FB2024_03 , released June 25, 2024
Allele: Dmel\Vps26B
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General Information
Symbol
Dmel\Vps26B
Species
D. melanogaster
Name
FlyBase ID
FBal0316799
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: K264term.

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

A1875006T

Amino acid change:

K264term | Vps26-PA

Reported amino acid change:

K264term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

Vps261 mutant photoreceptor cells exhibit a progressive loss of ERG amplitudes compared to controls. Upon rearing these flies in the dark, Vps261 mutants exhibit nearly normal ERG responses and the ERG amplitude and on- and off-transients in Vps261 mutant photoreceptor cells are slightly reduced when compared to controls. Newly eclosed Vps261 flies exhibit ommatidia that display an overall wild-type morphology, although rhabdomere loss is observed at low frequency in Vps261 mosaic clones.

In a 12-hour light/dark cycle, Vps261 flies show a loss of on- and off-transients, indicating a loss of synaptic transmission. They also exhibit a reduced depolarisation by 2 day, and a progressive loss of the ERG amplitude with age. At day 21, the light-induced photoreceptor cell depolarisation in Vps261 mutant photoreceptor cells is almost completely absent. Three-week-old dark/dark-reared Vps261 mutants exhibit nearly normal ERG responses, similar to newly eclosed flies. The photoreceptor cell morphology of Vps261 mutants is severely affected in flies kept in light/dark conditions for 21 days.

Vps261 flies raised in a light/dark cycle for 4 days show obvious ultrastructural defects in photoreceptor cells when compared to controls. These defects include a dramatic increase in late endosomes and lysosomes. However, photoreceptor cells in dark-reared Vps261 flies do not show an increased number of late endosomes or lysosomes when compared to controls.

Chronic light exposure (for several days) severely affects the endolysosomal system in Vps261 mutants.

A reduction in dietary vitamin A levels in both Vps261 and control flies leads to a decrease in rhabdomere size. In addition, vitamin A degeneration leads to a very strong suppression in photoreceptor cell degeneration in Vps261 mutants at day 10 in a light/dark cycle.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Vps261 ninaE17 double mutants display significant suppression of the ERG and photoreceptor cell defects seen in Vps261 single mutant flies that have been kept in a 12-hour Light/Dark cycle for 4 days.

Vps261, shi1 double mutants raised at 18[o]C and shifted at eclosion to 24[o]C exhibit suppression of the loss of ERG amplitude found in Vps261 single mutants at day 4 in 12-hour light/dark cycles.

Xenogenetic Interactions
Statement
Reference

Ubiquitous expression of Hsap\VPS26AScer\UAS.T:Ivir\HA1 in Vps261 mutants, under the control of Scer\GAL4Act5C.PU, rescues lethality and the loss of on-off transients and ERG amplitude in these mutants. In addition, Hsap\VPS26AScer\UAS.T:Ivir\HA1 expression fully suppresses the photoreceptor cell degeneration seen in Vps261 mutants.

Ubiquitous expression of Hsap\VPS26BScer\UAS.T:Ivir\HA1 in Vps261 mutants, under the control of Scer\GAL4Act5C.PU, rescues lethality and the loss of on-off transients and ERG amplitude in these mutants. In addition, Hsap\VPS26BScer\UAS.T:Ivir\HA1 expression fully suppresses the photoreceptor cell degeneration seen in Vps261 mutants.

Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (7)
References (7)