FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\MhcR759E
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General Information
Symbol
Dmel\MhcR759E
Species
D. melanogaster
Name
FlyBase ID
FBal0264556
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
PwMhcR759E
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

A R759E amino acid substitution has been introduced into the wild type Mhc sequence in Mhc+t24.1.

Allele components
Component
Use(s)
Regulatory region(s)
Encoded product / tool
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

Two to three day old Mhc10 mutant females expressing MhcR759E.t12.4 exhibit impaired flight ability compared with control flies. The mutant flies are able to take off appropriately, however, they are unable to remain airborne for more than a few seconds and land promptly. About twice as many mutant as control flies either are unable or refused to beat their wings when flight tested. Compared with controls, mutant flies display decreased muscle length amplitude, power generation and optimum frequency of muscle oscillation. No significant differences are observed for active, passive or net tension between mutant and control fibers. Complex stiffness of the mutant muscle fibers is reduced relative to wild-type. The mutants also display some decrease in certain components of mechanical rate constants.

At the late pupal stage, myofibril structure appears normal in homozygous Mhc10 mutants expressing MhcR759E.t12.4, with normal thick and thin filament arrangements and intact sarcomeres. This is true for adults at 2 h after eclosion. At 2 days of age, sarcomere structure is generally normal, but occasional cracks in the mutant myofilament lattice occur. At 1 week after eclosion, mutant myofibrils show moderate to severe disruption. Hexagonal packing of filaments is not as regular as it is in wild-type, with gaps in the myofilament lattice. Thus, while mutant muscle assembly appears normal, myofibrils degenerate as flies age. Flight ability is severely

impaired in young Mhc10 mutants expressing MhcR759E.t12.4, and it deteriorates as flies age.

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
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
MhcR759E.t12.4
MhcR759E
Name Synonyms
Secondary FlyBase IDs
    References (3)