FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\stnA12
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General Information
Symbol
Dmel\stnA12
Species
D. melanogaster
Name
FlyBase ID
FBal0016212
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
stn13-120
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Insertion into ORF1.

Doc element insertion.

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

Mutants die as mature embryos after a failure to hatch, due to lack of coordination. Mutant embryos show normal segmental patterning of the epidermis, muscles and nervous system. Mutant nmjs appear morphologically wild type though the nerve terminals are slightly smaller than normal. In electrophysiological recordings at the embryonic nmj nerve stimulation produces muscle contraction demonstrating that presynaptic depolarization evokes transmitter release and that muscle excitation-secretion response is intact. However evoked EJC peak amplitudes are significantly reduced and the release of neurotransmitter at mutant synapses is markedly asynchronous due to delayed presynaptic vesicle fusion. Mutants have an impaired ability to synchronously trigger calcium-mediated vesicle fusion. The overall level of neurotransmitter release is reduced. Variability in EJC peak amplitudes is increased, compared to wild type. Transmission fidelity is lost. Calcium sensitivity is unaltered. MEJC frequency is not significantly altered, though amplitude is increased, perhaps because of increased quantity of neurotransmitter in some vesicles. Mutant synapses exhibit severe fatigue after prolonged stimulation. Synapses show decreased synaptic vesicle density and accumulate membrane-recycling intermediates.

Flies heterozygous for stnA15 and any of the lethal "stn" alleles show either a small or no off transient in ERGs. Flies heterozygous for a ts and a lethal allele of stnA show ERGs with off transient amplitudes between those for stnA7 and stnA15.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
NOT Enhancer of
Statement
Reference
Other
Statement
Reference

stnA12/stnA6, stnB6/stnB12 has neuromuscular junction & synaptic vesicle phenotype

Additional Comments
Genetic Interactions
Statement
Reference

stnA12 stnB12/Y ("stn13-120") males do not survive to adulthood. The lethality of stnA12 stnB12/Y ("stn13-120") animals is not rescued by expression of sytScer\UAS.cLa under the control of either Scer\GAL4elav-C155 or Scer\GAL4shi.PS.

stnA12 stnB12 ("stn13-120") mutant embryos show a more than 90% reduction in FM1-43 dye uptake at the neuromuscular junction after stimulus compared to wild type. stnA12 stnB12 ("stn13-120") homozygotes show embryonic lethality. Expression of sytScer\UAS.cLa under the control of Scer\GAL41407 in this background results in approximately 98% of animals hatching at normal times, but they then die as first instar larvae. Expression of sytScer\UAS.cLa under the control of Scer\GAL44G in the stnA12 stnB12 background results in approximately 96% of embryos hatching, although hatching is delayed (animals hatch between 21 and 35 hours after fertilisation. These animals show adult viability.

Synaptic vesicle internalisation at the neuromuscular junction is delayed relative to wild type in stnB6/stnB12 mutants.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of the dicistronic P{UAS-stnAB.E} construct (which expresses stnAAB.Scer\UAS and stnBAB.Scer\UAS) under the control of either Scer\GAL4elav-C155 or Scer\GAL4shi.PS rescues the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of the dicistronic P{UAS-stnAB.E} construct (which expresses stnAAB.Scer\UAS and stnBAB.Scer\UAS) under the control of Scer\GAL4Mhc.PW does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnBScer\UAS.cEa under the control of Scer\GAL4elav-C155 rescues the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnBScer\UAS.cEa under the control of Scer\GAL4Mhc.PW does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals. Expression of stnAScer\UAS.cEa under the control of Scer\GAL4elav-C155 does not rescue the lethality of stnA12 stnB12/Y ("stn13-120") animals.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Schalet.

Comments
Comments

Used in mosaic analysis to show that the "stn" product is not required for all cell types, but is required in the head for normal active behavior and in the thorax for motor coordination and posture.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
References (11)