FB2024_03 , released June 25, 2024
Allele: Dmel\robo1Y-F.UAS
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General Information
Symbol
Dmel\robo1Y-F.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0120360
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-roboY-F
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UAS regulatory sequences drive expression of robo1 containing a Tyr to Phe amino acid replacement in the CC1 domain.

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

At 25-31 hours after egg laying RP2 neuron clones expressing robo1Y-F.Scer\UAS under the control of Scer\GAL4Act5C.PP have a lack of dendritic innervation of the medial neuropile (normally located anterior to the axon) and a concomitant expansion of dendrites in the lateral neuropile posterior to the axon.

At 29oC, 6.1% of abdominal segments have partial or complete transformation of lch5 chordotonal organ morphology towards that of the thoracic dch3 chordotonal organs, in larvae expressing roboY-F.Scer\UAS under the control of Scer\GAL4elav-C155.

Embryos overexpressing roboY-F.Scer\UAS under the control of Scer\GAL4ftz.ng show normal Fas2-axon projections.

Expression of roboY-F.Scer\UAS under the control of Scer\GAL4elav.PLu results in a commissureless phenotype, with no axons crossing the midline.

Expression of roboY-F.Scer\UAS driven by Scer\GAL4unspecified produces a loss of commissure phenotype.

Axons do not cross the midline in embryos expressing roboY-F.Scer\UAS under the control of Scer\GAL4elav.PLu. Three distinct Fas2-expressing longitudinal pathways on each side of the midline are still seen. Expression of roboY-F.Scer\UAS under the control of Scer\GAL4ap-md544 leads to no alteration in the lateral position of the ap-expressing neurons.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Overexpression of roboY-F.Scer\UAS under the control of Scer\GAL4ftz.ng in Abl4 homozygous mutants suppresses the frequency of abnormal crossovers observed in Abl4 mutants.

Overexpression of roboY-F.Scer\UAS under the control of Scer\GAL4ftz.ng in Abl2 homozygous mutants suppresses the frequency of abnormal crossovers observed in Abl2 mutants.

In embryos expressing both Gα49BQ203L.Scer\UAS and roboY-F.Scer\UAS under the regulation of Scer\GAL4elav-C155, ectopic crossovers of the midline by axons.

Many commissural axons cross the midline, with some segments appearing nearly wild type, in embryos coexpressing roboY-F.Scer\UAS and Gef64CEP3035 under the control of Scer\GAL4elav.PLu.

The addition of enaGC1/+ significantly suppresses the loss of commissure phenotype seen in roboY-F.Scer\UAS, Scer\GAL4unspecified flies.

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 (3)
Reported As
Symbol Synonym
robo1Y-F.Scer\UAS
robo1Y-F.UAS
roboY-F.Scer\UAS
Name Synonyms
Secondary FlyBase IDs
    References (7)