FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Mkp3GS801
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General Information
Symbol
Dmel\Mkp3GS801
Species
D. melanogaster
Name
FlyBase ID
FBal0194675
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
    Associated Insertion(s)
    Cytology
    Description
    Allele components
    Component
    Use(s)
    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

    Embryos that express Mkp3GS801 under the control of Scer\GAL4btl.PS show normal tracheal development up to stage 13. At stage 14, several primary dorsal branches and ganglionic branches fail to form or contain only one or two cells. Additionally, breaks can be observed using luminal markers in thin unicellular branches, such as the most ventral (lateral trunk posterior) and dorsal branches. Branch breaks increase with time and in late stages of embryogenesis sometimes almost no branches appear continuous. In vivo imaging shows that tracheal cells appear more rounded than in wild-type embryos and that breaks occur due to tracheal cells pulling apart; at first the cells remain connected by long cytoplasmic extensions that can eventually break.

    The tracheal tree of Scer\GAL4btl.PS>Mkp3GS801 embryos shows few apoptotic cells, indicating that cell death is not the major reason for the branch integrity phenotype.

    The tracheal tubes of stage 16 Scer\GAL4btl.PS>Mkp3GS801 embryos show a thinner accumulation of cortical actin compared to controls.

    The embryonic tracheal phenotype is also observed when Mkp3GS801 is expressed under the control of Scer\GAL4arm.PS, Scer\GAL4ptc-559.1 or Scer\GAL469B.

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

    The branch integrity defects of Scer\GAL4btl.PS>Mkp3GS801 embryos are increased when these embryos have a rl10a/+ background relative to a wild-type background.

    Coexpression of rlSem.cUa.UAS suppresses the tracheal branching defects of Scer\GAL4btl.PS>Mkp3GS801 embryos.

    Expression of Mkp3GS801 under the control of Scer\GAL4btl.PS in a btlLG19/+ background does not affect the penetrance of the Scer\GAL4btl.PS>Mkp3GS801 branch integrity phenotype but results in a significant increase in failure of branch formation.

    Xenogenetic Interactions
    Statement
    Reference

    Coexpression of Mkp3GS801 with BacA\p35Scer\UAS.cHa, under the control of Scer\GAL4btl.PS does not suppress the branch integrity and primary branching defects of Mkp3GS801 embryos.

    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    Mkp3GS801
    Name Synonyms
    Secondary FlyBase IDs
      References (1)