FB2024_03 , released June 25, 2024
Allele: Dmel\BEAF-32NP6377
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General Information
Symbol
Dmel\BEAF-32NP6377
Species
D. melanogaster
Name
FlyBase ID
FBal0223596
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
BEAFNP6377
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    Cytology
    Description

    Insertion in a protein coding exon common to both BEAF-32 A and B isoforms.

    Allele components
    Component
    Use(s)
    Inserted element
    Mutations Mapped to the Genome
    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

    BEAF-32NP6377/Df(2R)BSC429 animals and homozygous BEAF-32NP6377 retinal clones (covering the entire retina) have an increased proportion of pale R8 photoreceptors and a reciprocally decreased proportion of yellow R8 photoreceptors, compared to controls.

    FlyBase curator comment: FBrf0219796 reports that the chromosome carrying the P{GawB}BEAF-32NP6377 insertion is homozygous lethal and causes neoplastic growth phenotypes. A subsequent report (FBrf0224638) provides evidence that these phenotypes are not due to an effect on BEAF-32, but are instead due to second-site mutations on the chromosome carrying the P{GawB}BEAF-32NP6377 insertion.

    External Data
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    Phenotypic Class
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    Additional Comments
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    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (1)
    Notes on Origin
    Discoverer

    The homozygous larval lethality of the NP6377 chromosome is not due to the P{GawB}BEAF-32NP6377 insertion in BEAF-32, but is instead due to second site mutation(s): the lethality of the NP6377 chromosome is not rescued by BEAF-32+t5 or BEAF-32EGFP, and BEAF-32AB-KO (a null allele of BEAF-32) complements the lethality of the NP6377 chromosome.

    Flies carrying BEAF-32AB-KO over the NP6377 chromosome were found to be viable and could be maintained as a healthy stock over 25 generations. This was unexpected as BEAF-32AB-KO/BEAF-32AB-KO homozygous females are almost sterile (see FBrf0200670). This suggests that in addition to the second site lethality, the NP6377 chromosome also carries another second site mutation: a dominant mutation that suppresses the female fertility defect caused by a lack of BEAF-32 protein. FlyBase curator comment: this second site dominant suppressor of BEAF-32 mutant female sterility has subsequently been named Tofu1 (see FBrf0255826).

    The two second site mutations on the NP6377 chromosome (lethality and dominant suppressor of BEAF-32 mutant female sterility) are separable and therefore do not appear to be caused by the same mutation.

    Separable from: Tofu1.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (2)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (5)