REC, Drosophila MCM8, drives formation of meiotic crossovers.

Crossovers ensure the accurate segregation of homologous chromosomes from one another during meiosis. Here, we describe the identity and function of the Drosophila melanogaster gene recombination defective (rec), which is required for most meiotic crossing over. We show that rec encodes a member of...

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Main Authors: Hunter L Blanton, Sarah J Radford, Susan McMahan, Hutton M Kearney, Joseph G Ibrahim, Jeff Sekelsky
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2005-09-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.0010040&type=printable
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author Hunter L Blanton
Sarah J Radford
Susan McMahan
Hutton M Kearney
Joseph G Ibrahim
Jeff Sekelsky
author_facet Hunter L Blanton
Sarah J Radford
Susan McMahan
Hutton M Kearney
Joseph G Ibrahim
Jeff Sekelsky
author_sort Hunter L Blanton
collection DOAJ
description Crossovers ensure the accurate segregation of homologous chromosomes from one another during meiosis. Here, we describe the identity and function of the Drosophila melanogaster gene recombination defective (rec), which is required for most meiotic crossing over. We show that rec encodes a member of the mini-chromosome maintenance (MCM) protein family. Six MCM proteins (MCM2-7) are essential for DNA replication and are found in all eukaryotes. REC is the Drosophila ortholog of the recently identified seventh member of this family, MCM8. Our phylogenetic analysis reveals the existence of yet another family member, MCM9, and shows that MCM8 and MCM9 arose early in eukaryotic evolution, though one or both have been lost in multiple eukaryotic lineages. Drosophila has lost MCM9 but retained MCM8, represented by REC. We used genetic and molecular methods to study the function of REC in meiotic recombination. Epistasis experiments suggest that REC acts after the Rad51 ortholog SPN-A but before the endonuclease MEI-9. Although crossovers are reduced by 95% in rec mutants, the frequency of noncrossover gene conversion is significantly increased. Interestingly, gene conversion tracts in rec mutants are about half the length of tracts in wild-type flies. To account for these phenotypes, we propose that REC facilitates repair synthesis during meiotic recombination. In the absence of REC, synthesis does not proceed far enough to allow formation of an intermediate that can give rise to crossovers, and recombination proceeds via synthesis-dependent strand annealing to generate only noncrossover products.
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spelling doaj-art-be58af5c2665467fbb28e08d2c9185d32025-08-20T03:22:38ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042005-09-0113e4010.1371/journal.pgen.0010040REC, Drosophila MCM8, drives formation of meiotic crossovers.Hunter L BlantonSarah J RadfordSusan McMahanHutton M KearneyJoseph G IbrahimJeff SekelskyCrossovers ensure the accurate segregation of homologous chromosomes from one another during meiosis. Here, we describe the identity and function of the Drosophila melanogaster gene recombination defective (rec), which is required for most meiotic crossing over. We show that rec encodes a member of the mini-chromosome maintenance (MCM) protein family. Six MCM proteins (MCM2-7) are essential for DNA replication and are found in all eukaryotes. REC is the Drosophila ortholog of the recently identified seventh member of this family, MCM8. Our phylogenetic analysis reveals the existence of yet another family member, MCM9, and shows that MCM8 and MCM9 arose early in eukaryotic evolution, though one or both have been lost in multiple eukaryotic lineages. Drosophila has lost MCM9 but retained MCM8, represented by REC. We used genetic and molecular methods to study the function of REC in meiotic recombination. Epistasis experiments suggest that REC acts after the Rad51 ortholog SPN-A but before the endonuclease MEI-9. Although crossovers are reduced by 95% in rec mutants, the frequency of noncrossover gene conversion is significantly increased. Interestingly, gene conversion tracts in rec mutants are about half the length of tracts in wild-type flies. To account for these phenotypes, we propose that REC facilitates repair synthesis during meiotic recombination. In the absence of REC, synthesis does not proceed far enough to allow formation of an intermediate that can give rise to crossovers, and recombination proceeds via synthesis-dependent strand annealing to generate only noncrossover products.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.0010040&type=printable
spellingShingle Hunter L Blanton
Sarah J Radford
Susan McMahan
Hutton M Kearney
Joseph G Ibrahim
Jeff Sekelsky
REC, Drosophila MCM8, drives formation of meiotic crossovers.
PLoS Genetics
title REC, Drosophila MCM8, drives formation of meiotic crossovers.
title_full REC, Drosophila MCM8, drives formation of meiotic crossovers.
title_fullStr REC, Drosophila MCM8, drives formation of meiotic crossovers.
title_full_unstemmed REC, Drosophila MCM8, drives formation of meiotic crossovers.
title_short REC, Drosophila MCM8, drives formation of meiotic crossovers.
title_sort rec drosophila mcm8 drives formation of meiotic crossovers
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.0010040&type=printable
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