FB2024_03 , released June 25, 2024
Allele: Dmel\rux3
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General Information
Symbol
Dmel\rux3
Species
D. melanogaster
Name
FlyBase ID
FBal0035521
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

The rux3 allele carries a frameshift mutation that encodes a protein with 21 out of frame amino acids after aa 320.

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

The exact nature and location of the mutation were inferred by the FlyBase curator. The mutation is reported as a frameshift mutation that encodes a truncated rux protein with 21 novel amino acids after amino acid 320 but the exact nature of the frameshift mutation was not specified. The mutation was annotated as a 19 bp deletion starting at amino acid 321, which would produce a protein consistent with the reported product.

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

The spatiotemporal pattern of mitotic domains is disrupted during Mitosis 14 of the developing embryo. Metaphase is on average 79% longer in mutants than in wild-type embryos. The other stages of mitosis are not significantly altered in mutant embryos.

Homozygotes exhibit a rough eye phenotype. All cells enter S phase and do so earlier than wild type, some cells establish a G1 phase, albeit shorter in length.

Eyes are rough, viability reduced to 50% with respect to wild type.

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

rux3 has visible phenotype, enhanceable by Ras85De1B

rux3 has visible phenotype, enhanceable by Ras85De2F

rux3 has visible phenotype, enhanceable by S1

rux3 has visible phenotype, enhanceable by ast1

Suppressed by
Statement
Reference

rux3 has visible phenotype, suppressible by CycA3

rux3 has visible phenotype, suppressible by CycA5

rux3 has visible phenotype, suppressible by stgRXT13

rux3 has visible phenotype, suppressible by stgAR2

Phenotype Manifest In
Enhanced by
Statement
Reference

rux3 has eye phenotype, enhanceable by ebiE90

rux3 has eye phenotype, enhanceable by ebiE4

rux3 has eye phenotype, enhanceable by Ras85De1B

rux3 has eye phenotype, enhanceable by Ras85De2F

rux3 has eye phenotype, enhanceable by S1

rux3 has eye phenotype, enhanceable by ast1

Suppressed by
Statement
Reference

rux3 has phenotype, suppressible by swmunspecified

rux3 has phenotype, suppressible by S(rux)2C1

rux3 has phenotype, suppressible by S(rux)2C2

rux3 has phenotype, suppressible by S(rux)2C3

rux3 has phenotype, suppressible by stgS(rux)3A

rux3 has phenotype, suppressible by CycAS(rux)3B

rux3 has phenotype, suppressible by Rca1S(rux)2A

rux3 has eye phenotype, suppressible by CycA3

rux3 has eye phenotype, suppressible by CycA5

rux3 has eye phenotype, suppressible by stgRXT13

rux3 has eye phenotype, suppressible by stgAR2

Enhancer of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

The addition of rux3, prolongs the metaphase arrest phenotype seen in CycAScer\UAS.Δ170,Scer\GAL4prd.RG1 embryos.

The G1 gap is restored when heterozygous for Rca1. swm, S(rux)2C, stg and CycA mutations also suppress cell cycle defects, restores a normal G1 in the morphogenetic furrow.

Mutant eye phenotype of rux3 is dominantly enhanced by Ras85De2F and Ras85De1B, ast1 and S1. Removing a copy of Sos or rl has no effect on the severity of the rux3 mutant phenotype. 81% of ommatidia of rux3 are restored to wild type by CycA3 or CycA5. 36% of ommatidia of rux3 are restored to wild type by stgRXT13 or stgAR2.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Weak rux allele.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (5)