FB2026_02 , released June 18, 2026
Allele: Dmel\pugD
Open Close
General Information
Symbol
Dmel\pugD
Species
D. melanogaster
Name
FlyBase ID
FBal0060593
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Caused by aberration
    Cytology
    Description

    The pug coding region is fused to approximately 1kb of highly repetitive DNA. Transcription and translation of both parts are required for the mutant phenotype. The repetitive DNA consists of ~140 nearly perfect repeats of AGAGAGA, a significant component of centric heterochromatin.

    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

    Eye pigment phenotype whereby pigment is more intense at the eye periphery. Variegation occurs such that more pigmented patches occur internal to the eye, revealed dramatically in a mutant background for v, where pugD is revealed to almost completely remove pteridines in the middle of the eye. The periphery of the eye remains pigmented. A small portion of the mutant flies have concave dents in the eye as if it were structurally weak. Homozygotes sometimes have rough eyes.

    Affects pteridine (red) and ommochrome (brown) pigments. Pteridine is eliminated in the middle of the eye so that eyes are pigmented only at the edge. Causes a variegated reduction in ommochrome pigmentation.

    Eliminates pteridines in the middle of the eye. Also causes variegated reduction in ommochrome level.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    Additional Comments
    Genetic Interactions
    Statement
    Reference
    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments

    The repetitive DNA of the fusion allele may be responsible for the variegated aspect of the mutant phenotype - by association of the pug locus with centric heterochromatin.

    External Crossreferences and Linkouts ( 6 )
    Crossreferences
    GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
    GenBank Protein - A collection of sequences from several sources, including translations from annotated coding regions in GenBank, RefSeq and TPA, as well as records from SwissProt, PIR, PRF, and PDB.
    UniProt/TrEMBL - Automatically annotated and unreviewed records of protein sequence and functional information
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    PugD
    pugD
    Name Synonyms
    Secondary FlyBase IDs
      References (8)