FB2024_03 , released June 25, 2024
Allele: Dmel\KCNQ186
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General Information
Symbol
Dmel\KCNQ186
Species
D. melanogaster
Name
FlyBase ID
FBal0244108
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Imprecise excision of the progenitor insertion, deleting all transmembrane domains including the potassium selective pore region of the KCNQ channel.

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)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

KCNQ186 adults lack the significant decrease in preference for nutritive sugars seen in fed versus starved flies, compared to controls.

Flies homozygous for the KCNQ186 allele have a significant impairment of initial 2 min memory, 1 hour memory and 24 hour memory compared to controls. KCNQ186 homozygotes have no alterations in olfactory acuity or shock reactivity compared to controls.

KCNQ186 mutant larvae take 1-2 days longer to develop, a reduced number of animals eclose, and the mean lifespan of females is reduced by 20-30%. Mutant adults show a drastically increased incidence of pacing-induced cardiac dysfunction compared to age-matched controls, and the elevated failure rates observed in young mutant flies does not increase further with age.

Semi-intact KCNQ186 fly heart preparations from young (1-3 week old) flies exhibit severely nonrhythmic beating patterns, and the incidence of arrhythmia increases more rapidly with age compared to control preparations. A dramatic age-dependent increase of the heart period (defined as the length of time between the ends of two consecutive diastolic intervals) compared with age-matched controls is also observed, and both diastolic intervals and systolic intervals show age-dependent increases in length.

Electrophysiology field potential recordings from semi-intact KCNQ186 fly heart preparations show that negative deflections do not immediately follow the initial positive potentials, and usually occur with significant delay compared to wildtype preparations.

Semi-intact KCNQ186 fly heart preparations show lower rates of muscle contractions compared to controls. In response to electrical stimulation, hearts exhibit fibrillation, markedly elevated diastolic tension, and extremely delayed recovery to baseline diastolic tension relative to wildtype hearts.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of KCNQScer\UAS.cOa under the control of Scer\GAL4how-24B in a KCNQ186 mutant background rescues the increased pacer-induced cardiac dysfunction rates and alterations in rhythmicity to levels comparable to those observed in control animals.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)