FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Tpisgk-js10
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General Information
Symbol
Dmel\Tpisgk-js10
Species
D. melanogaster
Name
FlyBase ID
FBal0195201
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
TpiJS10, TPInull
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Cytology
Description

Imprecise excision of the P{EPgy2} element, resulting in a 1.6kb deletion that removes most of the Tpi gene (nucleotides -319 to +1288 relative to the start of exon 1 are missing).

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

1.6 kb deletion resulting from the imprecise excision of the P{EPgy2}TpiEY03361 element. The deletion extends from -319 to +1288 relative to the start of exon 1.

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 )
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

TpiR187K/Tpisgk-js10 and TpiM80T/Tpisgk-js10 individuals are bang sensitive.

TpiM80T/Tpisgk-js10 transheterozygous adults exhibit a significant decrease in lifespan, an increase in heat sensitivity, shown by the significant decrease in the time until paralysis after 38[o]C temperature shift, and an increase in bang sensitivity, shown by a significant increase in recovery time from mechanical stress, as compared to controls.

The presence of one copy of Hsap\TPI1M82T.Tpi (in which the coding sequence of endogenous Tpi is replaced by the human ortologue bearing the M82T amino-acid substitution), but not of one copy of Hsap\TPI1Tpi.WT (in which the coding sequence of endogenous Tpi is replaced by the human ortologue bearing the M82T amino-acid substitution), in a Tpi-null background (TpihTPI.M82T/Tpisgk-js10 or TpihTPI.WT/Tpisgk-js10, respectively) leads to adult exhibiting a small decrease in lifespan, a small increase in bang sensitivity, shown by a small but significant increase in recovery time from mechanical stress, and an increase in heat sensitivity, shown by the significant decrease in the time until paralysis after a temperature shift to 38[o]C, as compared to controls.

Compared to Tpisgk-js10/TpihTPI.WT control heterozygotes, Tpisgk-js10/TpihTPI.I170V flies (both 3-4 and 20-22 days old) are more sensitive to mechanical- (significant increase in recovery time) and thermal- (significant decrease in time to paralysis) stress, but do not show significant changes in lifespan.

Ratios of redox molecules are significantly shifted towards the oxidised form in Tpisgk-1/Tpisgk-js10 animals compared to controls. This phenotype is age-dependent.

Tpisgk-1 homozygotes and Tpisgk-1/Tpisgk-js10 flies show a delay in recovery after mechanical stress compared to controls, at both 3 and 20 days of age.

Tpisgk-1 homozygotes and Tpisgk-1/Tpisgk-js10 flies show paralysis upon thermal stress, at both 3 and 20 days of age.

Tpisgk-1 homozygotes and Tpisgk-1/Tpisgk-js10 flies show significantly reduced median longevity compared to controls.

Homozygotes do not survive beyond larval stage 2.

Tpisgk-1/Tpisgk-js10 flies take longer to regain normal locomotion after mechanical stress than control flies. This stress sensitivity is progressive and increases significantly with the age of the flies at all temperatures examined (room temperature, 25oC and 29oC). Severe stress sensitivity is evident much earlier in flies maintained at 25oC or 29oC compared to those raised at room temperature.

Lifespan of homozygous and Tpisgk-1/Tpisgk-js10 animals is significantly reduced compared to controls at room temperature, 25oC and 29oC. The decrease in lifespan compared to controls becomes more severe as the temperature at which the flies are raised is increased.

Young Tpisgk-1/Tpisgk-js10 adults do not show neuropathological defects, however, by their median age, they develop marked neuropathology, showing degeneration in the brain and thoracic ganglion. This degeneration is seen in flies raised at room temperature, 25oC and 29oC.

External Data
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Phenotypic Class
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Xenogenetic Interactions
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Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)