<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Laha S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Metaphase cells have short spindles for efficient bi-orientation of chromosomes. The cohesin proteins hold sister chromatids together, creating Sister Chromatid Cohesion (SCC) that helps in the maintenance of short spindle lengths in metaphase. The budding yeast protein Chl1p, which has human homologs, is required for DNA damage repair, recombination, transcriptional silencing and aging. This protein is also needed to establish SCC between sister chromatids in S-phase.&lt;h4>Results&lt;/h4>In the present study we have further characterized Chl1p for its role in the yeast Saccharomyces cerevisiae when cells are under replication stress. We show that when DNA replication is arrested by hydroxyurea (HU), the chl1 mutation causes growth deficiency and a mild loss in cell viability</pubmed_abstract><journal>BMC genetics</journal><pagination>83</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3190345</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Functional characterization of the Saccharomyces cerevisiae protein Chl1 reveals the role of sister chromatid cohesion in the maintenance of spindle length during S-phase arrest.</pubmed_title><pmcid>PMC3190345</pmcid><pubmed_authors>Sinha P</pubmed_authors><pubmed_authors>Das SP</pubmed_authors><pubmed_authors>Hajra S</pubmed_authors><pubmed_authors>Laha S</pubmed_authors><pubmed_authors>Sanyal K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional characterization of the Saccharomyces cerevisiae protein Chl1 reveals the role of sister chromatid cohesion in the maintenance of spindle length during S-phase arrest.</name><description>&lt;h4>Background&lt;/h4>Metaphase cells have short spindles for efficient bi-orientation of chromosomes. The cohesin proteins hold sister chromatids together, creating Sister Chromatid Cohesion (SCC) that helps in the maintenance of short spindle lengths in metaphase. The budding yeast protein Chl1p, which has human homologs, is required for DNA damage repair, recombination, transcriptional silencing and aging. This protein is also needed to establish SCC between sister chromatids in S-phase.&lt;h4>Results&lt;/h4>In the present study we have further characterized Chl1p for its role in the yeast Saccharomyces cerevisiae when cells are under replication stress. We show that when DNA replication is arrested by hydroxyurea (HU), the chl1 mutation causes growth deficiency and a mild loss in cell viability</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Sep</publication><modification>2025-04-03T23:07:07.489Z</modification><creation>2019-03-27T00:44:47Z</creation></dates><accession>S-EPMC3190345</accession><cross_references><pubmed>21943249</pubmed><doi>10.1186/1471-2156-12-83</doi></cross_references></HashMap>