FB2024_03 , released June 25, 2024
Allele: Dmel\Src42ACA.UAS
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General Information
Symbol
Dmel\Src42ACA.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0103957
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-Src42ACA, UAS-Src42A.CA, UAS-Src42CA, Src42ACA, UAS-Src42AYF, UAS-Src42A-CA
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 a constitutively active form of Src42A (carries the amino acid replacement Y511F), with the mutation described above.

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 ( 1 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
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

Expressing Src42ACA.UAS under the control of Scer\GAL4GMR.PF leads to massive defects in eye development when flies are raised at 25[o]C, but only mild defects at 18[o]C. At 18[o]C a significant proportion of CadN-immunopositive adherens junctions between photoreceptor precursor cells R3 and R4 in row 5 ommatidia of wandering third instar larvae are shorter compared to controls.

Adult flies expressing Src42ACA.Scer\UAS driven by Scer\GAL4esg-NP7397 combined with tub-Gal80[ts] (for temporal control) display significant increase in midgut stem cell proliferation (assessed by number of pH3-positive cells).

In the tracheal dorsal trunk of stage 17 embryos, expression of Src42ACA.UAS under the control of Scer\GAL4btl.PS leads to disruption of taenidial fold structure and F-actin bundling when compared to controls.

Scer\GAL4esg-NP5130-mediated expression of Src64BScer\UAS.cCa (restricted to adult stages by using P{tubP-GAL80ts}) results in substantial intestinal stem cell hyperproliferation and hyperplasia of the adult intestine.

Expression of Src42AScer\UAS.cPa under the control of Scer\GAL4btl.PS results in over-elongated and convoluted dorsal trunks. Dorsal trunk metameres are 23% longer than in controls although dorsal trunk cell number is unchanged. Cells are flattened and markedly elongated axially.

Expression of Src42ACA.Scer\UAS under the control of Scer\GAL4btl.PS causes disintegration of the tracheal epithelium. Tracheal cell contacts persist but becomes loose, cells become rounded and the lumen becomes discontinuous. Dorsal branch tip cells occasionally become detached, and in some cases tracheal cells that are detached from one branch re-attach to a neighbouring branch. Tracheal cells fail to stabilise cell junctions and to extend dorsal branches, although they retain filopodia activity.

When Src42ACA.Scer\UAS is driven by Scer\GAL4slbo.2.6 in the follicle cells, an increase is seen in the accumulation of F-actin. These cells also show a disruption of the normal cell shape. Border cell migration is completely blocked.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhanced by
Suppressed by
NOT suppressed by
Phenotype Manifest In
Enhanced by
NOT Enhanced by
Suppressed by
NOT suppressed by
Suppressor of
Statement
Reference
NOT Suppressor of
Additional Comments
Genetic Interactions
Statement
Reference

The increased number of intestinal progenitor cells in mitosis characteristic for adult flies expressing Src42ACA.Scer\UAS driven by Scer\GAL4esg-NP7397 (combined with tub-Gal80[ts] for temporal control) is suppressed by co-expression of RetGD45.

One copy of shg2 enhances the tracheal epithelium defects seen when Src42ACA.Scer\UAS is expressed under the control of Scer\GAL4btl.PS. The dorsal trunk is broken in many places and cells are more rounded. Expressing Src42ACA.Scer\UAS in a homozygous shg2 background results in complete cell dissociation.

Expression of shgScer\UAS.T:Avic\GFP-rs partially suppresses the tracheal defects seen when Src42ACA.Scer\UAS is expressed under the control of Scer\GAL4btl.PS. Tracheal cells maintain apico-basal polarity for at least two hours longer than when Src42ACA.Scer\UAS is expressed alone, and dorsal branch extension is also partially restored.

Expression of panΔN.Scer\UAS enhances the tracheal phenotype seen when Src42ACA.Scer\UAS is expressed under the control of Scer\GAL4btl.PS. Tracheal cells lose polarity and dissociate from the epithelium.

Expression of either the activated Src42ACA.Scer\UAS transgene fails to rescue DokPG155 germ-line clone embryos.

When Src42ACA.Scer\UAS is driven by Scer\GAL4slbo.2.6 in a homozygous Cortactinunspecified background, a small but significant suppression is seen in the F-Actin phenotype.

The mutant dorsal appendage phenotype seen in bwk151/bwk08482 eggs is suppressed by expression of Src42ACA.Scer\UAS under the control of Scer\GAL4c415.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Src42ACA.Scer\UAS
Src42ACA.UAS
Name Synonyms
Secondary FlyBase IDs
    References (29)