FB2024_03 , released June 25, 2024
Allele: Dmel\trioUAS.cBa
Open Close
General Information
Symbol
Dmel\trioUAS.cBa
Species
D. melanogaster
Name
Saccharomyces cerevisiae UAS construct a of Bateman
FlyBase ID
FBal0117278
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-Trio
Key Links
Nature of the Allele
Progenitor genotype
Carried in construct
Cytology
Description

Full length wild type trio cDNA is expressed under the influence of UAS regulatory sequences.

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

Overexpression of a single copy of trioScer\UAS.cBa during eye development driven by Scer\GAL4GMR.PFa causes a mild rough-eye phenotype, and expression of two copies results in a reduced number of ommatidia and a smaller bar shaped eye.

Pan-neuronal expression of trioScer\UAS.cBa under the control of Scer\GAL4elav-C155 does not produce any dominant axon patterning defects in a wild-type background.

Third instar larvae expressing trioScer\UAS.cBa in motor neurons under the control of Scer\GAL4BG380 show a similar number of boutons per muscle surface area as in wild type.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference

Scer\GAL4GMR.PFa, trioUAS.cBa has visible phenotype, enhanceable by kst[+]/kst1

Scer\GAL4GMR.PFa, trioUAS.cBa has visible phenotype, enhanceable by kst[+]/kst2

Scer\GAL4GMR.PFa, trioUAS.cBa has visible phenotype, enhanceable by kst[+]/kstB1-14.1

NOT Enhanced by
Statement
Reference
NOT suppressed by
Statement
Reference
Enhancer of
Statement
Reference
Suppressor of
NOT Suppressor of
Phenotype Manifest In
Enhanced by
Statement
Reference

Scer\GAL4GMR.PFa, trioUAS.cBa has eye phenotype, enhanceable by kst[+]/kst1

Scer\GAL4GMR.PFa, trioUAS.cBa has eye phenotype, enhanceable by kst[+]/kst2

Scer\GAL4GMR.PFa, trioUAS.cBa has eye phenotype, enhanceable by kst[+]/kstB1-14.1

NOT Enhanced by
Statement
Reference
NOT suppressed by
Statement
Reference
Enhancer of
Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The stalling of the ISNb motor nerve at the junction of muscles 6 and 13 with failure to innervate muscle 12 characteristic for Abl4 homozygous mutant embryos is not suppressed by Scer\GAL4elav.PU-driven expression of trioScer\UAS.cBa in the mutant background.

Expression of trioScer\UAS.cBa under the control of Scer\GAL4Act.PU in RhoGAP100FCD R7 photoreceptor cell clones almost completely suppresses the failure of the axon terminals to contact the M6 layer of the medulla. The later tendency for R7 axons that do reach the M6 layer to project extensions is partially suppressed.

Expression of trioScer\UAS.cBa under the control of Scer\GAL4Act.PU in Lar2127 R7 photoreceptor cell clones partially suppresses the failure of the axon terminals to contact the M6 layer of the medulla.

Heterozygosity for kst1 significantly enhances the rough-eye phenotype induced by overexpression of trioScer\UAS.cBa via Scer\GAL4GMR.PFa.

Heterozygosity for kst2 significantly enhances the rough-eye phenotype induced by overexpression of trioScer\UAS.cBa via Scer\GAL4GMR.PFa.

Heterozygosity for kstB1-14.1 significantly enhances the rough-eye phenotype induced by overexpression of trioScer\UAS.cBa via Scer\GAL4GMR.PFa.

Co-expression of kstΔ.Scer\UAS with trioScer\UAS.cBa under the control of Scer\GAL4GMR.PFa does not modify the eye phenotype of trioScer\UAS.cBa-overexpression alone.

Co-expression of kstβH33.Scer\UAS and trioScer\UAS.cBa under the control of Scer\GAL4GMR.PFa suppresses the roughness of both the kstβH33.Scer\UAS and the trioScer\UAS.cBa eye phenotype.

Co-expression of trioScer\UAS.cBa with kstβH33.Scer\UAS under the control of Scer\GAL4ey.200.Exel suppresses the eye phenotype resulting from the overexpression of kstβH33.Scer\UAS.

A trio123.4 heterozygous background significantly restores the ability of ISNb axons to enter the ventrolateral muscle field in Nl1N-ts1 mutants. This suppression is reverted upon pan-neural expression of trioScer\UAS.cBa under the control of Scer\GAL4elav-C155.

Scer\GAL4how-24B- or Scer\GAL4elav-C155-mediated expression of trioScer\UAS.cBa restores the number of boutons in Liprin-βΔ83 animals to control levels.

Scer\GAL4elav-C155-mediated expression of trioScer\UAS.cBa restores the number of boutons in Liprin-αoos animals to control levels.

Expression of trioScer\UAS.cBa in motor neurons under the control of Scer\GAL4BG380 partially suppresses the reduced bouton number phenotype seen in Mad1/Madk00237 larval neuromuscular junctions.

Expression of trioScer\UAS.cBa in motor neurons under the control of Scer\GAL4BG380 partially suppresses the reduced bouton number phenotype seen in witA12/witHA3 larval neuromuscular junctions.

Expression of trioScer\UAS.cBa under the control of either the Scer\GAL4arm.PS or the Scer\GAL4αTub84B.PL driver cannot suppress the semi-lethality seen in vav2 male homozygotes.

Expression of trioScer\UAS.cBa under the control of either the Scer\GAL4arm.PS or the Scer\GAL4αTub84B.PL driver cannot suppress the semi-lethality seen in vav3 male homozygotes.

The border follicle cell migration defect seen in egg chambers expressing Rac1N17.Scer\UAS under the control of Scer\GAL4slbo.2.6 is partially suppressed by coexpression of trioScer\UAS.cBa.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of trioScer\UAS.cBa in neurons under the control of Scer\GAL4OK6 rescues the reduction in synaptic bouton phenotype seen in trioS137203/trio6A third instar larvae. Expression of trioScer\UAS.cBa in muscles using Scer\GAL4G14 is unable to rescue the phenotype.

Expression of trioScer\UAS.cBa only in the larval stages using the neuronal driver Scer\GAL4elav.Switch.PO rescues the reduction in synaptic bouton phenotype seen in trioS137203/trio6A third instar larvae.

When expression is driven by Scer\GAL4T155, wing posture of trioS138606/Df(3L)Ar12-1 is substantially rescued. When expression is driven by Scer\GAL4elav-C155, larval lethality is rescued to pupal lethality. When expression is driven by Scer\GAL4elav-C155, short stop phenotype of ISNb is reduced and short stop phenotype of SNa is eliminated.

Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
trioScer\UAS.cBa
trioUAS.cBa
Name Synonyms
Saccharomyces cerevisiae UAS construct a of Bateman
Secondary FlyBase IDs
    References (12)