FB2024_03 , released June 25, 2024
Allele: Dmel\singGD3396
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General Information
Symbol
Dmel\singGD3396
Species
D. melanogaster
Name
FlyBase ID
FBal0200033
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
UAS-sing RNAi
Key Links
Genomic Maps

Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

UASt regulatory sequences drive expression of an inverted repeat.

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

Scer\GAL4Mef2.PU singGD3396 pharate adults show a considerable reduction in muscle mass compared to wild type: no skeletal muscles are consistently observed in the mutants, except for small, partially developed dorsal longitudinal muscles. The nuclei in the mutant muscles are often clustered together and always fewer in number compared to the homogenously dispersed nuclei of wild type. These phenotypes are attributed to a myoblast fusion defect at the stage following the formation of F-actin foci.

Expression of singGD3396 in just the muscle founder cells using Scer\GAL4kirre-rP298, or in just the fusion competent myoblasts using Scer\GAL4sns.PK, results in 100% viable adults with normal muscle formation. However, expression of singGD3396 simultaneously in muscle founder cells and fusion competent myoblasts using both Scer\GAL4kirre-rP298 and Scer\GAL4sns.PK is lethal, with pharate muscle showing a clear reduction in the number of nuclei per muscle, indicating reduced myoblast fusion.

Adults expressing singGD3396 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.

Expression under the control of Scer\GAL4Mef2.PR results in late pupal lethality.

Expression under the control of Scer\GAL4pnr-MD237 results in bristle morphology defects on the notum in 20-30% of the Scer\GAL4pnr-MD237 expression domain.

External Data
Bristle Screen Database (Knoblich Lab) - A database for RNAi phenotypes in bristle and notum development
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
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 1 )
Linkouts
Bristle Screen Database (Knoblich Lab) - A database for RNAi phenotypes in bristle and notum development
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
CG13011GD3396
singGD3396
Name Synonyms
Secondary FlyBase IDs
    References (7)