FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\AP-2αHMS00653
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General Information
Symbol
Dmel\AP-2αHMS00653
Species
D. melanogaster
Name
FlyBase ID
FBal0257337
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
AP-2α RNAi, UAS-AP-2α RNAi
Key Links
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 a short 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 ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Expression of AP-2αHMS00653 under the control of Scer\GAL4ppk.PU (and Dicer-2, for efficient RNAi) results in mild but highly penetrant ddaC neuron dendrite pruning defects at 16h after puparium formation, as compared to controls.

Expression of AP-2αHMS00653 under the control of Scer\GAL4ey.PU induces a headless phenotype in pupae. Expression under the control of Scer\GAL4elav-C155 or Scer\GAL4Toll-6-D42 results in sluggish 3rd instar larvae which die. Expression under the control of Scer\GAL4elav-C155 also leads to a significant increase in the number of boutons at larval muscle 6/7 NMJs, as compared to controls; electrophysiology recording show significant increases in mEJP frequency and amplitude, significant decreases in EJP amplitude and quantal content, and a significant decline in EJP amplitude upon high-frequency stimulation at 34[o]C conditions, even after a 4min rest period.

Under starvation conditions, the expression of AP-2αHMS00653 under the control of Scer\GAL4Cg.PA results in the third instar larval fat body showing an the accumulation and enlargement of early and late endosomes (identified as GFP-FYVE and GFP-Rab7 cytoplasmic puncta, respectively), an enlargement of lysosomes (identified as LAMP-GFP puncta) and their accumulation at the cell membrane, and an accumulation and enlargement of autophagosomes (identified as GFP-Atg8 cytoplasmic puncta and p62 protein cytoplasmic puncta), as compared to starved controls. However, similar defects in early and late endosomes, lysosomes and autophagosomes are also observed under normal diet.

Expression of AP-2αHMS00653 under the control of Scer\GAL4SPARC-MI00329-GAL4 results in melanisation of the fat body.

Expression of AP-2αHMS00653 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 results in embryos with two distinct plasma membrane furrow defects. The first class of embryos exhibit various degrees of furrow loss, while the second class display abnormal plasma membrane expansions, specifically at furrow tips at both cellularisation and earlier syncytial divisions. This second class also lacks the endocytic tubules that usually emanate from the furrow canals.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
Suppressor of
NOT Suppressor of
Other
Additional Comments
Genetic Interactions
Statement
Reference

The ddaC neuron pruning defects induced by Scer\GAL4ppk.PU-driven expression of AP-2αHMS00653 are significantly enhanced by heterozygosity for prd1M56, as the persisting dendrites become significantly longer.

Maternal heterozygosity for AP-2σKG02457 enhances the furrow canal phenotype seen in embryos derived from mothers expressing AP-2αHMS00653 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16.

Maternal heterozygosity for stepk08110 enhances the furrow canal phenotype seen in embryos derived from mothers expressing AP-2αHMS00653 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16.

Maternal heterozygosity for stepSH0323 enhances the furrow loss phenotype seen in embryos derived from mothers expressing AP-2αHMS00653 under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
AP-2αHMS00653
α-AdaptinHMS00653
Name Synonyms
Secondary FlyBase IDs
    References (15)