FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Ssedft
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General Information
Symbol
Dmel\Ssedft
Species
D. melanogaster
Name
FlyBase ID
FBal0318601
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description

    3bp deletion, which results in the loss of residues Phe265 and Gly266 and their replacement by a Cys residue.

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

    3 bp deletion (TTG) at position 794 from the initiation codon. Phe265 and Gly266 are replaced with a Cys. The resulting protein which is shorter by a single amino acid is not functional.

    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

    Ssedft/Ssedft, Ssedft/Sse13m or Ssedft/Df(3L)ZN47 larval brains have telomeric fusions and endoreduplication phenotypes: neuroblasts have few dividing cells (around 3 metaphases per brain) and most cells are endoreduplicated (showing bundles of 2, 4, and 8 sister chromosomes and ploidy levels from 4n to 32n), and a large number of metaphases contain 64 (16n) or more than 64 chromosomes; some endoreduplicated chromosomes are also fused at their ends, giving rise to multicentric chromosome configurations and rings. Telomeric fusion frequency is increased (ratio between number of double telomere attachments and total number of chromosomes, which in mutants does not change significantly with the degree of endoreduplication).

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Suppressed by
    Phenotype Manifest In
    Suppressed by
    Statement
    Reference
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Su(var)205g.T:Disc\RFP partially suppresses the telomeric fusion phenotype (but not endoreduplication) seen in Ssedft/Ssedft larval brain neuroblasts.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    Expression of SseScer\UAS.T:Ivir\HA1 driven by Scer\GAL469B rescues telomeric fusions and endoreduplication phenotypes in Ssedft/Ssedft larval brain neuroblasts.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer

    The "l(3)05146" chromosome carries two separate mutations: His2Av05146 and the second site mutation Ssedft.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Name Synonyms
    diplofusedtelomeres
    Secondary FlyBase IDs
      References (2)