FB2024_03 , released June 25, 2024
Allele: Dmel\mei-9b
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General Information
Symbol
Dmel\mei-9b
Species
D. melanogaster
Name
FlyBase ID
FBal0012172
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: C502T.

Amino acid replacement: Q125term.

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

C4317421T

Reported nucleotide change:

C502T

Amino acid change:

Q169term | mei-9-PA; Q169term | mei-9-PB

Reported amino acid change:

Q125term

Comment:

Position of mutation on reference sequence inferred by FlyBase curator. Authors protein sequence lacks 43 N-terminal amino acid residues.

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

mitosis & nuclear chromosome

Detailed Description
Statement
Reference

mei-9b/mei-9A2 females show 31% X chromosome nondisjunction, compared to 0.33% in wild-type females. mei-9b/mei-9A2 larvae are hypersensitive to ultraviolet light and nitrogen mustard.

Recombination in females is reduced to 16% of control levels. Chiasma frequency greatly reduced. Stage 14 oocytes can finish both meiotic divisions without metaphase arrest. Rare normal metaphase figures indicate that even one chiasma is sufficient to ensure metaphase arrest.

Increases the frequency of X chromosome non-disjunctions in noda mutants.

Homozygotes have an increased frequency of X chromosome non-disjunction.

Reduces meiotic exchange uniformly throughout the euchromatin. Deleted chromatids are occasionally recovered.

Meiotic crossing-over is reduced by a factor of 1/6 in homozygous females. Meiotic crossing-over is reduced by a factor of 1/12 in mei-9a/mei-9b females. The frequency of gene conversion at the ry locus is unaffected in homozygous or mei-9a/mei-9b females. Post-meiotic segregation events, manifested as mosaic progeny, are produced at high frequency in homozygous and mei-9a/mei-9b females.

Homozygotes and hemizygotes show a higher frequency of spontaneous chromosome aberrations in neuroblast metaphases than wild-type larvae. The ratio of chromatid breaks to isochromatid breaks is 5.9-8.6. Approximately half of the breaks are heterochromatic and half are euchromatic. The breaks appear to be randomly distributed among the chromosomes. Breaks are 1.4-1.6 times more frequent in females than in males.

mutagen sensitive reduces exchange mitotic instability

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

Simple meiotic gene conversion tracts produced in mei-9 mutants have been compared with those produced in wild-type.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (12)