<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ganez-Zapater A</submitter><funding>cancerfonden</funding><funding>European Research Council</funding><funding>carl tryggers stiftelse för vetenskaplig forskning</funding><funding>vetenskapsrådet</funding><funding>stockholms universitet</funding><funding>Stockholm University</funding><pagination>463-484</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8960663</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>297(2)</volume><pubmed_abstract>BRG1 and BRM are ATPase core subunits of the human SWI/SNF chromatin remodelling complexes mainly associated with transcriptional initiation. They also have a role in alternative splicing, which has been shown for BRM-containing SWI/SNF complexes at a few genes. Here, we have identified a subset of genes which harbour alternative exons that are affected by SWI/SNF ATPases by expressing the ATPases BRG1 and BRM in C33A cells, a BRG1- and BRM-deficient cell line, and analysed the effect on splicing by RNA sequencing. BRG1- and BRM-affected sub-sets of genes favouring both exon inclusion and exon skipping, with only a minor overlap between the ATPase. Some of the changes in alternative splicing induced by BRG1 and BRM expression did not require the ATPase activity. The BRG1-ATPase independent</pubmed_abstract><journal>Molecular genetics and genomics : MGG</journal><pubmed_title>The SWI/SNF subunit BRG1 affects alternative splicing by changing RNA binding factor interactions with nascent RNA.</pubmed_title><pmcid>PMC8960663</pmcid><funding_grant_id>CAN 2016/460</funding_grant_id><funding_grant_id>2015–04553</funding_grant_id><funding_grant_id>2015-04553</funding_grant_id><funding_grant_id>CTS15:568</funding_grant_id><funding_grant_id>758397</funding_grant_id><pubmed_authors>Visa N</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Ganez-Zapater A</pubmed_authors><pubmed_authors>Mackowiak SD</pubmed_authors><pubmed_authors>Tarbier M</pubmed_authors><pubmed_authors>Ostlund Farrants AK</pubmed_authors><pubmed_authors>Jordan-Pla A</pubmed_authors><pubmed_authors>Friedlander MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The SWI/SNF subunit BRG1 affects alternative splicing by changing RNA binding factor interactions with nascent RNA.</name><description>BRG1 and BRM are ATPase core subunits of the human SWI/SNF chromatin remodelling complexes mainly associated with transcriptional initiation. They also have a role in alternative splicing, which has been shown for BRM-containing SWI/SNF complexes at a few genes. Here, we have identified a subset of genes which harbour alternative exons that are affected by SWI/SNF ATPases by expressing the ATPases BRG1 and BRM in C33A cells, a BRG1- and BRM-deficient cell line, and analysed the effect on splicing by RNA sequencing. BRG1- and BRM-affected sub-sets of genes favouring both exon inclusion and exon skipping, with only a minor overlap between the ATPase. Some of the changes in alternative splicing induced by BRG1 and BRM expression did not require the ATPase activity. The BRG1-ATPase independent</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-05-31T21:03:29.623Z</modification><creation>2025-04-04T21:43:41.862Z</creation></dates><accession>S-EPMC8960663</accession><cross_references><pubmed>35187582</pubmed><doi>10.1007/s00438-022-01863-9</doi></cross_references></HashMap>