<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ronzio M</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><pagination>e1008488</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7793273</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(12)</volume><pubmed_abstract>NF-Y is a trimeric Transcription Factor -TF- which binds with high selectivity to the conserved CCAAT element. Individual ChIP-seq analysis as well as ENCODE have progressively identified locations shared by other TFs. Here, we have analyzed data introduced by ENCODE over the last five years in K562, HeLa-S3 and GM12878, including several chromatin features, as well RNA-seq profiling of HeLa cells after NF-Y inactivation. We double the number of sequence-specific TFs and co-factors reported. We catalogue them in 4 classes based on co-association criteria, infer target genes categorizations, identify positional bias of binding sites and gene expression changes. Larger and novel co-associations emerge, specifically concerning subunits of repressive complexes as well as RNA-binding proteins. On the one hand, these data better define NF-Y association with single members of major classes of TFs, on the other, they suggest that it might have a wider role in the control of mRNA production.</pubmed_abstract><journal>PLoS computational biology</journal><pubmed_title>On the NF-Y regulome as in ENCODE (2019).</pubmed_title><pmcid>PMC7793273</pmcid><funding_grant_id>19050</funding_grant_id><pubmed_authors>Pavesi G</pubmed_authors><pubmed_authors>Dolfini D</pubmed_authors><pubmed_authors>Bernardini A</pubmed_authors><pubmed_authors>Mantovani R</pubmed_authors><pubmed_authors>Ronzio M</pubmed_authors></additional><is_claimable>false</is_claimable><name>On the NF-Y regulome as in ENCODE (2019).</name><description>NF-Y is a trimeric Transcription Factor -TF- which binds with high selectivity to the conserved CCAAT element. Individual ChIP-seq analysis as well as ENCODE have progressively identified locations shared by other TFs. Here, we have analyzed data introduced by ENCODE over the last five years in K562, HeLa-S3 and GM12878, including several chromatin features, as well RNA-seq profiling of HeLa cells after NF-Y inactivation. We double the number of sequence-specific TFs and co-factors reported. We catalogue them in 4 classes based on co-association criteria, infer target genes categorizations, identify positional bias of binding sites and gene expression changes. Larger and novel co-associations emerge, specifically concerning subunits of repressive complexes as well as RNA-binding proteins. On the one hand, these data better define NF-Y association with single members of major classes of TFs, on the other, they suggest that it might have a wider role in the control of mRNA production.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2024-11-21T10:40:58.521Z</modification><creation>2021-02-21T04:10:27Z</creation></dates><accession>S-EPMC7793273</accession><cross_references><pubmed>33370256</pubmed><doi>10.1371/journal.pcbi.1008488</doi></cross_references></HashMap>