Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5595
pubmed:dateCreated
2002-11-4
pubmed:abstractText
Polycomb group (PcG) proteins play important roles in maintaining the silent state of HOX genes. Recent studies have implicated histone methylation in long-term gene silencing. However, a connection between PcG-mediated gene silencing and histone methylation has not been established. Here we report the purification and characterization of an EED-EZH2 complex, the human counterpart of the Drosophila ESC-E(Z) complex. We demonstrate that the complex specifically methylates nucleosomal histone H3 at lysine 27 (H3-K27). Using chromatin immunoprecipitation assays, we show that H3-K27 methylation colocalizes with, and is dependent on, E(Z) binding at an Ultrabithorax (Ubx) Polycomb response element (PRE), and that this methylation correlates with Ubx repression. Methylation on H3-K27 facilitates binding of Polycomb (PC), a component of the PRC1 complex, to histone H3 amino-terminal tail. Thus, these studies establish a link between histone methylation and PcG-mediated gene silencing.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Chromatin, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/E(z) protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/EED protein, human, http://linkedlifedata.com/resource/pubmed/chemical/EZH2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Histone-Lysine N-Methyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Histones, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lysine, http://linkedlifedata.com/resource/pubmed/chemical/Methyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nucleosomes, http://linkedlifedata.com/resource/pubmed/chemical/PRC1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Polycomb protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/Protein Methyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Ubx protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/esc protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/histone methyltransferase
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1095-9203
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
298
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1039-43
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12351676-Animals, pubmed-meshheading:12351676-Carrier Proteins, pubmed-meshheading:12351676-Cell Cycle Proteins, pubmed-meshheading:12351676-Chromatin, pubmed-meshheading:12351676-DNA-Binding Proteins, pubmed-meshheading:12351676-Drosophila, pubmed-meshheading:12351676-Drosophila Proteins, pubmed-meshheading:12351676-Gene Silencing, pubmed-meshheading:12351676-Genes, Homeobox, pubmed-meshheading:12351676-HeLa Cells, pubmed-meshheading:12351676-Histone-Lysine N-Methyltransferase, pubmed-meshheading:12351676-Histones, pubmed-meshheading:12351676-Homeodomain Proteins, pubmed-meshheading:12351676-Humans, pubmed-meshheading:12351676-Lysine, pubmed-meshheading:12351676-Methylation, pubmed-meshheading:12351676-Methyltransferases, pubmed-meshheading:12351676-Nuclear Proteins, pubmed-meshheading:12351676-Nucleosomes, pubmed-meshheading:12351676-Peptide Mapping, pubmed-meshheading:12351676-Precipitin Tests, pubmed-meshheading:12351676-Protein Methyltransferases, pubmed-meshheading:12351676-Proteins, pubmed-meshheading:12351676-RNA Interference, pubmed-meshheading:12351676-Repressor Proteins, pubmed-meshheading:12351676-Response Elements, pubmed-meshheading:12351676-Temperature, pubmed-meshheading:12351676-Transcription Factors
pubmed:year
2002
pubmed:articleTitle
Role of histone H3 lysine 27 methylation in Polycomb-group silencing.
pubmed:affiliation
Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7295, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't