<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mizuguchi T</submitter><funding>Howard Hughes Medical Institute</funding><funding>HHS | NIH | National Cancer Institute</funding><pagination>5479-5484</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5448194</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>114(21)</volume><pubmed_abstract>The dynamic nature of genome organization impacts critical nuclear functions including the regulation of gene expression, replication, and DNA damage repair. Despite significant progress, the mechanisms responsible for reorganization of the genome in response to cellular stress, such as aberrant DNA replication, are poorly understood. Here, we show that fission yeast cells carrying a mutation in the DNA-binding protein Sap1 show defects in DNA replication progression and genome stability and display extensive changes in genome organization. Chromosomal regions such as subtelomeres that show defects in replication progression associate with the nuclear envelope in &lt;i>sap1&lt;/i> mutant cells. Moreover, high-resolution, genome-wide chromosome conformation capture (Hi-C) analysis revealed promin</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pubmed_title>Shelterin components mediate genome reorganization in response to replication stress.</pubmed_title><pmcid>PMC5448194</pmcid><funding_grant_id>8341225</funding_grant_id><pubmed_authors>FitzGerald P</pubmed_authors><pubmed_authors>Matsuda E</pubmed_authors><pubmed_authors>Belton JM</pubmed_authors><pubmed_authors>Dekker J</pubmed_authors><pubmed_authors>Taneja N</pubmed_authors><pubmed_authors>Grewal SIS</pubmed_authors><pubmed_authors>Mizuguchi T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Shelterin components mediate genome reorganization in response to replication stress.</name><description>The dynamic nature of genome organization impacts critical nuclear functions including the regulation of gene expression, replication, and DNA damage repair. Despite significant progress, the mechanisms responsible for reorganization of the genome in response to cellular stress, such as aberrant DNA replication, are poorly understood. Here, we show that fission yeast cells carrying a mutation in the DNA-binding protein Sap1 show defects in DNA replication progression and genome stability and display extensive changes in genome organization. Chromosomal regions such as subtelomeres that show defects in replication progression associate with the nuclear envelope in &lt;i>sap1&lt;/i> mutant cells. Moreover, high-resolution, genome-wide chromosome conformation capture (Hi-C) analysis revealed promin</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 May</publication><modification>2026-04-07T18:38:10.328Z</modification><creation>2019-03-27T02:46:13Z</creation></dates><accession>S-EPMC5448194</accession><cross_references><pubmed>28490498</pubmed><doi>10.1073/pnas.1705527114</doi></cross_references></HashMap>