FB2024_03 , released June 25, 2024
Allele: Dmel\Larbypass
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General Information
Symbol
Dmel\Larbypass
Species
D. melanogaster
Name
FlyBase ID
FBal0086815
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
Dlarbypass, Dlarbyp
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description

    4bp deletion between the two PTPase domains of Lar, leading to truncation of the gene product shortly before the beginning of PTP-D2.

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

    Position of mutation on reference sequence inferred by FlyBase curator based on author statement (Figure 4). 4bp deletion between the two PTPase domains of Lar, leading to truncation of the gene product shortly before the beginning of PTP-D2.

    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

    43% of pupal R1-R6 axons mutant for Larbypass do not extend their axons, or show aberrant axon extension, targeting, and morphology.

    Stage 14 oocytes from Lar2127/Larbypass females are indistinguishable from wild-type.

    Around 10% of Larbypass mutants show an ISNb bypass phenotype.

    Around 10% Larbypass mutants display a motor axon guidance phenotype known as "ISNb bypass" in which ISNb axons successfully split away from the ISN pathway at the exit junction, but can fail to grow into the muscle field at their normal entry point. Instead, such axons travel along parallel to the ISN, underneath the muscles, until they reach the dorsal edge of the VLM field.

    Homozygous and heterozygous larvae have fewer boutons (both type Ib and type Is) at the muscle 6/7 neuromuscular junction than wild type.

    ISNb axons often show a "bypass" phenotype (failing to enter the normal muscle target domain just outside the ventral nerve cord and instead following the intersegmental nerve towards dorsal targets) in homozygous embryos. ISNb axons also show a bypass phenotype in Larbypass/Lar5.5 or Larbypass/Lar13.2 embryos. ISNb axons also show a bypass phenotype in Larbypass/LarE55 embryos.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Suppressor of
    Statement
    Reference
    Phenotype Manifest In
    Enhanced by
    Statement
    Reference

    Larbypass has anterior fascicle & axon | ectopic phenotype, enhanceable by Sdc48

    Larbypass has anterior fascicle & axon | ectopic phenotype, enhanceable by SdcKG06163

    Larbypass has anterior fascicle & axon | ectopic phenotype, enhanceable by Sdc10608

    NOT Enhanced by
    Statement
    Reference

    Larbypass has anterior fascicle & axon | ectopic phenotype, non-enhanceable by Fkbp1400734

    Larbypass has anterior fascicle & axon | ectopic phenotype, non-enhanceable by dally06464

    Larbypass has anterior fascicle & axon | ectopic phenotype, non-enhanceable by dlp1

    Larbypass, dlpA187 has anterior fascicle & axon | ectopic phenotype, non-enhanceable by dally80

    Larbypass, dally80 has anterior fascicle & axon | ectopic phenotype, non-enhanceable by dlpA187

    Larbypass has anterior fascicle & axon | ectopic phenotype, non-enhanceable by Sara250

    Suppressed by
    Suppressor of
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    The following mutations do not increase the frequency of the Larbypass ISNb bypass phenotype: Sara250, Fkbp1300734, dally06464, and dlp1. The Larbypass ISNb phenotype is also not enhanced in Larbypass; dlpA187, dally80 triple mutants.

    Sdc alleles (Sdc10608, SdcKG06163 and Sdc48 in which Sara is rescued by the SaraUbi.PJ transgene) increase the penetrance of the Larbypass ISNb bypass phenotype by more than 2-fold.

    The midline crossing errors seen in the central nervous system of Abl2/Abl2 embryos are suppressed by Larbypass/Larbypass.

    The Larbypass/Larbypass and Larbypass/Lar13.2 ISNb "bypass" phenotype is suppressed by Abl1. The Larbypass/LarE55 ISNb "bypass" phenotype is suppressed by Abl1, Abl2 or Abl4. The ISNd bypass phenotype of Larbypass/LarE55 embryos is also suppressed by Abl1.

    Mutation causes synergy of the Scer\GAL4elav-C155, Rac1N17.Scer\UAS full ISNb bypass phenotype.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments

    Shows phenotypic penetrance of approximately one-third to one-half of Lar null alleles.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (6)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (10)