FB2024_03 , released June 25, 2024
Allele: Dmel\RfC4A18
Open Close
General Information
Symbol
Dmel\RfC4A18
Species
D. melanogaster
Name
FlyBase ID
FBal0045034
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Amino acid replacement: Q46term.

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

    C4135848T

    Reported nucleotide change:

    C136T

    Amino acid change:

    Q46term | RfC4-PA

    Reported amino acid change:

    Q46term

    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

    Mitotic index is decreased to 0.20% in homozygous larval brains, compared to 0.94% in wild-type brains. Two types of mitotic defects are observed; more common is mitotic figures with prematurely condensed chromosomes, while less common is figures showing precocious sister chromatid separation.

    Polytene chromosomes in salivary glands in homozygous third instar larvae are underreplicated and banding is disrupted.

    Homozygous larval brains show very little incorporation of BrdU.

    The brains of mutant larvae do not halt progression through the cell cycle in response to either aphidicolin or hydroxyurea, in contrast to wild type, as they do not show a reduction in mitotic index.

    The brains of mutant larvae do not show a drop in mitotic index after treatment with either etoposide or UV irradiation, indicating a failure to arrest the cell cycle.

    Treatment with caffeine dramatically increases the mitotic index in mutant larval brain neuroblasts.

    Mutant larval brain neuroblasts arrest in mitosis in response to treatment with colchicine, as occurs in wild type.

    Homozygous larvae have no imaginal discs, suggesting a defect in imaginal disc proliferation.

    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
    Fails to complement
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (2)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (7)
    Reported As
    Symbol Synonym
    RfC40A18
    RfC4A18
    l(3)Rfc4a18
    Name Synonyms
    Secondary FlyBase IDs
      References (4)