<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pujadas Liwag EM</submitter><funding>NIAID NIH HHS</funding><funding>Northwestern University</funding><funding>Christina Carinato Charitable Foundation</funding><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>jcs262161</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11883274</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>138(3)</volume><pubmed_abstract>Disrupted nuclear shape is associated with multiple pathological processes including premature aging disorders, cancer-relevant chromosomal rearrangements and DNA damage. Nuclear blebs (i.e. herniations of the nuclear envelope) can be induced by (1) nuclear compression, (2) nuclear migration (e.g. cancer metastasis), (3) actin contraction, (4) lamin mutation or depletion, and (5) heterochromatin enzyme inhibition. Recent work has shown that chromatin transformation is a hallmark of bleb formation, but the transformation of higher-order structures in blebs is not well understood. As higher-order chromatin has been shown to assemble into nanoscopic packing domains, we investigated whether (1) packing domain organization is altered within nuclear blebs and (2) whether alteration in packing do</pubmed_abstract><journal>Journal of cell science</journal><pubmed_title>Nuclear blebs are associated with destabilized chromatin-packing domains.</pubmed_title><pmcid>PMC11883274</pmcid><funding_grant_id>EFMA-1830961</funding_grant_id><funding_grant_id>U54CA261694</funding_grant_id><funding_grant_id>T32 AI083216</funding_grant_id><funding_grant_id>R00 GM123195</funding_grant_id><funding_grant_id>R35 GM154928</funding_grant_id><funding_grant_id>UM1 HG011536</funding_grant_id><funding_grant_id>1UM1HG011536</funding_grant_id><funding_grant_id>R01 CA228272</funding_grant_id><funding_grant_id>T32AI083216</funding_grant_id><funding_grant_id>U54 CA268084</funding_grant_id><funding_grant_id>R01CA228272</funding_grant_id><funding_grant_id>R00GM123195</funding_grant_id><funding_grant_id>U54CA268084</funding_grant_id><funding_grant_id>EFMA-1830969</funding_grant_id><funding_grant_id>U54 CA261694</funding_grant_id><pubmed_authors>Pujadas Liwag EM</pubmed_authors><pubmed_authors>Stephens AD</pubmed_authors><pubmed_authors>Su YP</pubmed_authors><pubmed_authors>Almassalha LM</pubmed_authors><pubmed_authors>Gong R</pubmed_authors><pubmed_authors>Acosta N</pubmed_authors><pubmed_authors>Backman V</pubmed_authors><pubmed_authors>Kanemaki MT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nuclear blebs are associated with destabilized chromatin-packing domains.</name><description>Disrupted nuclear shape is associated with multiple pathological processes including premature aging disorders, cancer-relevant chromosomal rearrangements and DNA damage. Nuclear blebs (i.e. herniations of the nuclear envelope) can be induced by (1) nuclear compression, (2) nuclear migration (e.g. cancer metastasis), (3) actin contraction, (4) lamin mutation or depletion, and (5) heterochromatin enzyme inhibition. Recent work has shown that chromatin transformation is a hallmark of bleb formation, but the transformation of higher-order structures in blebs is not well understood. As higher-order chromatin has been shown to assemble into nanoscopic packing domains, we investigated whether (1) packing domain organization is altered within nuclear blebs and (2) whether alteration in packing do</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-05-29T14:31:56.79Z</modification><creation>2025-04-07T11:26:22.198Z</creation></dates><accession>S-EPMC11883274</accession><cross_references><pubmed>39878045</pubmed><doi>10.1242/jcs.262161</doi></cross_references></HashMap>