FB2024_03 , released June 25, 2024
Allele: Dmel\PolD3L2
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General Information
Symbol
Dmel\PolD3L2
Species
D. melanogaster
Name
FlyBase ID
FBal0268415
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
pol32L2
Key Links
Allele class
Nature of the Allele
Allele class
Cytology
Description

A 1.6-kb deletion within Pol32.

Imprecise excision of the progenitor insertion, resulting in a deletion that removes almost the entire Pol32 open reading frame.

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

Pol32L2 individuals show DNA repair defects in a P{w[α]} assay: decreased homologous recombination events despite of unchanged incomplete homologous recombination events that terminate via end joining, as compared to controls.

Mutant larvae are extremely sensitive to methyl methanesulfonate, nitrogen mustard and ionising radiation. They are mildly sensitive to hydroxyurea, but are not sensitive to camptothecin.

Mutants show an approximately 70% decrease in full homologous recombination (HR) repair events in assays of excision and repair events of P{hswa}. Analysis of repair synthesis tract lengths suggests that this is due to a defect in primary repair synthesis.

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

PolD3L2 has abnormal DNA repair phenotype, enhanceable by Pif1167

PolD3L2 has abnormal DNA repair phenotype, enhanceable by PolZ13B

NOT Enhanced by
NOT suppressed by
NOT Enhancer of
NOT Suppressor of
Other
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Both Pol32L2, Pif1167 and Pol32L2, DNApol-ζ3B double mutants show more pronounced DNA repair defects in a P{w[α]} assay than Pol32L2 single mutants: more severely decreased homologous recombination events than Pol32L2 and increased incomplete homologous recombination events that terminate via end joining, as compared to wild-type controls.

Pol32L2 mus2053B double mutants show an approximately 70% decrease in full homologous recombination (HR) repair events in assays of excision and repair events of P{hswa} (similar to the reduction seen in Pol32L2 single mutants). Repair synthesis tract lengths are reduced dramatically in aborted HR repair products compared to wild type, and this defect is more severe than that seen in Pol32L2 single mutants.

Pol32L2 DNApol-η12 double mutants show a 60% decrease in full HR repair events in assays of excision and repair events of P{hswa}, but repair synthesis tract lengths of aborted HR products are increased dramatically over wild type.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (4)