The stop mutation is in the C-terminal coding exon, which is present in most mod(mdg4) isoforms.
Amino acid replacement: W449term.
G2 phase & nuclear chromosome
meiosis I & nuclear chromosome
testis | adult stage (with mod(mdg4)Z3-3298)
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.
mod(mdg4)Z3-5578/mod(mdg4)[+] is a non-enhancer of abnormal meiotic cell cycle | male limited phenotype of Toporsf05115
mod(mdg4)Z3-5578/mod(mdg4)[+] is a non-enhancer of male semi-sterile phenotype of Toporsf05115
mod(mdg4)Z3-5578 is a non-enhancer of abnormal meiotic cell cycle | male limited phenotype of Toporsf05115
mod(mdg4)Z3-5578 is a non-enhancer of male semi-sterile phenotype of Toporsf05115
mod(mdg4)Z3-5578/mod(mdg4)T16 is a non-enhancer of abnormal body color phenotype of y2
mod(mdg4)Z3-5578/mod(mdg4)T16 is a non-suppressor of abnormal body color phenotype of y2
Toporsf05115, mod(mdg4)Z3-5578 has abnormal meiotic cell cycle phenotype
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.
mod(mdg4)Z3-5578/mod(mdg4)Z3-3298 is rescued by mod(mdg4)UAS.mnm/Scer\GAL4VP16.bam
mod(mdg4)Z3-5578 is rescued by mod(mdg4)MNM.hs.EGFP
mod(mdg4)Z3-5578/mod(mdg4)Z3-3298 is partially rescued by mod(mdg4)βTub85D.mnm.C.EGFP
mod(mdg4)Z3-5578/mod(mdg4)Z3-3298 is partially rescued by mod(mdg4)UAS.mnm.N.EGFP/Scer\GAL4VP16.bam
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.