FB2024_03 , released June 25, 2024
Allele: Dmel\Msp3003prime
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General Information
Symbol
Dmel\Msp3003prime
Species
D. melanogaster
Name
FlyBase ID
FBal0218044
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
MSP-300Δ3'
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Caused by aberration
    Cytology
    Description

    Df(2L)Msp-300-3 removes the 3' section of the Msp-300 locus, including the KASH domain, between PBac{WH}f05524 and P{XP}d01768.

    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 ( 1 )
    Disease
    Evidence
    References
    Modifiers Based on Experimental Evidence ( 1 )
    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

    Body wall muscles in Msp3003prime homozygous third instar larvae frequently show nuclei clustering together or in contact with each other, instead of the typically even spaced in controls.

    The striated muscle in Msp-3003prime mutant third instar larvae exhibits aggregation of the myonuclei and aberrant nuclear shape, as well as variable nuclear size. In contrast to wild to wild type, where the nuclei are tightly associated with the myofibril compartment, Msp-3003prime mutant myonuclei are dissociated from the core acto-myosin compartment and float above it. The sarcomeric organisation of the muscles is retained.

    Muscles from third instar larvae homozygous mutant for Msp-3003prime show clustering of the mitochondria and endoplasmic reticulum.

    Homozygous klarΔ1-18 mutant larvae exhibit a 70% reduction in their motility compared to wild type.

    Adult flies homozygous mutant for Msp-3003prime are unable to fly.

    Msp-3003prime homozygotes are semi-lethal (approximately 20% of expected homozygotes survive). They do not display any obvious phenotype and move normally. Over time, the movements become slower and the larvae die before entering the second instar. There is no detectable difference in the arrangement or the movement of the body wall muscles of wild-type and mutant individuals when observing the larvae in polarised light.

    Msp-3003prime homozygous flies, in which the KASH domain coding part of the Msp-300 locus is deleted, exhibit normal eyes.

    Msp-3003prime homozygous females lay normal eggs.

    Msp-3003prime germline clones lay normal eggs, with no observable defects in nuclear position or nuclear architecture in the egg chambers.

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

    Female Msp-3003prime;klarmarb-BX12 double mutants lay normal eggs and exhibit wild-type egg chambers.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    A Dp(2;1)B19 background rescues the semi-lethality of Msp-3003prime mutants.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (9)
    Reported As
    Symbol Synonym
    Df(2L)Msp-300-3
    Msp-3003prime
    Msp3003prime
    Msp300Δ3'
    msp-300d3
    Name Synonyms
    Secondary FlyBase IDs
      References (5)