FB2024_03 , released June 25, 2024
Allele: Dmel\Orc3lE344
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General Information
Symbol
Dmel\Orc3lE344
Species
D. melanogaster
Name
FlyBase ID
FBal0032074
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
latle344
Key Links
Nature of the Allele
Associated Insertion(s)
Cytology
Description

Deletion from inside P{wd19.3} to somewhere between the 3' end of intron e and the 5' end of intron f. 28bp deletion in intron d as for latP1.

Generated by excision of P{wd19.3} in latP1. Associated with small deletion.

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 at pupal stage P3. Third instar larvae lack imaginal discs and show an undersized CNS. The gross morphology of imaginal discs and CNS in second instar larvae appears normal. No BrdU incorporation is seen in third instar brains, reflecting lack of cell proliferation, whereas 2nd instar brains appear normal.

Homozygous first and second instar larvae show normal morphology and locomotor/feeding behaviour. Third instar larvae show progressively less vigorous locomotion and feeding. Many mutants grow to normal size but remain in the food past the normal wandering stage and delay pupation for several days beyond the normal period. Neuromuscular morphology of mutants shows only minor alterations. Terminal branching pattern is similar to wild type, however mutants have 20% fewer terminal branches, due to fewer higher order branch segments at mutant terminals (assayed at muscle 12). This results in similarly reduced numbers of boutons on muscle 12 and 6/7, but not muscle 4. Mutant EJC amplitudes (muscle 12 and muscle 6) are significantly larger than wild type at all Ca2+ concentrations. mEJCs display no significant differences in mean amplitude, variability, spontaneous frequency or current decay kinetics compared to wild type. Short term synaptic facilitation, synaptic augmentation and posttetanic potentiation are strongly impaired in mutants. Synaptic plasticity defects are incompletely restored by reducing basal transmitter release.

Decrement in 15-minute memory retention.

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
Comments

Complementation statement based on recessive pupal lethality phenotype.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)