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General Information
Symbol
Dmel\mbcC1
Species
D. melanogaster
Name
FlyBase ID
FBal0044174
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
mbc1
Key Links
Nature of the Allele
Mutations Mapped to the Genome
 
Type
Location
Additional Notes
References
Associated Sequence Data
DNA sequence
Protein sequence
 
 
Progenitor genotype
Cytology
Nature of the lesion
Statement
Reference
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

mbcC1/mbcD11.2 transheterozygote embryos display defects in the migration of the visceral longitudinal muscle founder cells and their morphology as well as the muscle fusion. Late in the embryonic development, the first midgut constriction is missing in the mbcC1/mbcD11.2 mutants.

Mutant embryos show decelerated and irregular outgrowth of the visceral mesoderm. Many unfused myoblasts surround the visceral mesoderm in the mutant embryos.

mbcC1 mutants show enlarged foci, as well as increased numbers of actin foci. Enlarged foci are seen in these mutants from the earliest stages of fusion and foci persist after fusion would be complete in wild-type.

In mbcC1 mutant embryos, the secretory star cells (stellate cells) integrate into the developing Malpighian tubule epithelium but are reduced in number. The tubules themselves exhibit severe misguidance defects. Tha anterior tubules are shortened and knotted.

Homozygous embryos do not show any apparent defects in macrophage migration.

No somatic muscle cell fusion occurs in mbcC1 mutant embryo, leaving only mononucleated myoblasts.

In mutant embryos, syncytia within somatic muscles are almost absent. Mutants show defects in the formation of midgut constrictions, and show severe abnormalities in the formation of visceral muscles. At stage 12 the visceral band is randomly interrupted and the elongated Fas3 expressing cells seem to be disorientated. During further development parts of the visceral band either stretch out in the dorsal ventral direction (as in wild-type) or form disarranged patches. The number of myoblast founder cells appears to be reduced, and large gaps are visible in the visceral band. Many globular cells are seen at the margin of the visceral band that appear to be unfused myoblasts. No myoblast fusion is detectable. While the circular musculature shows severe defects and is apparently reduced, the longitudinal musculature is completely absent at the end of embryogenesis.

Syncytia are not seen in the midgut musculature of mutant embryos. Two classes of fibres are apparent (as in wild type) - elongated, longitudinal cells and smaller circular fibres at right angles to them, but in contrast to wild type these fibres are mononucleate in mutant embryos. Elongated circular muscle founder cells and unfused myoblasts become closely apposed in the visceral mesoderm of developing embryos, but them fail to fuse.

The development of multinucleate muscles is blocked in mutant embryos, but tendon cells are specified normally.

Myoblasts fail to fuse and form loose clusters of cells in locations roughly corresponding to the ventral, lateral and dorsal muscle groups. They are in random orientation relative to pioneer cells. Myoblasts exhibit near complete absence of prefusion complexes, an occasional complex can be seen at apparently random locations. The complex is wild type, showing no defects. Most unfused cells are cleared by macrophages by the end of stage 16.

Embryos homozygous for the mbcC1 chromosome (or heterozygous for mbcC1 and Df(3R)mbc-R1), show a variably expressed 'dorsal open' phenotype.

Fusion of myoblasts to form myotubes is virtually absent (development of syncytial muscles is blocked), but muscle founder cells form and later elongate, make epidermal contacts and develop into mononucleate muscles that express differentiated muscle markers. Limited number of neuromuscular synapses form and their ultrastructure is identical to the wild type, EJCs demonstrate the junctions are functional.

Embryos lie motionless in the vitelline membrane and fail to hatch. Examination with polarised light reveals a lack of differentiated muscle. Myoblasts fail to fuse. At 13 to 14 hours of development the myoblasts lie in a segmental array. At 16 to 17 hours of development the myoblasts fall into two populations, stretched and rounded. Stretched myoblasts first appear at around 11 hours after egg laying, and eventually can span distances two or three times the length of normal muscles. They often occur at positions and in orientations reminiscent of wild type muscle precursors. Only very few fusions occur. Segregation and movement of slou-expressing founder cells and vg-expressing cells is normal.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT Suppressor of
Statement
Reference

mbcC1 is a non-suppressor of phenotype of arm3

Additional Comments
Genetic Interactions
Statement
Reference

prtpΔ1/+ ; mbcC1/+ double heterozygotes show a comparable level of phagocytosis in embryonic hemocytes as in wild-type controls.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

Epidermal development and differentiation are normal.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (21)