<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Liu X</submitter><pubmed_abstract>The multifunctional protein p100 is a vital transcriptional regulator that increases gene transcription by forming a physical bridge between promoter-specific transcription factors and the basal transcription machinery. To identify potential signal transduction pathways in which human p100 acts as a coregulator and to find target promoter regions that may interact with p100, we performed a promoter microarray assay called chromatin immunoprecipitation-guided ligation and selection (ChIP-GLAS). From this assay, we determined that a set of promoter fragments, including several factors in the transforming growth factor beta (TGF-?) signaling pathway, exhibited interaction with p100. The ChIP-GLAS data were validated by RT-PCR assessing the mRNA expression of various factors in the TGF-? signaling pathway in cell lines.</pubmed_abstract><journal>Cellular &amp; molecular immunology</journal><pagination>88-91</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4002985</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of p100 target promoters by chromatin immunoprecipitation-guided ligation and selection (ChIP-GLAS).</pubmed_title><pmcid>PMC4002985</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Jing X</pubmed_authors><pubmed_authors>Yao Z</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Dong L</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Ge L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of p100 target promoters by chromatin immunoprecipitation-guided ligation and selection (ChIP-GLAS).</name><description>The multifunctional protein p100 is a vital transcriptional regulator that increases gene transcription by forming a physical bridge between promoter-specific transcription factors and the basal transcription machinery. To identify potential signal transduction pathways in which human p100 acts as a coregulator and to find target promoter regions that may interact with p100, we performed a promoter microarray assay called chromatin immunoprecipitation-guided ligation and selection (ChIP-GLAS). From this assay, we determined that a set of promoter fragments, including several factors in the transforming growth factor beta (TGF-?) signaling pathway, exhibited interaction with p100. The ChIP-GLAS data were validated by RT-PCR assessing the mRNA expression of various factors in the TGF-? signaling pathway in cell lines.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jan</publication><modification>2020-11-19T08:16:34Z</modification><creation>2020-11-19T08:16:34Z</creation></dates><accession>S-EPMC4002985</accession><cross_references><pubmed>20921938</pubmed><doi>10.1038/cmi.2010.47</doi></cross_references></HashMap>