FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\fruMB.UAS.cSa
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General Information
Symbol
Dmel\fruMB.UAS.cSa
Species
D. melanogaster
Name
FlyBase ID
FBal0144289
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of fru consisting of sequences encoding the 101 male specific amino terminus and the BTB domain derived from the fru male cDNA nos. 5-19 fused to the "B" 3' end (derived from fru cDNA no. 25).

Allele components
Component
Use(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

Approximately 15% of wild-type females expressing fruMB.Scer\UAS.cSa under the control of Scer\GAL4fru.16 develop on average three ectopic `male' serotonergic neurons, sending projections into the abdominal nerve trunk. Ectopic serotonergic terminals innervated the female internal reproductive organs, mostly the calyx of the ovaries but also, more rarely, the uterus and the base of the spermathecae. These serotonergic terminals are never present in virgin or fertilised wild-type females. The ectopic serotonergic neurons and their associated terminalia are analogous to those innervating the male reproductive organs.

The Fas2-positive and BP102-positive axon tracts in the central nervous system are defective in virtually all fruw12/frusat15 embryos which are expressing fruMB.Scer\UAS.cSa under the control of Scer\GAL4sca-537.4.

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

Expression of fruMB.Scer\UAS.cSa, under the control of Scer\GAL4fru.16 in a fru3/fru3 background does not restore male fertility.

Expression of fruMB.Scer\UAS.cSa under the control of Scer\GAL4fru.16 fails to rescue fertility levels in fru3/fruΔC mutants.

Expression of fruMB.Scer\UAS.cSa under the control of Scer\GAL4fru.16, in fru3 homozygotes and fru3/fruΔC transheterozygotes fails to rescue the formation of the muscle of Lawrence in the male and fails to induce formation of muscle of Lawrence-like features and neuromuscular junctions in the female.

Expression of fruMB.Scer\UAS.cSa under the control of Scer\GAL4fru.16 in fruΔC/fru3 mutants induces differentiation of neurons in the dorsal serotonergic abdominal giant neurons, with up to five neurons (half the wild-type number) developing per animal. Rescue in the ventral serotonergic abdominal giant neurons is not observed.

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
fruMB.Scer\UAS.cSa
fruMB.UAS.cSa
Name Synonyms
Secondary FlyBase IDs
    References (4)