FB2024_03 , released June 25, 2024
Allele: Dmel\SK1
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General Information
Symbol
Dmel\SK1
Species
D. melanogaster
Name
FlyBase ID
FBal0266127
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Cytology
Description

FLP-mediated recombination between SKf07979 and SKf01403 generates a deletion removing the 18 exons of SK encoding the six transmembrane and CAMBD domains.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Comment:

~38 kb deletion generated by FLP-FRT-mediated recombination using PiggyBac insertions PBac{WH}SKf07979 and PBac{WH}SKf01403.

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
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Modifiers Based on Experimental Evidence ( 0 )
Disease
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Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

The slow Ca[2[+]]-activated K[+] current found in photoreceptors is abolished in SK1 mutants.

The current/voltage relationship of SK1 photoreceptors is the same as in wild-type, exhibiting increased conductance with hyperpolarization. This current is not affected by tetraethylammonium application.

In dissociated photoreceptors, 1-Ethyl-2-benzimidazolinone induces a slow Ca[2[+]]-activated K[+] current in wild-type but not in SK1 mutants. However the SK current is not altered by apamin treatment, suggesting that SK is apamin insensitive.

SK1 mutant photoreceptors respond as wild-type to intensified light flashes, with graded transient depolarisation, covering similar ranges. However, SK1 photoreceptors show accelerated kinetics; their responses reach peak amplitudes faster and recover to resting potential earlier.

SK1 eyes consist of highly ordered ommatidia, with intact rhabdomeres, as in wild-type. However, prolonged light exposure results in minor changes in photoreceptor integrity. Bump waveforms in SK1 photoreceptors are indistinguishable from those of wild-type photoreceptors. Macroscopic responses to increasing light intensities are similar in wild-type and mutant photoreceptors and share the same kinetics.

Compared with wild-type, SK1 mutant photoreceptor cells exhibit an approximate 25% reduction inI[[A]] current but normal slow delayed rectifier (I[[KS]]) current.

The input resistance of dark-adapted SK1 photoreceptors is significantly decreased compared to wild-type. This is accompanied by a more depolarized resting potential in the dark. Furthermore, in the dark, when their output shows no oscillations, SK1 photoreceptors are noisier than their wild-type counterparts.

SK1 photoreceptors exhibit reduced input resistance, elevated resting potential, and slow oscillating responses.

Although both wild-type and SK1 large monopolar cells respond to light flashes with graded hyperpolarizations of similar sizes, the responses of mutant large monopolar cells are significantly faster. Approximately 40% of SK1 mutant large monopolar cells show oscillating responses. The oscillations are exacerbated at dim conditions. Longer recordings reveal that the oscillations in mutant cells carry different frequencies during and after light adaption. Furthermore, compared with photoreceptors, these oscillations are larger and faster, peaking at ~100Hz.

External Data
Interactions
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Phenotypic Class
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Additional Comments
Genetic Interactions
Statement
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Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of SKScer\UAS.T:Hsap\MYC under the control of Scer\GAL4Act5C.PU rescues the slow Ca[2[+]]-activated K[+] current in SK1 photoreceptors.

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Synonyms and Secondary IDs (2)
Reported As
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Name Synonyms
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    References (2)