<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hernandez-Vicens R</submitter><funding>Ariel University</funding><funding>Ariel Scientific Innovations</funding><funding>Israel Cancer Association</funding><pagination>e13348</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9715361</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>55(12)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>SETDB1 is a methyltransferase responsible for the methylation of histone H3-lysine-9, which is mainly related to heterochromatin formation. SETDB1 is overexpressed in various cancer types and is associated with an aggressive phenotype. In agreement with its activity, it mainly exhibits a nuclear localization; however, in several cell types a cytoplasmic localization was reported. Here we looked for cytoplasmic functions of SETDB1.&lt;h4>Methods&lt;/h4>SETDB1 association with microtubules was detected by immunofluorescence and co-sedimentation. Microtubule dynamics were analysed during recovery from nocodazole treatment and by tracking microtubule plus-ends in live cells. Live cell imaging was used to study mitotic kinetics and protein-protein interaction was identified by co-i</pubmed_abstract><journal>Cell proliferation</journal><pubmed_title>SETDB1 regulates microtubule dynamics.</pubmed_title><pmcid>PMC9715361</pmcid><funding_grant_id>202220036</funding_grant_id><pubmed_authors>Pernicone N</pubmed_authors><pubmed_authors>Listovsky T</pubmed_authors><pubmed_authors>Singh J</pubmed_authors><pubmed_authors>Hernandez-Vicens R</pubmed_authors><pubmed_authors>Gerlitz G</pubmed_authors></additional><is_claimable>false</is_claimable><name>SETDB1 regulates microtubule dynamics.</name><description>&lt;h4>Objectives&lt;/h4>SETDB1 is a methyltransferase responsible for the methylation of histone H3-lysine-9, which is mainly related to heterochromatin formation. SETDB1 is overexpressed in various cancer types and is associated with an aggressive phenotype. In agreement with its activity, it mainly exhibits a nuclear localization; however, in several cell types a cytoplasmic localization was reported. Here we looked for cytoplasmic functions of SETDB1.&lt;h4>Methods&lt;/h4>SETDB1 association with microtubules was detected by immunofluorescence and co-sedimentation. Microtubule dynamics were analysed during recovery from nocodazole treatment and by tracking microtubule plus-ends in live cells. Live cell imaging was used to study mitotic kinetics and protein-protein interaction was identified by co-i</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-05T18:11:27.308Z</modification><creation>2026-04-07T21:46:55.263Z</creation></dates><accession>S-EPMC9715361</accession><cross_references><pubmed>36330589</pubmed><doi>10.1111/cpr.13348</doi></cross_references></HashMap>