FB2024_03 , released June 25, 2024
Allele: Dmel\Cp110Δ
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General Information
Symbol
Dmel\Cp110Δ
Species
D. melanogaster
Name
FlyBase ID
FBal0294119
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Cytology
Description

FLP mediated recombination between the two progenitor insertions, PBac{RB}Cp110e00667 and P{XP}l(1)G0196d05025 has deleted the Cp110 coding region.

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

Scer\FRT-mediated recombination between the two progenitor insertions has resulted in the deletion of the genomic sequence between them, removing the Cp110 coding sequence.

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

Cp110Δ wing disc centrioles are shorter with prominent extensions of individual microtubules emanating from one end.

Cp110Δ males exhibit a reduction in sperm motility.

Cp110Δ adults exhibit a reduction in climbing ability and abnormal wing posture.

Cp110Δ mutant males display long centriole phenotype in some male germline stem cells in adult testes.

There is no difference in centriole number or number of mitotic defects between Cp110Δ mutant larval brain cells and wild-type.

Cp110Δ syncytial embryos do not exhibit any defects in centrosome behavior, spindle formation, progression through the cell cycle, or chromosome segregation.

Cp110Δ primary spermatocytes exhibit centrioles that are indistinguishable from wild-type. Older spermatocytes develop centrioles that may be slightly elongated and axonemes that are slightly shorter than in wild-type. Approximately 4% of axonemes exhibit one or more missing microtubule doublet. The centrioles in Cp110Δ spermatocytes also display a slight but significant tendency to separate prematurely (often leading to centriole mis-segregation during meiosis).

Cp110Δ mutant larval wing disc centrioles exhibit extensive microtubule protrusions emanating from their distal ends. The protrusions are often many times longer than the centrioles themselves - the longest being >5υm in length, which is approximately 50 times longer than the centriole. These microtubule protrusions are also seen in larval brain cells.

The centrioles in Cp110Δ wing discs are slightly (approximately 10%) but significantly longer than those in wild-type controls.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference
NOT Enhanced by
Statement
Reference
NOT suppressed by
Statement
Reference
NOT Enhancer of
Statement
Reference
NOT Suppressor of
Statement
Reference
Phenotype Manifest In
Enhanced by
Statement
Reference

Cp110Δ has spermatozoon phenotype, enhanceable by Cep97Δ

Cp110Δ has centriole phenotype, enhanceable by Sas-4Ubi.P.GFP

NOT Enhanced by
Statement
Reference

Cp110Δ has centriole phenotype, non-enhanceable by Cep97Δ

NOT suppressed by
Statement
Reference

Cp110Δ has centriole phenotype, non-suppressible by Cep97Δ

NOT Enhancer of
Statement
Reference

Cp110Δ is a non-enhancer of centriole phenotype of Cep97Δ

Cp110Δ is a non-enhancer of spermatozoon phenotype of Cep97Δ

NOT Suppressor of
Statement
Reference

Cp110Δ is a non-suppressor of centriole phenotype of Cep97Δ

Cp110Δ is a non-suppressor of spermatozoon phenotype of Cep97Δ

Cp110Δ is a non-suppressor of primary spermatocyte | P-stage phenotype of Cep97Δ

Additional Comments
Genetic Interactions
Statement
Reference

In a Cp110Δ background, Sas-4Ubi.P.T:Avic\GFP expression leads to an increase in centriole length by approximately 30%.

In a Cp110Δ background, Sas-4Ubi.P.T:Avic\GFP expression leads to an increase in centriole length by approximately 30%.

Co-expression of Sas-6Ubi.P.T:Avic\GFP and ana2Scer\UAS.P\T.T:Avic\GFP does not perturb centriole length in wild-type wing disc cells.

Co-expression of Sas-6Ubi.P.T:Avic\GFP and ana2Scer\UAS.P\T.T:Avic\GFP dramatically increases centriole length (by approximately 60% in Cp110Δ wing disc cells.

Overexpression of ana2Scer\UAS.P\T.T:Avic\GFP increases centriole length (by approximately 60% in Cp110Δ wing disc cells.

Overexpression of Sas-6Ubi.P.T:Avic\GFP increases centriole length (by approximately 60% in Cp110Δ wing disc cells.

Overexpression of Sas-6Ubi.P.T:Avic\GFP in Cp110Δ third instar larval brain cells leads to significant centriole overduplication (with approximately 60% of cells exhibiting overduplication).

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

A Cp110S.Ubi-p63E.T:Avic\GFP-m6 background rescues premature centriole mis-segregation during meiosis in Cp110Δ mutants.

The formation of microtubule protrusions from Cp110Δ centrioles is suppressed by the presence of Cp110S.Ubi-p63E.T:Avic\GFP-m6.

A Cp110L.Ubi-p63E.T:Avic\GFP-m6 background rescues premature centriole mis-segregation during meiosis in Cp110Δ mutants.

The formation of microtubule protrusions from Cp110Δ centrioles is suppressed by the presence of Cp110L.Ubi-p63E.T:Avic\GFP-m6.

Expression of Cp110L.Ubi-p63E.T:Avic\GFP-m6 rescues the long centriole phenotype found in Cp110Δ wing disc cells.

Expression of Cp110L.Ubi-p63E.T:Avic\GFP-m6 weakly rescues the long centriole phenotype found in Cp110Δ wing disc cells.

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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)