<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE346nnn/GSE346274/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Rattus norvegicus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE346274</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>BRD4 maintains chromaffin-cell identity and promotes pheochromocytoma progression through a SMAD2-dependent transcriptional program</name><description>To determine whether BRD4 directly regulates chromaffin-cell identity genes at the chromatin level, we performed CUT&amp;Tag (Cleavage Under Targets and Tagmentation) using a BRD4-specific antibody in PC12 cells, in parallel with chromatin immunoprecipitation (ChIP). This approach allowed genome-wide mapping of BRD4 occupancy. Our CUT&amp;Tag and ChIP analyses revealed that BRD4 directly occupies the regulatory regions of key chromaffin-cell genes, including TH, CHGB, and PHOX2A. These findings demonstrate that BRD4 acts as a direct transcriptional regulator of genes essential for chromaffin-cell identity and catecholamine biosynthesis, providing a mechanistic basis for its role in maintaining chromaffin-cell function and pheochromocytoma progression.</description><dates><publication>2026/09/10</publication></dates><accession>GSE346274</accession><cross_references><GSM>GSM10031550</GSM><GSM>GSM10031549</GSM><GPL>37481</GPL><GSE>346274</GSE><taxon>Rattus norvegicus</taxon></cross_references></HashMap>