FB2024_03 , released June 25, 2024
Allele: Dmel\ovoD1r+
Open Close
General Information
Symbol
Dmel\ovoD1r+
Species
D. melanogaster
Name
FlyBase ID
FBal0090210
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Transgenic product class
Nature of the Allele
Transgenic product class
Progenitor genotype
Carried in construct
Cytology
Description

A 10.5kb genomic ovo fragment derived from ovoD1 flies, with nucleotides 1270 to 1865 replaced with wild-type ovo sequences (this replaces the nucleotide that is mutated in ovoD1 with the wild-type ovo sequence).

Allele components
Component
Use(s)
Regulatory region(s)
Encoded product / tool
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

ovoD3/+ females carrying ovoD1r+ produce embryos, but they die before hatching with gross and variable defects in cuticle differentiation including holes, especially anteriorly, segment deletions and fusions, failed head involution and deletions of anterior elements of the mouthparts.

Females carrying ovoΔa in a wild-type or ovo-/+ background are fertile.

Underexpression of ovo+ in females causes an extreme reduction in germ cell number. Most males bearing an extra 3 to 5 copies of ovo+ exhibit testes with wild type gross morphology and are at least semi-fertile. Nearly all males exhibit some spermatid cysts with defects. The most common defect is cells with a single large mitochondrial derivative surrounded by four spermatid nuclei, this is believed to be due to defects in the completion of cytokinesis during meiosis. Most rarely altered spermatid nuclei sizes are seen. Extra copies of ovo+ do not affect development of the male germline.

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
Rescues
Comments

The maternal effect lethality can be rescued by ovoΔa2, ovoamk or ovoΔap.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
ovoD1r+
Name Synonyms
Secondary FlyBase IDs
    References (6)