<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ziesel A</submitter><funding>Intramural research program, Center for Cancer Research, National Cancer Institute</funding><funding>National Institutes of Health General Medicine</funding><funding>Private donation from Eugene and Carol Cheng</funding><funding>NIGMS NIH HHS</funding><pagination>e1010407</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9779700</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(12)</volume><pubmed_abstract>During meiosis, recombination between homologous chromosomes (homologs) generates crossovers that promote proper segregation at the first meiotic division. Recombination is initiated by Spo11-catalyzed DNA double strand breaks (DSBs). 5' end resection of the DSBs creates 3' single strand tails that two recombinases, Rad51 and Dmc1, bind to form presynaptic filaments that search for homology, mediate strand invasion and generate displacement loops (D-loops). D-loop processing then forms crossover and non-crossover recombinants. Meiotic recombination occurs in two temporally distinct phases. During Phase 1, Rad51 is inhibited and Dmc1 mediates the interhomolog recombination that promotes homolog synapsis. In Phase 2, Rad51 becomes active and functions with Rad54 to repair residual DSBs, maki</pubmed_abstract><journal>PLoS genetics</journal><pubmed_title>Rad51-mediated interhomolog recombination during budding yeast meiosis is promoted by the meiotic recombination checkpoint and the conserved Pif1 helicase.</pubmed_title><pmcid>PMC9779700</pmcid><funding_grant_id>GM R01 050717; R35 140684</funding_grant_id><funding_grant_id>GM R01 125800</funding_grant_id><funding_grant_id>R35 GM140684</funding_grant_id><pubmed_authors>Ziesel A</pubmed_authors><pubmed_authors>Weng Q</pubmed_authors><pubmed_authors>Cheng E</pubmed_authors><pubmed_authors>Bhattacharya A</pubmed_authors><pubmed_authors>Dutta R</pubmed_authors><pubmed_authors>Lichten M</pubmed_authors><pubmed_authors>Ahuja JS</pubmed_authors><pubmed_authors>Hollingsworth NM</pubmed_authors><pubmed_authors>Borner GV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rad51-mediated interhomolog recombination during budding yeast meiosis is promoted by the meiotic recombination checkpoint and the conserved Pif1 helicase.</name><description>During meiosis, recombination between homologous chromosomes (homologs) generates crossovers that promote proper segregation at the first meiotic division. Recombination is initiated by Spo11-catalyzed DNA double strand breaks (DSBs). 5' end resection of the DSBs creates 3' single strand tails that two recombinases, Rad51 and Dmc1, bind to form presynaptic filaments that search for homology, mediate strand invasion and generate displacement loops (D-loops). D-loop processing then forms crossover and non-crossover recombinants. Meiotic recombination occurs in two temporally distinct phases. During Phase 1, Rad51 is inhibited and Dmc1 mediates the interhomolog recombination that promotes homolog synapsis. In Phase 2, Rad51 becomes active and functions with Rad54 to repair residual DSBs, maki</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T13:49:08.668Z</modification><creation>2025-04-04T13:49:08.668Z</creation></dates><accession>S-EPMC9779700</accession><cross_references><pubmed>36508468</pubmed><doi>10.1371/journal.pgen.1010407</doi></cross_references></HashMap>