FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\mei-S511
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General Information
Symbol
Dmel\mei-S511
Species
D. melanogaster
Name
FlyBase ID
FBal0012189
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
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Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
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Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
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Disease
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Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
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Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

mei-S511 disrupts a number of aspects of chromosome pairing and alignment prior to metaphase and therefore both reduces exchanges and prevents proper partner choice within the distributive system.

Non-disjunction of the X, 2nd, 3rd and 4th chromosomes is increased compared to wild-type in females. There is a positive correlation in the probability of nondisjunction of nonhomologous chromosomes, nondisjoining nonhomologs tend to separate from each other and nondisjunction occurs at the first meiotic division. Crossing over on the X chromosome is uniformly reduced (with the possible exception of the most proximal region which shows a lesser effect) in homozygous females to about 1/2 the control value. Segregation of the sex and 4th chromosomes is normal in mutant males.

Females homozygous for mei-S511 exhibit reduced exchange and high frequencies of nonhomologous disjunction, particularly with respect to the X and fourth chromosomes (XX <-> 44 segregations are frequent). In addition mei-S511 decreases the frequency of secondary nondisjunction in structurally normal XXY females and increases the frequency of nondisjunction in X inversion heterozygotes.

External Data
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Xenogenetic Interactions
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Complementation and Rescue Data
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Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Isolated from: winery, about 15 kilometres northeast of Rome, Italy, October 1965. The main recessive effect of the mei-S511 mutation appears to be synthetic - requiring recessive factors on both chromosomes 2 and 3. The disjunctional anomaly is genetically separable from the crossover effect.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
mei-S511
Name Synonyms
Secondary FlyBase IDs
    References (2)