FB2024_03 , released June 25, 2024
Allele: Dmel\Drice17
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General Information
Symbol
Dmel\Drice17
Species
D. melanogaster
Name
FlyBase ID
FBal0219086
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: N116Y.

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

A29800243T

Amino acid change:

N116Y | Drice-PA

Reported amino acid change:

N116Y

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

In Drice17 mutants, the number of apoptotic cells in the optic lobe is greatly increased at 24h APF, and remains increased compared to wild type through late pupal stages. Cell corpse clearance is greatly reduced in several regions of the optic lobe, but is normal in other regions.

The programmed cell death of bursCCAP neurons seen in the adult ventral nerve cord of wild type flies after eclosion is suppressed in Ice17 mutant homozygotes. On average 10 bursCCAP cells are seen per tissue at 3-5 days.

The programmed cell death of bursCCAP neurons seen in the adult ventral nerve cord of wild type flies after eclosion is strongly suppressed in IceΔ1/Ice17 mutants; six bursCCAP neurons survive in 3-5 day old flies.

Ice17/IceΔ1 trans-heterozygous mutants exhibit a reduction in dendritic branch pruning at 18 hours after puparium formation.

Only approximately one-third of the expected number of homozygotes are recovered. The lethal phase occurs during embryogenesis without a detectable phenotype.

Homozygous flies have wings that appear less transparent compared to wild type.

Cell death is significantly reduced compared to wild type in homozygous embryos lacking both zygotic and maternal Ice function. Stage 17 mutant embryos have contain on average more than twice the number of midline glia cells compared to wild-type controls.

Apoptosis in the eye disc at 26 hours after puparium formation (APF) is reduced in mutants compared to wild type. At 42 hours APF the homozygous clones in the eye disc contain on average 1.6 +/- 0.75 additional interommatidial cells compared to wild-type controls. In rare cases, a bristle cell is replaced by a tertiary pigment cell.

Fewer apoptotic cells are induced after irradiation in mutant embryos compared to wild type.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference
Suppressor of
Statement
Reference

DriceΔ1/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceL1/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceL2/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceC1/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceC2/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceS1/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceS2/Drice17 is a suppressor of visible phenotype of hidGMR.PG

DriceΔ1/Drice17 is a suppressor of visible phenotype of rprGMR.PW

Df(3R)Drice/Drice17 is a suppressor of visible phenotype of hidGMR.PG

Drice17/Drice17 is a suppressor of visible phenotype of rprGMR.PW

NOT Suppressor of
Statement
Reference

Drice[+]/Drice17 is a non-suppressor of visible phenotype of hidGMR.PG

Drice[+]/Drice17 is a non-suppressor of visible phenotype of rprGMR.PW

Drice17/Drice17 is a non-suppressor of visible phenotype of Dcp-1ΔN.GMR

Other
Phenotype Manifest In
Suppressor of
Statement
Reference

DriceΔ1/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceL1/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceL2/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceC1/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceC2/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceS1/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceS2/Drice17 is a suppressor of eye phenotype of hidGMR.PG

DriceΔ1/Drice17 is a suppressor of eye phenotype of rprGMR.PW

Df(3R)Drice/Drice17 is a suppressor of eye phenotype of hidGMR.PG

Drice17/Drice17 is a suppressor of eye phenotype of rprGMR.PW

NOT Suppressor of
Statement
Reference

Drice[+]/Drice17 is a non-suppressor of eye phenotype of hidGMR.PG

Drice[+]/Drice17 is a non-suppressor of eye phenotype of rprGMR.PW

Drice17/Drice17 is a non-suppressor of eye phenotype of Dcp-1ΔN.GMR

Other
Additional Comments
Genetic Interactions
Statement
Reference

Drice17/Drice17, Drice17/DriceΔ1, Drice17/DriceL1, Drice17/DriceL2, Drice17/DriceC1, Drice17/DriceC2, Drice17/DriceS1, Drice17/DriceS2 (but not Drice17/+) significantly suppresses the eye ablation phenotype in hidGMR.PG flies. Drice17/DriceΔ1 (but not DriceΔ1/+) significantly suppresses the eye ablation phenotype in rprGMR.PW flies. Drice17/+ does not suppress the eye ablation phenotype in rprGMR.PW flies.

In Drice17 and Dcp-1Prev1 double mutants, the number of apoptotic cells is reduced compared to wild type between 0-24h APF, and is slightly increased between 48-72h APF.

Homozygous Ice17 clones induced in the eye suppress the eye ablation phenotype caused by WGMR.PG.

The eye ablation phenotype caused by WGMR.PG is suppressed if the flies are also carrying Ice17/Ice17 or Ice17/Df(3R)Ice.

The eye ablation phenotype caused by rprGMR.PW is weakly suppressed by homozygosity for Ice17.

Ice17 Dcp-1Prev1 double mutant embryos derived from mutant female germline clones (so lacking maternal and zygotic function of Ice and Dcp-1 show significantly reduced levels of apoptosis compared to Ice17 single maternal and zygotic mutant embryos, containing only a few dying cells.

Homozygosity for Ice17 does not suppress the apoptosis induced in the third larval instar eye disc by expression of either Ncpro.Scer\UAS or NcΔN.Scer\UAS under the control of Scer\GAL4GMR.PU.

The "spotted" eye phenotype caused by Dcp-1ΔN.GMR is not suppressed by homozygosity for Ice17.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
References (13)