FB2024_03 , released June 25, 2024
Allele: Dmel\BubR1D1326N
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General Information
Symbol
Dmel\BubR1D1326N
Species
D. melanogaster
Name
FlyBase ID
FBal0155010
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: D1326N.

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

G5969647A

Reported nucleotide change:

G?A

Amino acid change:

D1326N | BubR1-PA

Reported amino acid change:

D1326N

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

onion stage spermatid & nucleus

Detailed Description
Statement
Reference

The spindle assembly checkpoint is functional in mutant animals; colchicine treatment causes a significant increase in mitotic index in mutant larval neuroblasts but does not significantly increase precocious sister-chromatid separation.

Homozygous and BubR1D1326N/Df(2R)nap9 males show an elevated frequency of nondisjunction of the sex and fourth chromosomes. The majority of nondisjunction in homozygous males is due to precocious sister-chromatid separation, lagging chromosomes and mis-division at anaphase I and metaphase II.

Homozygous females show an elevated frequency of nondisjunction of the sex and fourth chromosomes. The majority of chromosome nondisjunction in homozygous females appears to be the consequence of a failure to separate properly at meiosis II. The total frequency of meiotic exchange of homozygous females is little if at all affected compared to wild type. However, there are subtle, but highly reproducible, effects on the distribution of exchanges. There is a slight increase in the frequency of non-exchange and a corresponding decrease in the frequency of double crossover on the X chromosome. There is a slight increase in the frequency of crossing over between the pericentric markers st and p on the third chromosome, and a corresponding, but equally weak, reduction in the frequency of crossing over in more distal intervals. There is also an increase in the frequency of non-exchange tetrads and a decrease in the frequency of triple crossover tetrads on the autosomes. Homozygous and BubR1D1326N/BubR1Rev1 females show elevated frequencies of exchange in the pericentromeric heterochromatin of the X chromosome.

Homozygous males are fertile, but their progeny show paternal chromosome loss (loss rate of paternal chromosome 4 is 7%). The timing of the chromosome loss appears to be meiotic, based on the observation of micro- and/or macro-nuclei in onion-stage spermatids.

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
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Symbol Synonym
BubR1D1326N
mcl(2)Z1525Z1525
Name Synonyms
Secondary FlyBase IDs
    References (3)