FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Syt1P-L.UAS
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General Information
Symbol
Dmel\Syt1P-L.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0337196
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
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 Syt1 cDNA with an amino acid replacement (P363L); this proline residue is homologous to proline 308 in human syt2, which has been associated with human congenital myasthenic syndrome.

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 ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
This allele represents a human variant implicated in disease.
SYT2:p.Pro308Leu
Variants Synonym(s)
Associated human disease model(s)
External database links
Comments concerning this variant
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Syt1AD4 homozygotes are partially lethal and the rate of their lethality is further increased by Scer\GAL4elav.PU-driven expression of Syt1P-L.Scer\UAS.

Syt1AD4 heterozygotes expressing Syt1P-L.Scer\UAS (with Scer\GAL4elav.PU) have reduced adult lifespan (compared to flies expressing Syt1Scer\UAS.cSb), at third instar larval stage the neural transmission at neuromuscular junction is impaired: the excitatory junction potential (EJP) amplitude is decreased but the amplitude as well as frequency of miniature EJP is unaffected as is the size of readily releasable pool of synaptic vesicles. However, the Syt1P-L.Scer\UAS-expressing larvae also display significant decrease in the Ca[2+] affinity of release and larger paired pulse ratio, indicating a reduction in release probability, following either 10Hz or 50Hz train stimulation for 2sec, a significant decrease in synaptic depression is observed relative to controls but when a single stimulus is applied again 1 minute after the end of the stimulus train this effect is no longer evident. Syt1AD4,Scer\GAL4elav.PU/+;Syt1P-L.Scer\UAS adults show reduced locomotor activity compared to age- and sex-matched controls but the circadian pattern of their activity is comparable to the Syt1Scer\UAS.cSb-expressing controls, the mutants also show faster rate of muscle fatigue (measured in a modified climbing assay).

External Data
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
Fails to rescue
Comments

The partial lethality of Syt1AD4 homozygotes is not only rescued by Scer\GAL4elav.PU-driven expression of Syt1P-L.Scer\UAS but the lethality rate is further increased.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Syt1P-L.Scer\UAS
Syt1P-L.UAS
Name Synonyms
Secondary FlyBase IDs
    References (2)