<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/GSE295nnn/GSE295340/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</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=GSE295340</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Polycomb Chromatin Topology Enables Long-Range Enhancer Recruitment during Craniofacial Development [ChIP-seq]</name><description>Little is known about how three-dimensional chromatin topology shapes mammalian craniofacial development. In mouse cranial neural crest cells, a Polycomb Repressive Complex 2 (PRC2)-dependent chromatin architecture is established before migration. This configuration maintains craniofacial gene promoters poised and connects them with distal Polycomb tethering elements, positioning promoters in spatial proximity to future long-range enhancers. Deletion of Ezh2 disrupts this early topology, causing inappropriate gene derepression in post-migratory craniofacial subpopulations where these genes are normally silenced, and failure of long-range enhancer recruitment where activation is required, thereby impairing proper gene expression. We further identify a distal Polycomb tethering element essential for Hoxa2 enhancer recruitment across topologically associating domains. Thus, Polycomb acts not only as a transcriptional repressor, but also as a chromatin-folding organizer that prepares developmental genes for later activation, by facilitating subsequent recruitment of distal active enhancers previously not in contact. Polycomb-mediated topology therefore orchestrates the transition from progenitor plasticity to precise spatiotemporal control of morphogenetic gene programs during neural crest development and face formation.</description><dates><publication>2026/04/08</publication></dates><accession>GSE295340</accession><cross_references><GSM>GSM8945979</GSM><GSM>GSM8945978</GSM><GSM>GSM8945977</GSM><GSM>GSM8945976</GSM><GSM>GSM8945975</GSM><GSM>GSM8945974</GSM><GSM>GSM8945973</GSM><GSM>GSM8945972</GSM><GSM>GSM8945971</GSM><GSM>GSM8945970</GSM><GSM>GSM8945991</GSM><GSM>GSM8945990</GSM><GSM>GSM9562060</GSM><GSM>GSM9562061</GSM><GSM>GSM8945969</GSM><GSM>GSM8945968</GSM><GSM>GSM8945989</GSM><GSM>GSM8945967</GSM><GSM>GSM8945988</GSM><GSM>GSM8945966</GSM><GSM>GSM8945965</GSM><GSM>GSM8945987</GSM><GSM>GSM8945986</GSM><GSM>GSM8945964</GSM><GSM>GSM8945985</GSM><GSM>GSM8945963</GSM><GSM>GSM8945962</GSM><GSM>GSM8945984</GSM><GSM>GSM8945983</GSM><GSM>GSM8945982</GSM><GSM>GSM8945981</GSM><GSM>GSM8945980</GSM><GSM>GSM9562057</GSM><GSM>GSM9562056</GSM><GSM>GSM9562059</GSM><GSM>GSM9562058</GSM><GSM>GSM9562053</GSM><GSM>GSM9562052</GSM><GSM>GSM9562055</GSM><GSM>GSM9562054</GSM><GSM>GSM9562051</GSM><GSM>GSM9562050</GSM><GPL>17021</GPL><GPL>24247</GPL><GSE>295340</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>