FB2024_03 , released June 25, 2024
Allele: Dmel\Zw104
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General Information
Symbol
Dmel\Zw104
Species
D. melanogaster
Name
FlyBase ID
FBal0012293
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
l(1)zw10i20, zw10i20, zw1065i20
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

An in-frame deletion producing a protein lacking 35 amino acids.

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

Spermatids from mutant third instar larvae testes are multinucleated (with nuclei of variable size) and have a single large nebenkern, indicating defects in chromosome segregation and cytokinesis.

Adult escaper males are sterile, testes are small and contain immotile sperm. Mutant onion stage spermatids vary considerably in size, indicative of chromosome missegregation during both meiotic divisions (nondisjunction during anaphase). Mistakes in chromosome behaviour are visualised by lagging chromosomes and chromatin bridges. Meiotic as well as mitotic defects are specific for events occurring either at anaphase onset or during anaphase proper. Mutation does not cause precocious sister chromatid separation (PSCS) during the first meiotic division but does affect cytokinesis (spermatids containing more than one nucleus per nebenkern).

Embryos derived from homozygous germline clones generally terminate development in the late syncytial blastoderm stages, although 15-25% of develop to later stages of embryogenesis, and 1% hatch into larvae. Mitotic synchrony is lost in embryos derived from homozygous germline clones. Chromatin bridges between nuclei, unequal segregation of chromosomes and lagging chromatids are seen at anaphase.

Brain cells are hyperploid. Aneuploidy involves improper chromosome segregation at anaphase: precocious sister chromatid separation. Mitotic index and the ratio of numbers of cells in anaphase relative to the total number of mitotic figures in larval brains is similar in wild type.

Homozygous germline clone cells are viable but yield inviable eggs.

Males and homozygous females are semi-lethal. Surviving flies have reduced rough eyes, bristles on the thorax and head are sometimes missing, wings are abnormal with a thin texture and thickened veins.

Semilethality is polyphasic, occurs during larval, pupal and adult stages. Mosaic analysis demonstrates mutant phenotype is non-autonomous. Surviving males have rough reduced eyes, wings have thickened veins and incisions on the inner margin. Thoracic hairs are irregularly arranged, dorsocentral, scutellar, ocellar, orbital and vertical bristles are frequently absent. Sperm are immotile.

temperature-sensitive

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments

Lethal phenotype can be rescued by P element mediated transformation of a wild type mit(1)15 gene copy.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Alexander.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (8)