1JF02273 under the control of Scer\GAL4cg.PU results in a decrease in starvation-induced autophagy in the larval fat body, as compared to controls.

Expression of Atg1JF02273 under the control of Scer\GAL4Mef2.PR is able to completely suppress the formation of autophagosomes in the muscles of both untreated and chloroquine-treated larvae starved on low-nutrient food for 6 hours.

Glycogen breakdown occurs normally in the muscles of larvae expressing Atg1JF02273 under the control of Scer\GAL4Mef2.PR starved on low-nutrient food for 24 hours, but the rate of breakdown is reduced compared to controls.

After 3 or 6 hours of starvation, expression of Atg1JF02273 under the control of Scer\GAL4Mef2.PR significantly improves the crawling defects seen in chloroquine-treated larvae compared to controls. After 6 hours starvation, crawling is negatively affected in the absence of chloroquine treatment. In well-fed larvae there is little difference between crawling time compared to controls, either in the presence or absence of chloroquine.

Expression of Atg1JF02273 using Scer\GAL4Act5C.PP results in basal autophagy defects in larval fat body cell somatic clones.

Expression of Atg1JF02273 using Scer\GAL4Cg.PA causes a decrease in starvation-induced autophagic response in the fat body of wandering third instar larvae compared with wild-type.

Expression of Atg1JF02273 via Scer\GAL4HCH.Hand causes a decline in cardiac performance.

Expression of Atg1JF02273 via Scer\GAL4Mef2.PR causes mitochondrial abnormalities and degeneration in skeletal muscle.

External Data
Interactions
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Phenotype Manifest In
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Suppressor of
NOT Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference

Expression of Atg1JF02273 completely suppresses the eye degeneration seen when Atg1Scer\UAS.T:Hsap\MYC and Atg13Scer\UAS.T:Avic\GFP-EGFP are co-expressed under the control of Scer\GAL4GMR.PU at 18[o]C.

Co-expression of Atg1JF02273 and TorHMS00904 under the control of Scer\GAL4Myo31DF-NP0001 restores autophagy and gastric caeca contraction to levels similar to those seen in controls.

The reduction in the distance between wing veins 3 and 4 that is seen in animals expressing PrpkdsRNA.Scer\UAS.462 under the control of Scer\GAL4salm.EPv is not suppressed if they are also co-expressing Atg1JF02273.

In contrast to the expression of either transgene alone, glycogen breakdown is disrupted in the muscles of larvae co-expressing Atg1JF02273 and GlyPNIG.7254R under the control of Scer\GAL4Mef2.PR and starved on low-nutrient food for 24 hours.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
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Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (50)