FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Apc2d40
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General Information
Symbol
Dmel\Apc2d40
Species
D. melanogaster
Name
FlyBase ID
FBal0137665
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: C677term.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

C24166267A

Amino acid change:

C677term | Apc2-PA; C657term | Apc2-PB; C677term | Apc2-PC

Reported amino acid change:

C677term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

Repositioning of the mitotic spindle during anaphase in testis somatic cyst stem cells is normal in Apc2d40/Apc2ΔS males.

Embryos maternally mutant for Apc2d40 exhibit incomplete actin rings that are occasionally associated with apparent spindle collisions. Although actin pseudocleavage furrows initiate in some of these embryos, they do not extend normally.

18% of Apc2g10 maternally mutant syncytial embryos and 19% of embryos from Apc2d40/+ mothers show movement of over 2% of cortical nuclei into the embryo interior, compared to 0-3% of wild-type embryos.

Apc2d40/+ embryos derived from Apc2d40 homozygous mothers show no dominant-negative effects with respect to cell division.

The cuticle of an average Apc2d40 maternal/zygotic embryo shows an anterior hole, is 50-60% the length of wild-type and has 2-3 patches of denticles remaining.

Mutants exhibit an increase in size in every segment of the cII cluster of slou expressing muscle founder cells. A change in size of cI cluster is also seen in 4% of hemisegments.

Apc2ΔS/Apc2d40 males have germline stem cells with mispositioned centrosomes, misoriented spindles or detached spindles.

Homozygotes survive to adulthood. Homozygotes have a normal number of retinal neurons. Embryos derived from homozygous females mated to wild-type males have a wild-type cuticle. Homozygous embryos derived from homozygous females mated to heterozygous males show an expansion of naked cuticle. Mutant embryos derived from Apc2d40/Df(3R)w6 females mated to Df(3R)w6/+ males nearly completely lack all ventral denticles.

In Apc2d40 maternal and zygotic mutants most cells take on posterior fates and secrete naked cuticle.

Apc2d40 is not temperature sensitive, and is homozygous viable in the first generation. Homozygous mutant flies mated together produce embryos showing a more complete excess naked cuticle phenotype than that produced by the Apc2ΔS stock.

Homozygous embryos derived from homozygous female germline clones show loss of nuclei from the surface of the embryo during syncytial development. Actin caps appear generally normal, although they are reduced in size where nuclei have been lost.

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

The ventral cuticle of ApcQ8, Apc2d40 double mutant embryos is naked.

Expression of AxnScer\UAS.cHa under the control of Scer\GAL4da.G32 blocks the naked-cuticle phenotype of ApcQ8, Apc2d40 double mutant embryos.

Expression of AxnScer\UAS.T:Src64B,T:Zzzz\FLAG under the control of Scer\GAL4da.G32 has no effect on the naked-cuticle phenotype of ApcQ8, Apc2d40 double mutant embryos.

Expression of Apc2Scer\UAS.T:Avic\GFP under the control of Scer\GAL4da.G32 restores wild-type patterning of the ventral cuticle in ApcQ8, Apc2d40 double mutant embryos.

Expression of Apc2Scer\UAS.T:Src64B,T:Zzzz\FLAG under the control of Scer\GAL4da.G32 fails to restore wild-type patterning of the ventral cuticle in ApcQ8, Apc2d40 double mutant embryos.

Triple mutants for AxnS044230, ApcQ8 and Apc2d40 have naked ventral embryonic epidermis.

The ventral denticle belt phenotype of AxnS044230, ApcQ8, Apc2d40 triple mutants is suppressed by expression of AxnScer\UAS.cHa under the control of Scer\GAL4da.G32.

Expression of AxnScer\UAS.T:Src64B,T:Zzzz\FLAG under the control of Scer\GAL4da.G32 has no effect on the ventral denticle belt phenotype of AxnS044230, ApcQ8, Apc2d40 triple mutants.

