FB2025_01 , released February 20, 2025
Allele: Dmel\Mef2P544
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General Information
Symbol
Dmel\Mef2P544
Species
D. melanogaster
Name
FlyBase ID
FBal0044935
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Caused by aberration
Cytology
Description

Part of the gene is deleted.

Deletion extends from the original site of insertion of P{lArB}MB2487, at approximately 25kb upstream of the 5' end of the Mef2 transcription unit, to 320bp upstream of the start of Mef2 transcription such that the proximal end of the P{lArB} is inserted into the Mef2 promoter.

Allele components
Component
Use(s)
Inserted element
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

The wavy morphology of the dorso-ventral muscle myofibrils of pupae expressing Mef2GD5039 under the control of Scer\GAL4Act88F.PB is worsened if the animals also carry Mef2P544.

20% of Mef2P544/+ flies show defects in TDT organization but all Mef2P544/+ flies show a wild-type number of DLM fibers.

Muscle founder cells never differentiate to form mononucleate muscles. Con, vg or Fas3-expressing founder cells show that target recognition takes place and motoneurons that establish contact are always attracted to the correct founder cells. Myoblast fusion and Mhc and βTub60D expression are severely affected, thus general features of differentiated muscle are deranged or missing. Normal neuromuscular junctions are wholly absent.

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

Mef2[+], brnpr-3, Mef2P544, br[+] is an enhancer of mesothoracic tergotrochanter muscle cell phenotype of twi1

Mef2[+], twi1, Mef2P544, twi[+] is an enhancer of mesothoracic tergotrochanter muscle cell phenotype of brnpr-3

Other
Additional Comments
Genetic Interactions
Statement
Reference

While both twi1/+, Mef2P544/+ and brnpr-3/+; Mef2P544/+ double mutants show a wild-type number of DLM fibers, brnpr-3/+; twi1/+, Mef2P544/+ triple mutants show a reduced numbers of these fibers (5.2 vs 6 in wild type).

brnpr-3/+; Mef2P544/+ double heterozygotes display higher levels of defects in TDT organization than either single heterozygote, including the presence of ectopic fibers in the lumen. twi1/+, Mef2P544/+ also show an increase in the number of TDT defects compared to single mutants. 82% of brnpr-3/+; twi1/+, Mef2P544/+ triple mutants show defects in TDT patterning (a higher level than any of the double mutant combinations), including additional small cells, internal fibers and the rerouting of some fibers to the periphery.

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
Name Synonyms
Secondary FlyBase IDs
    References (10)