A Meiotic Mutant Affecting Recombination in Female Drosophila Melanogaster
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mei-S282 is a female meiotic mutant isolated from a natural population of Drosophila melanogaster. It is a recessive mutation located at approximately map position 5 on the third chromosome which has two major effects. It causes a nonuniform decrease in recombination which is most drastic in distal chromosome regions and nondisjunction of all chromosome pairs is elevated at the first meiotic division. Nondisjunctional events are positively correlated; furthermore, nondisjoining chromosomes, themselves nonrecombinant, are preferentially recovered from cells in which nonhomologs are preferentially recovered from cells in which nonhomologs are also non-recombinant.-It is concluded that mei-S282 is a defect which occurs early in meiosis I prior to the time of exchange. In the mutant, the frequency of no-exchange tetrads for each of the major chromosomes is increased-and in cells which contain two or more no-exchange tetrads, an interaction between these chromosomes leads to correlated nondisjunction. mei-S282(+) then, is an exchange precondition necessary for the normal frequency and distribution of exchanges.
Meiotic, genomic and evolutionary properties of crossover distribution in Drosophila yakuba.
Pettie N, Llopart A, Comeron J PLoS Genet. 2022; 18(3):e1010087.
PMID: 35320272 PMC: 8979470. DOI: 10.1371/journal.pgen.1010087.
Female Meiosis: Synapsis, Recombination, and Segregation in .
Hughes S, Miller D, Miller A, Hawley R Genetics. 2018; 208(3):875-908.
PMID: 29487146 PMC: 5844340. DOI: 10.1534/genetics.117.300081.
Miller D, Smith C, Kazemi N, Cockrell A, Arvanitakis A, Blumenstiel J Genetics. 2016; 203(1):159-71.
PMID: 26944917 PMC: 4858771. DOI: 10.1534/genetics.115.186486.
Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.
Middlebrooks C, Mukhopadhyay N, Tinker S, Allen E, Bean L, Begum F Hum Mol Genet. 2013; 23(2):408-17.
PMID: 24014426 PMC: 3869361. DOI: 10.1093/hmg/ddt433.
Page S, McKim K, Deneen B, Van Hook T, Hawley R Genetics. 2000; 155(4):1757-72.
PMID: 10924472 PMC: 1461182. DOI: 10.1093/genetics/155.4.1757.