FB2024_03 , released June 25, 2024
Allele: Dmel\Zasp52Δ
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General Information
Symbol
Dmel\Zasp52Δ
Species
D. melanogaster
Name
FlyBase ID
FBal0216874
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
Nature of the Allele
Associated Insertion(s)
Cytology
Description

Recombination between the Scer\FRT sites in the PBac{WH}Zaspf04847 and PBac{WH}Zaspf04784 insertions has resulted in a deletion that removes exons 5-9 and produces a frameshift.

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

12% of homozygotes die as embryos, while the majority of homozygotes die as first instar larvae. Most of the mutant larvae die within 24 hours of hatching. Those that survive longer never progress beyond the first larval instar (as shown by their small size and mouth hook morphology). Muscle contractions are slower in ZaspΔ larvae compared to wild type.

43% of ZaspΔ/Df(2R)Jp1 animals die as embryos, while the majority die as first instar larvae.

Late stage 17 ZaspΔ embryos lack the typical striated muscle pattern, indicating a Z line defect.

In freshly hatched ZaspΔ larvae, Z lines are either completely absent or are severely disorganised and irregularly spaced in ultrastructural analysis of the muscles. The filaments of the muscles are also disorganised and are no longer arranged in parallel arrays.

Muscle detachment defects are seen from stage 16 onwards in ZaspΔ embryos; the muscle fibers detach from myotendinous junctions. Some muscles are missing in some segments. Late stage 17 embryos occasionally show severe muscle detachment and rounding up of muscles. The muscle detachment is progressive (12% of embryos have rounded muscles at stage 17, but 98% of unhatched embryos have rounded muscles when analysed 24 hours later).

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The muscle detachment phenotype seen in ifSEF embryos is more severe and appears at an earlier stage if the embryos also carry ZaspΔ/+.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Zasp52ZCL423 complements Zasp52Δ in lethal complementation and climbing tests.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

"zaspΔ9" and "zaspΔ56" are independent isolates of an identical mutation, produced by recombination between the Scer\FRT sites in the PBac{WH}Zaspf04847 and PBac{WH}Zaspf04784 insertions.

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