<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kanno SI</submitter><funding>Naito Foundation</funding><funding>Princess Takamatsu Cancer Research Fund</funding><funding>Takeda Science Foundation</funding><funding>Japan Proteomics Co., Ltd</funding><pagination>gkaf150</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11904782</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53(5)</volume><pubmed_abstract>The SWI/SNF chromatin-remodeling complex that comprises multiple subunits orchestrates diverse cellular processes, including gene expression, DNA repair, and DNA replication, by sliding and releasing nucleosomes. AT-interacting domain-rich protein 1A (ARID1A) and ARID1B (ARID1A/B), a pivotal subunit, have significant relevance in cancer management because they are frequently mutated in a broad range of cancer types. To delineate the protein network involving ARID1A/B, we investigated the interactions of this with other proteins under physiological conditions. The ARID domain of ARID1A/B interacts with proteins involved in transcription and DNA/RNA metabolism. Several proteins are responsible for genome integrity maintenance, including DNA-dependent protein kinase catalytic subunit (DNA-PKc</pubmed_abstract><journal>Nucleic acids research</journal><pubmed_title>Armadillo domain of ARID1A directly interacts with DNA-PKcs to couple chromatin remodeling with nonhomologous end joining (NHEJ) pathway.</pubmed_title><pmcid>PMC11904782</pmcid><funding_grant_id>15-24705</funding_grant_id><pubmed_authors>Kanno SI</pubmed_authors><pubmed_authors>Kobayashi T</pubmed_authors><pubmed_authors>Kurimasa A</pubmed_authors><pubmed_authors>Yasui A</pubmed_authors><pubmed_authors>Tanaka K</pubmed_authors><pubmed_authors>Watanabe R</pubmed_authors><pubmed_authors>Ui A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Armadillo domain of ARID1A directly interacts with DNA-PKcs to couple chromatin remodeling with nonhomologous end joining (NHEJ) pathway.</name><description>The SWI/SNF chromatin-remodeling complex that comprises multiple subunits orchestrates diverse cellular processes, including gene expression, DNA repair, and DNA replication, by sliding and releasing nucleosomes. AT-interacting domain-rich protein 1A (ARID1A) and ARID1B (ARID1A/B), a pivotal subunit, have significant relevance in cancer management because they are frequently mutated in a broad range of cancer types. To delineate the protein network involving ARID1A/B, we investigated the interactions of this with other proteins under physiological conditions. The ARID domain of ARID1A/B interacts with proteins involved in transcription and DNA/RNA metabolism. Several proteins are responsible for genome integrity maintenance, including DNA-dependent protein kinase catalytic subunit (DNA-PKc</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-04-23T03:12:37.867Z</modification><creation>2025-04-04T00:32:11.08Z</creation></dates><accession>S-EPMC11904782</accession><cross_references><pubmed>40087883</pubmed><doi>10.1093/nar/gkaf150</doi></cross_references></HashMap>