<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu T</submitter><funding>NICHD NIH HHS</funding><funding>National Institutes of Health</funding><pagination>100142</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8461376</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20</volume><pubmed_abstract>Chromatin-associated RNAs have diverse roles in the nucleus. However, their mechanisms of action are poorly understood, in part because of the inability to identify proteins that specifically associate with chromatin-bound RNAs. Here, we address this problem for a subset of chromatin-associated RNAs that form R-loops-RNA-DNA hybrid structures that include a displaced strand of ssDNA. R-loops generally form cotranscriptionally and have important roles in regulation of gene expression, immunoglobulin class switching, and other processes. However, unresolved R-loops can lead to DNA damage and chromosome instability. To identify factors that may bind and regulate R-loop accumulation or mediate R-loop-dependent functions, we used a comparative immunoprecipitation/MS approach, with and without R</pubmed_abstract><journal>Molecular &amp; cellular proteomics : MCP</journal><pubmed_title>Characterization of R-Loop-Interacting Proteins in Embryonic Stem Cells Reveals Roles in rRNA Processing and Gene Expression.</pubmed_title><pmcid>PMC8461376</pmcid><funding_grant_id>R01 HD093783</funding_grant_id><funding_grant_id>R01HD072122</funding_grant_id><funding_grant_id>R01 HD072122</funding_grant_id><funding_grant_id>R01HD093783</funding_grant_id><pubmed_authors>Chu F</pubmed_authors><pubmed_authors>Fazzio TG</pubmed_authors><pubmed_authors>Wu T</pubmed_authors><pubmed_authors>Nance J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of R-Loop-Interacting Proteins in Embryonic Stem Cells Reveals Roles in rRNA Processing and Gene Expression.</name><description>Chromatin-associated RNAs have diverse roles in the nucleus. However, their mechanisms of action are poorly understood, in part because of the inability to identify proteins that specifically associate with chromatin-bound RNAs. Here, we address this problem for a subset of chromatin-associated RNAs that form R-loops-RNA-DNA hybrid structures that include a displaced strand of ssDNA. R-loops generally form cotranscriptionally and have important roles in regulation of gene expression, immunoglobulin class switching, and other processes. However, unresolved R-loops can lead to DNA damage and chromosome instability. To identify factors that may bind and regulate R-loop accumulation or mediate R-loop-dependent functions, we used a comparative immunoprecipitation/MS approach, with and without R</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T13:10:43.25Z</modification><creation>2022-02-11T11:29:32.643Z</creation></dates><accession>S-EPMC8461376</accession><cross_references><pubmed>34478875</pubmed><doi>10.1016/j.mcpro.2021.100142</doi></cross_references></HashMap>