FB2025_01 , released February 20, 2025
Allele: Dmel\mars91
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General Information
Symbol
Dmel\mars91
Species
D. melanogaster
Name
FlyBase ID
FBal0246631
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Imprecise excision of the progenitor insertion results in a deletion which removes 531 bp of the first exon of mars, including the start codon.

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

531bp deletion resulting from imprecise excision of P{EP}drkEP2477

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

When treated with a low concentration of demecolcine, which partially depolymerises microtubles from mitotic spindles, approximately 50% of mars91 mutant embryos completely lose microtubules from around the chromosomes, while the remaining embryos exhibit much weaker staining of the microtubules. mars91 mutants are less resistant to demecolcine microtubule depolymerisation.

mars91 embryonic cells exhibit dissociation of centrosomes from mitotic spindles. The mitotic spindles without centrosomes tend to collapse into monopolar spindles.

90.8% of embryos from homozygous mars91 parents die during embryogenesis, with the majority of embryos displaying defects in cellularisation. 9.2% hatch into larvae, but only 5.5% of embryos survive to adulthood. Embryos from mars91 homozygous parents display severe mitotic defects during the rapid nuclear divisions in early syncytial blastoderm stage embryos. Centrosomes frequently detach from spindles and from the nuclear envelope and nucleate astral microtubules in ectopic positions.

mars91/Df(2R)CX1 animals are viable and fertile. Offspring of mars91/Df(2R)CX1 have severe embryonic defects and the majority die during embryogenesis.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of mars1-430.Scer\UAS.P\T.N.T:Avic\GFP fails to rescue the lethality associated with mars91 mutants but is able to largely maintain the mitotic spindle morphology in the absence of endogenous mars.

Expression of marsScer\UAS.P\T.T:Avic\GFP-EGFP under the control of Scer\GAL4mat.αTub67C.T:Hsim\VP16 fully rescues the embryogenesis defects in offspring from mars91 homozygous parents.

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Mutant
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Stocks (0)
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External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
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Name Synonyms
Secondary FlyBase IDs
    References (2)