FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\mod(mdg4)Z3-5578
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General Information
Symbol
Dmel\mod(mdg4)Z3-5578
Species
D. melanogaster
Name
FlyBase ID
FBal0194707
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
mnmZ3-5578
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description

The stop mutation is in the C-terminal coding exon, which is present in most mod(mdg4) isoforms.

Amino acid replacement: W449term.

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

mod(mdg4)Z3-3298/mod(mdg4)Z3-5578 males exhibit defects in chromosome segregation (i.e. random segregation of sex chromosomes) and conjunction during meiosis I; abnormal chromosome territories during S5, S6 and prometaphase I stages; an increased number of smaller DNA blobs (chromosome masses) during prometaphase I; prematurely separated bivalents into univalents during meiosis I; and a striking size variation among the nuclei present in spermatid cysts compared to controls.

mod(mdg4)Z3-5578 spermatocytes show precocious separation of homologs and reduced chromosome condensation.

Homozygous males show a high frequency of X-Y chromosome nondisjunction in meiosis (51.2%).

mod(mdg4)Z3-5578/Df(3R)GC14 males show a high frequency of 4th chromosome loss (28.1%) and chromosome 2 nondisjunction (43.3%) in meiosis.

mod(mdg4)Z3-5578/Df(3R)GC14 females do not show increased X chromosome nondisjunction compared to controls and the frequency of recombination in large intervals on the X and third chromosomes in the mutant females is normal.

mod(mdg4)Z3-5578 mutants show elevated frequencies of autosomal and sex chromosome nondisjunction. Analysis of mutant spermatocytes shows that nondisjunction is limited largely to meiosis I. Premeiotic and meiotic homolog pairing are normal. The earliest observable phenotype is that of "territory expansion" in late G2, with homologous chromosomes being at a greater distance from one another than in wild-type spermatocytes. mod(mdg4)Z3-5578 spermatocytes show incomplete chromatin condensation and form up to eight large clumps of chromatin form by metaphase I, instead of the one central mass observed in wild type. The clumps represent bivalents and univalents, consistent with a defect in formation or maintenance of bivalents. In early anaphase I, chromosomes are distributed unevenly and asymmetrically along the spindle. In late anaphase I, there is a high frequency of laggards and polar chromatin masses of unequal size, indicating high frequency of nondisjunction.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
NOT Enhancer of
NOT Suppressor of
Statement
Reference
Other
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

In Toporsf05115/+; mod(mdg4)Z3-5578 males, individual lagging chromosome are observed but no anaphase I bridges are seen. In both Toporsf05115; mod(mdg4)Z3-5578/+ and Toporsf05115; mod(mdg4)Z3-5578 males, nearly all anaphase/telophase figures have a bridge.

The near sterility and nondisjunction phenotypes associated with Toporsf05115 are not improved in a mod(mdg4)Z3-5578 hetero- or homozygous background.

mod(mdg4)Z3-5578, Toporsf05115 double mutants show a meiotic chromsome condensation defect that is more severe than either single mutant.

Body colour: the y2 phenotype (black bristles, yellow body and wings) is not altered by mod(mdg4)Z3-5578/mod(mdg4)T16.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

mod(mdg4)Z3-5578 fully complements the lethal/semi-lethal phenotypes of the following mod(mdg4) alleles, but they fail to complement mod(mdg4)Z3-5578 with respect to X-Y chromosome nondisjunction in male meiosis, with the transheterozygotes showing a high level of X-Y nondisjunction (frequency is indicated in parentheses after each allele); mod(mdg4)T16 (44.3%), mod(mdg4)142Δ10 (46%), mod(mdg4)142Δ33 (37.3%), mod(mdg4)eGp4 (50.3%) and mod(mdg4)B2 (37.3%).

mod(mdg4)Z3-5578 fully complements the lethal/semi-lethal phenotypes of the following mod(mdg4) alleles, and they partially or fully complement mod(mdg4)Z3-5578 with respect to X-Y chromosome nondisjunction in male meiosis, with the transheterozygotes showing only a low level of X-Y nondisjunction (frequency is indicated in parentheses after each allele); mod(mdg4)142Δ15 (0.56%), mod(mdg4)142Δ32 (0.95%), mod(mdg4)142Δ29 (1.54%), mod(mdg4)142Δ49 (0%), mod(mdg4)neo129 (4.46%), mod(mdg4)02 (1.72%), mod(mdg4)03 (0.07%), mod(mdg4)20 (2.96%), mod(mdg4)117 (0.75%), mod(mdg4)269 (1.44%), mod(mdg4)324 (2.84%) and mod(mdg4)340 (1.89%).

mod(mdg4)Z3-3401 strongly (but not completely) complements mod(mdg4)Z3-5578; transheterozygotes show only a low level (1.42%) of X-Y nondisjunction in male meiosis.

mod(mdg4)T6 fully complements mod(mdg4)Z3-5578 with respect to X-Y chromosome nondisjunction in male meiosis.

mod(mdg4)Z3-5578 fails to complement mod(mdg4)Z3-3298 with respect to X-Y chromosome nondisjunction in male meiosis; transheterozygotes show 45.2% X-Y nondisjunction.

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Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)