FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
Allele: Dmel\Mms19EY00797
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General Information
Symbol
Dmel\Mms19EY00797
Species
D. melanogaster
Name
FlyBase ID
FBal0217091
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
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Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    Cytology
    Description
    Allele components
    Component
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    Mutations Mapped to the Genome
    Curation Data
    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
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    Modifiers Based on Experimental Evidence ( 0 )
    Disease
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    Disease-implicated variant(s)
     
    Phenotypic Data
    Phenotypic Class
    Phenotype Manifest In
    Detailed Description
    Statement
    Reference

    Mms19EY00797 mutant larvae develop slowly but reach third instar stage, however the third instar larvae have noticeably smaller brains than wild-type, completely lack recognizable imaginal discs and fail to pupate.

    24.5% of embryos from mothers carrying Mms19EY00797 mutant germline clones (created using the OvoD technique) hatch into larvae if fertilized by Mms19+/+ fathers and 10.5% if fertilized by Mms19EY00797/+ fathers. Majority of the embryos display various cell cycle defects: spindle defects, kinked axis of division, many missing nuclei, elongated spindle in metaphase, chromosome segregation defects, and centrosomal defects in division cycle 10-13.

    Embryos from Mms19EY00797 mutant mothers also carrying Mms19EGFP (to rescue the maternal effect cell cycle defects) and expressing Zzzz\vhhGFP4deGradFP.hb.bcd3'UTR to knock-down the rescue Mms19EY00797 transgene during embryogenesis only, leads to various and abundant cell cycle defects: Improper chromosome segregation and chromosomal bridges in anaphase and telophase, significantly elongated spindle in metaphase, spindle crossovers, multipolar spindles, kinked axis of division and loss of nuclei in one or more large areas.

    External Data
    Interactions
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    Phenotypic Class
    Suppressed by
    Phenotype Manifest In
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    The various maternal effect cell cycle defects observed in early embryos from from mothers carrying Mms19EY00797 mutant germline clones (created using the OvoD technique) are partially suppressed by combination with a single copy of Xpdunspecified loss-of-function or a deficiency covering the Xpd locus (apart from the chromosome segregation defects, the frequency of which is actually increased).

    The complete loss of imaginal discs characteristic for Mms19EY00797 mutant third instar larvae can be rescued by simultaneous expression of Cdk7UAS.cNa, Mat1UAS.cNa and CycHUAS.cNa under the control of Scer\GAL4da.G32 in the mutant background, but the overall structure of the discs is visibly abnormal.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    Combination with one or two copies of Mms19EGFP rescues the lethality of Mms19EY00797/Df(3R)ED5147 mutants. Expression of Mms19EGFP in Mms19EY00797 germline mutant females (created using the OvoD technique) at least partially rescues all of the various cell cycle defects (spindle defects, kinked axis of division, many missing nuclei, elongated spindle in metaphase, chromosome segregation defects, and centrosomal defects) observed in their progeny at embryonic division cycle 10-13.

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    Mutant
    Wild-type
    Stocks (2)
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    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    Mms19EY00797
    Name Synonyms
    Secondary FlyBase IDs
      References (2)