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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">6592</item><item key="factors"><item><item key="GSM783825"><item key="CELL TYPE">anterior trunk cells</item><item key="CHIP ANTIBODY">not specified</item></item></item><item><item key="GSM783825"><item key="CELL TYPE">anterior trunk cells</item><item key="CHIP ANTIBODY">not specified</item></item></item><item><item key="GSM783827"><item key="CELL TYPE">forebrain cells</item><item key="CHIP ANTIBODY">not specified</item></item></item><item><item key="GSM783827"><item key="CELL TYPE">forebrain cells</item><item key="CHIP ANTIBODY">not specified</item></item></item><item><item key="GSM783829"><item key="CELL TYPE">posterior trunk cells</item><item key="CHIP ANTIBODY">not specified</item></item></item><item><item key="GSM783829"><item key="CELL TYPE">posterior trunk cells</item><item key="CHIP ANTIBODY">not specified</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">The spatial and temporal control of Hox gene transcription is essential for patterning the vertebrate body axis. Although this process...</item><item key="pubmed_id">21998387</item><item key="geo_gse_id">E-GEOD-31570</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">6</item><item key="tags"><item>axis</item><item>body</item><item>cell</item><item>chromatin</item><item>compartment</item><item>histone</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">the-dynamic-architecture-of-hox-gene-clusters</item><item key="geo_id_plat">E-GEOD-31570_A-AFFY-45</item><item key="name">The Dynamic Architecture of Hox Gene Clusters</item><item key="created">Nov.11, 2014</item><item key="summary">The spatial and temporal control of Hox gene transcription is essential for patterning the vertebrate body axis. Although this process involves changes in histone posttranslational modifications, the existence of particular three-dimensional (3D) architectures remained to be assessed in vivo. Using high-resolution chromatin conformation capture methodology, we examined the spatial configuration of Hox clusters in embryonic mouse tissues where different Hox genes are active. When the cluster is transcriptionally inactive, Hox genes associate into a single 3D structure delimited from flanking regions. Once transcription starts, Hox clusters switch to a bimodal 3D organization where newly activated genes progressively cluster into a transcriptionally active compartment. This transition in spatial configurations coincides with the dynamics of chromatin marks, which label the progression of the gene clusters from a negative to a positive transcription status. This spatial compartmentalization may be key to process the collinear activation of these compact gene clusters. Examination of gene expression in 3 cell types. Examination of 2 different histone modifications in 2 cell types.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-31570</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-31570/samples/</item></data></biogps>