Expression of Apc2Scer\UAS.T:Avic\GFP under the control of Scer\GAL4da.G32 has no effect on the ventral denticle belt phenotype of AxnS044230, ApcQ8, Apc2d40 triple mutants.

Expression of Apc2Scer\UAS.T:Src64B,T:Zzzz\FLAG under the control of Scer\GAL4da.G32 has no effect on the ventral denticle belt phenotype of AxnS044230, ApcQ8, Apc2d40 triple mutants.

ApcQ8 Apc2d40 double mutant homozygotes derived from heterozygous parents differentiate a normal larval cuticle but die during the larval stage. ApcQ8 Apc2d40 double mutant clones in the wing autonomously form marginal structures, adopting the fate of those marginal cells that are closest to the clone; they form bristles in the anterior and thin tapered hairs in the posterior. The clones can occupy up to 1/3 of the wing surface. ApcQ8 Apc2d40 double mutant clones result in outgrowths in the proximal leg and duplications in the distal leg. The duplications arise from the dorsal side of the leg and contain both homozygous clone cells and neighbouring heterozygous cells. Double mutant clones are rarely found in parts of the leg that have differentiated into dorsal structures. Double mutant clones are frequently found in ventral structures and ventral bristles in these clones are often morphologically normal. ApcQ8 Apc2d40 double mutant clones in the eye show transformation into ectopic head cuticle. These clones can occupy up to half the eye. ApcQ8 Apc2d40 double mutant clones also produce mutant phenotypes in the head cuticle, antennae, labial disc derivatives, notum, tergites and genitalia. The expansion of naked cuticle seen in embryos derived from Apc2d40 females mated to Apc2d40 males is enhanced if the maternal or zygotic dose of Apc is reduced by half (using ApcQ8); in these double mutant embryos most denticles are eliminated. Embryos derived from ApcQ8 Apc2d40 double mutant germline clones (lacking maternal but not zygotic Apc and Apc2) have some cuticle defects but often hatch and survive to adulthood. Animals derived from ApcQ8 Apc2d40 double mutant germline clones and also lacking zygotic Apc (animal is homozygous for ApcQ8) die either during embryonic or larval stages and differentiate partially naked cuticles. The cuticle defects of embryos derived from ApcQ8 Apc2d40 double mutant germline clones are also enhanced if the embryos lack zygotic Apc2 (embryo is homozygous for Apc2d40). Expression of ApcScer\UAS.cHa under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 rescues Apc2d40 embryos (that lack both maternal and zygotic Apc2) to adulthood.

Apc2d40, ApcQ8 double homozygotes die a first instar larvae.

Apc2d40 ApcQ8 double zygotic mutants are embryonic viable and exhibit a wild-type cuticle pattern, but die as larvae. Apc2d40 ApcQ8 maternal and zygotic double mutants exhibit a much stronger embryonic cuticle phenotype than Apc2d40 maternal and zygotic single mutants. Maternal and zygotic double mutant cuticles are shorter, and, unlike Apc2d40 maternal and zygotic single mutants, most embryos completely lack denticles. Maternal and zygotic double mutants also exhibit a complete failure of head involution. Dorsally, all cells are transformed to the fate normally adopted by posterior cells, and thus all secrete fine dorsal hairs. These embryos also exhibit slight abnormalities in dorsal closure not seen in the single mutant. Embryos receiving paternal wild-type copies of Apc2 and Apc are rescued to viability. Patches of ectopic wing margin bristles are seen in the wing blades of animals in which Apc2d40 ApcQ8 double mutant clones have been induced. Ectopic bristles are also seen in the nota of these animals.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

Apc2d40 is more severe than Apc2ΔS, though is probably not a null allele.

Apc2 alleles can be divided into three categories based on their embryonic cuticle phenotypes, from weak to moderate to strong: Apc2e90 = Apc2b5 = Apc2N175K < Apc2c9 = Apc2ΔS = Apc2d40 < Apc2g41 = Apc2f90 = Apc2g10.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
References (20)