<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nadarajan S</submitter><funding>HHS | NIH | National Institute of General Medical Sciences</funding><pagination>e2016363118</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8092412</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>118(17)</volume><pubmed_abstract>The position of recombination events established along chromosomes in early prophase I and the chromosome remodeling that takes place in late prophase I are intrinsically linked steps of meiosis that need to be tightly regulated to ensure accurate chromosome segregation and haploid gamete formation. Here, we show that RAD-51 foci, which form at the sites of programmed meiotic DNA double-strand breaks (DSBs), exhibit a biased distribution toward off-centered positions along the chromosomes in wild-type Caenorhabditis elegans, and we identify two meiotic roles for chromatin-associated protein HIM-17 that ensure normal chromosome remodeling in late prophase I. During early prophase I, HIM-17 regulates the distribution of DSB-dependent RAD-51 foci and crossovers on chromosomes, which is critic</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pubmed_title>HIM-17 regulates the position of recombination events and GSP-1/2 localization to establish short arm identity on bivalents in meiosis.</pubmed_title><pmcid>PMC8092412</pmcid><funding_grant_id>R01GM072551</funding_grant_id><pubmed_authors>Nadarajan S</pubmed_authors><pubmed_authors>Altendorfer E</pubmed_authors><pubmed_authors>Saito TT</pubmed_authors><pubmed_authors>Colaiacovo MP</pubmed_authors><pubmed_authors>Martinez-Garcia M</pubmed_authors></additional><is_claimable>false</is_claimable><name>HIM-17 regulates the position of recombination events and GSP-1/2 localization to establish short arm identity on bivalents in meiosis.</name><description>The position of recombination events established along chromosomes in early prophase I and the chromosome remodeling that takes place in late prophase I are intrinsically linked steps of meiosis that need to be tightly regulated to ensure accurate chromosome segregation and haploid gamete formation. Here, we show that RAD-51 foci, which form at the sites of programmed meiotic DNA double-strand breaks (DSBs), exhibit a biased distribution toward off-centered positions along the chromosomes in wild-type Caenorhabditis elegans, and we identify two meiotic roles for chromatin-associated protein HIM-17 that ensure normal chromosome remodeling in late prophase I. During early prophase I, HIM-17 regulates the distribution of DSB-dependent RAD-51 foci and crossovers on chromosomes, which is critic</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-26T23:38:46.61Z</modification><creation>2025-04-06T17:38:46.236Z</creation></dates><accession>S-EPMC8092412</accession><cross_references><pubmed>33883277</pubmed><doi>10.1073/pnas.2016363118</doi></cross_references></HashMap>