FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\auxI670K
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General Information
Symbol
Dmel\auxI670K
Species
D. melanogaster
Name
FlyBase ID
FBal0215598
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
dAuxI670K
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: I670K.

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

T4225185A

Amino acid change:

I670K | aux-PA; I670K | aux-PB; I670K | aux-PC; I662K | aux-PD

Reported amino acid change:

I670K

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

auxI670K/auxL78H adults exhibit rough eyes, with extra photoreceptor cells and occasional extra bristles on the notum, sternopleurum, and scutellum.

auxI670K/auxL78H mutant males, when mated to wild-type females, do not produce any embryos that hatch. Spermatids do develop in the testis, however the seminal vesicles are empty in adult male flies. The morphology of the testis hub cells appear normal in these animals. The number of germ cells is comparable to wild-type testes. Spermatid individualisation is disrupted in mutants, and migration of the investment cone along spermatid cysts does not occur normally.

auxI670K/auxG257E adults exhibit rough eyes, with extra photoreceptor cells and occasional extra bristles on the notum, sternopleurum, and scutellum.

auxI670K/auxG257E mutant males, when mated to wild-type females, do not produce any embryos that hatch. Spermatids do develop in the testis, however the seminal vesicles are empty in adult male flies. The morphology of the testis hub cells appear normal in these animals. A slightly reduced number of germ cells is observed compared to wild-type testes. Cytokinesis is mostly normal in these animals. In 5% of spermatids examined, an enlarged mitochondrial derivative associated with two nuclei is observed. Spermatid individualisation is disrupted in mutants, and migration of the investment cone along spermatid cysts does not occur normally.

Homozygous auxI670K flies can survive until adulthood.

Mutants homozygous for auxI670K exhibit several morphological defects, including rough eyes, extra bristles, missing wing veins, and male and female sterility. The eyes of auxI670K mutants are grossly disorganised, with patches of brown necrotic tissues on the surface. This rough eye phenotype shows temperature dependence, as the eye roughness is significantly milder for mutants raised at 18oC than those grown at 25oC. At a higher temperature, such as 29</up>o</up>C, the homozygous mutant state is completely lethal.

auxI670K mutants exhibit supernumerary vibrissae, and frequently, extra anterior sternopleural bristles. Occasionally, extra bristles are also detected on the notum or scutellum of mutant animals. At low frequency, some mutant animals exhibit wings with incompletely formed posterior crossveins, and absent wing vein material at the posterior wing vein margin. The penetrance and severity of these phenotypes are more pronounced in mutant animals heteroallelic for auxW328X/auxI670K and auxW1150X/auxI670K raised at 18oC.

Sections of auxI670K mutant retina exhibit disrupted ommatidia. Supernumerary photoreceptor cells are detected in 39.67% of auxI670K mutant clusters. These extra photoreceptors are either outer (cells with large rhabdomeres; 21.42%) or inner (cells with small rhabdomeres; 18.25%), suggesting that auxI670K is not affecting the determination of a particular photoreceptor cell fate.

elav-positive cell clusters are clearly disorganised in auxI670K tissues, with supernumerary elav-positive cells in some of the clusters.

Embryos derived from the mating of auxI670K homozygous females with wild-type males exhibit highly organised central and peripheral nervous systems with characteristic numbers of neuro-positive cells. In contrast, embryos maternally deficient but zygotically heterozygous for auxI670K exhibit mild hypertrophy in the ventral nerve cord, disorganisation and slight reduction in the peripheral nervous system, and abnormal body morphology.

Homozygous mutant auxI670K eye discs exhibit excessive elav-positive cells.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhanced by
Enhancer of
Statement
Reference

auxI670K/aux[+] is an enhancer of posterior wing margin phenotype of N264-39

auxI670K/aux[+] is an enhancer of eye phenotype of NUAS.cMa, Scer\GAL4GMR.PF

NOT Enhancer of
Statement
Reference

auxI670K/aux[+] is a non-enhancer of eye phenotype of EgfrUAS.cBa, Scer\GAL4GMR.PF

Additional Comments
Genetic Interactions
Statement
Reference

Expression of Hsc70-4K71S.Scer\UAS under the control of Scer\GAL4GMR.PF in a auxI670K/+ background generates a severe rough eye phenotype, more severe than expression of Hsc70-4K71S.Scer\UAS under the control of Scer\GAL4GMR.PF in a wild-type background.

The expression of ClcScer\UAS.T:Avic\GFP-EGFP under the control of Scer\GAL4Act5C.PI greatly reduces the viability of auxI670K mutants. In rare escapers, the eyes are rougher, and there is dramatic enhancement of the wing phenotypes, including severe notching, wing vein thickening, and ectopic vein formation.

Homozygous mutant auxI670K eye discs that also express NICN.Scer\UAS (under the control of Scer\GAL4GMR.PF) exhibit a reduction in the number of elav-positive cells, indicating that N is epistatic to aux.

A heterozygous auxI670K background increases the severity of both the penetrance and the phenotype of N264-39 heterozygous mutants.

Although animals heterozygous for auxI670K are normal, this background strongly reduces the eye size and enhances the rough eye of NScer\UAS.cMa;Scer\GAL4GMR.PF animals.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of auxFL.βTub85D.T:Disc\RFP-mRFP in auxI670K/auxG257E mutants rescues male sterility. The rough eye and supernumerary bristle phenotypes are not rescued.

Expression of auxΔK.βTub85D.T:Disc\RFP-mRFP in auxI670K/auxG257E mutants rescues male sterility.

Expression of auxCJ.βTub85D.T:Disc\RFP-mRFP in auxI670K/auxG257E mutants rescues male sterility.

Expression of auxΔJ.βTub85D.T:Disc\RFP-mRFP in auxI670K/auxG257E mutants fails to rescue male sterility.

Expression of auxΔC.βTub85D.T:Disc\RFP-mRFP in auxI670K/auxG257E mutants fails to rescue male sterility.

Expression of auxScer\UAS.cHa (under the control of Scer\GAL4Act5C.PI) completely rescues the rough eye phenotype of auxI670K.

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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)