Show simple item record

dc.contributor.authorGuenther, Matthew G.
dc.contributor.authorLevine, Stuart S.
dc.contributor.authorBoyer, Laurie A.
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorYoung, Richard A.
dc.date2022-08-11T08:08:58.000
dc.date.accessioned2022-08-23T16:14:01Z
dc.date.available2022-08-23T16:14:01Z
dc.date.issued2007-07-17
dc.date.submitted2008-09-18
dc.identifier.citationCell. 2007 Jul 13;130(1):77-88. <a href="http://dx.doi.org/10.1016/j.cell.2007.05.042">Link to article on publisher's site</a>
dc.identifier.issn0092-8674 (Print)
dc.identifier.doi10.1016/j.cell.2007.05.042
dc.identifier.pmid17632057
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33763
dc.description.abstractWe describe the results of a genome-wide analysis of human cells that suggests that most protein-coding genes, including most genes thought to be transcriptionally inactive, experience transcription initiation. We found that nucleosomes with H3K4me3 and H3K9,14Ac modifications, together with RNA polymerase II, occupy the promoters of most protein-coding genes in human embryonic stem cells. Only a subset of these genes produce detectable full-length transcripts and are occupied by nucleosomes with H3K36me3 modifications, a hallmark of elongation. The other genes experience transcription initiation but show no evidence of elongation, suggesting that they are predominantly regulated at postinitiation steps. Genes encoding most developmental regulators fall into this group. Our results also identify a class of genes that are excluded from experiencing transcription initiation, at which mechanisms that prevent initiation must predominate. These observations extend to differentiated cells, suggesting that transcription initiation at most genes is a general phenomenon in human cells.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17632057&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.cell.2007.05.042
dc.subjectCell Differentiation; Cells, Cultured; Chromatin; Chromatin Immunoprecipitation; DNA Methylation; Embryonic Stem Cells; Gene Expression Regulation; Histones; Humans; Lysine; Multigene Family; Nucleosomes; Oligonucleotide Array Sequence Analysis; *Promoter Regions (Genetics); RNA Polymerase II; *Transcription Initiation Site; *Transcription, Genetic
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleA chromatin landmark and transcription initiation at most promoters in human cells
dc.typeJournal Article
dc.source.journaltitleCell
dc.source.volume130
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/423
dc.identifier.contextkey632661
html.description.abstract<p>We describe the results of a genome-wide analysis of human cells that suggests that most protein-coding genes, including most genes thought to be transcriptionally inactive, experience transcription initiation. We found that nucleosomes with H3K4me3 and H3K9,14Ac modifications, together with RNA polymerase II, occupy the promoters of most protein-coding genes in human embryonic stem cells. Only a subset of these genes produce detectable full-length transcripts and are occupied by nucleosomes with H3K36me3 modifications, a hallmark of elongation. The other genes experience transcription initiation but show no evidence of elongation, suggesting that they are predominantly regulated at postinitiation steps. Genes encoding most developmental regulators fall into this group. Our results also identify a class of genes that are excluded from experiencing transcription initiation, at which mechanisms that prevent initiation must predominate. These observations extend to differentiated cells, suggesting that transcription initiation at most genes is a general phenomenon in human cells.</p>
dc.identifier.submissionpathgsbs_sp/423
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages77-88


Files in this item

Thumbnail
Name:
Publisher version

This item appears in the following Collection(s)

Show simple item record