dc.contributor.author | JnBaptiste, Courtney Kenneil | |
dc.contributor.author | Michaud, Joelle | |
dc.contributor.author | Praz, Viviane | |
dc.contributor.author | James Faresse, Nicole | |
dc.contributor.author | Tyagi, Shweta | |
dc.contributor.author | Schutz, Frederic | |
dc.contributor.author | Herr, Winship | |
dc.date.accessioned | 2013-12-13T15:01:32Z | |
dc.date.available | 2013-12-13T15:01:32Z | |
dc.date.issued | 2013-03 | |
dc.date.submitted | 2012-09 | |
dc.identifier.issn | 1088-9051 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/82917 | |
dc.description.abstract | In human transcriptional regulation, DNA-sequence-specific factors can associate with intermediaries that orchestrate interactions with a diverse set of chromatin-modifying enzymes. One such intermediary is HCFC1 (also known as HCF-1). HCFC1, first identified in herpes simplex virus transcription, has a poorly defined role in cellular transcriptional regulation. We show here that, in HeLa cells, HCFC1 is observed bound to 5400 generally active CpG-island promoters. Examination of the DNA sequences underlying the HCFC1-binding sites revealed three sequence motifs associated with the binding of (1) ZNF143 and THAP11 (also known as Ronin), (2) GABP, and (3) YY1 sequence-specific transcription factors. Subsequent analysis revealed colocalization of HCFC1 with these four transcription factors at ∼90% of the 5400 HCFC1-bound promoters. These studies suggest that a relatively small number of transcription factors play a major role in HeLa-cell transcriptional regulation in association with HCFC1. | en_US |
dc.language.iso | en_US | |
dc.publisher | Cold Spring Harbor Laboratory Press | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1101/gr.150078.112 | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/ | en_US |
dc.source | Cold Spring Harbor Laboratory Press | en_US |
dc.title | HCFC1 is a common component of active human CpG-island promoters and coincides with ZNF143, THAP11, YY1, and GABP transcription factor occupancy | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Michaud, J., V. Praz, N. James Faresse, C. K. JnBaptiste, S. Tyagi, F. Schutz, and W. Herr. “HCFC1 is a common component of active human CpG-island promoters and coincides with ZNF143, THAP11, YY1, and GABP transcription factor occupancy.” Genome Research 23, no. 6 (June 1, 2013): 907-916. © 2013, Published by Cold Spring Harbor Laboratory Press | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.mitauthor | JnBaptiste, Courtney Kenneil | en_US |
dc.relation.journal | Genome Research | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Michaud, J.; Praz, V.; James Faresse, N.; JnBaptiste, C. K.; Tyagi, S.; Schutz, F.; Herr, W. | en_US |
dc.identifier.orcid | https://orcid.org/0000-0001-8353-9316 | |
mit.license | PUBLISHER_CC | en_US |
mit.metadata.status | Complete | |