Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2008-8-25
pubmed:abstractText
Retinoblastoma protein (pRB) mediates cell-cycle withdrawal and differentiation by interacting with a variety of proteins. RB-Binding Protein 2 (RBP2) has been shown to be a key effector. We sought to determine transcriptional regulation by RBP2 genome-wide by using location analysis and gene expression profiling experiments. We describe that RBP2 shows high correlation with the presence of H3K4me3 and its target genes are separated into two functionally distinct classes: differentiation-independent and differentiation-dependent genes. The former class is enriched by genes that encode mitochondrial proteins, while the latter is represented by cell-cycle genes. We demonstrate the role of RBP2 in mitochondrial biogenesis, which involves regulation of H3K4me3-modified nucleosomes. Analysis of expression changes upon RBP2 depletion depicted genes with a signature of differentiation control, analogous to the changes seen upon reintroduction of pRB. We conclude that, during differentiation, RBP2 exerts inhibitory effects on multiple genes through direct interaction with their promoters.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1097-4164
pubmed:author
pubmed:issnType
Electronic
pubmed:day
22
pubmed:volume
31
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
520-30
pubmed:dateRevised
2010-12-21
pubmed:meshHeading
pubmed-meshheading:18722178-Binding Sites, pubmed-meshheading:18722178-Cell Differentiation, pubmed-meshheading:18722178-Gene Expression Profiling, pubmed-meshheading:18722178-Gene Expression Regulation, pubmed-meshheading:18722178-Genome, Human, pubmed-meshheading:18722178-Genomics, pubmed-meshheading:18722178-Histones, pubmed-meshheading:18722178-Humans, pubmed-meshheading:18722178-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:18722178-Lysine, pubmed-meshheading:18722178-Methylation, pubmed-meshheading:18722178-Mitochondria, pubmed-meshheading:18722178-Models, Biological, pubmed-meshheading:18722178-Nucleosomes, pubmed-meshheading:18722178-Oxidoreductases, N-Demethylating, pubmed-meshheading:18722178-Promoter Regions, Genetic, pubmed-meshheading:18722178-Protein Binding, pubmed-meshheading:18722178-Repressor Proteins, pubmed-meshheading:18722178-Retinoblastoma-Binding Protein 2, pubmed-meshheading:18722178-Sequence Analysis, DNA, pubmed-meshheading:18722178-Transcription, Genetic, pubmed-meshheading:18722178-Transcription Factors, pubmed-meshheading:18722178-Tumor Suppressor Proteins
pubmed:year
2008
pubmed:articleTitle
Genome-wide analysis of the H3K4 histone demethylase RBP2 reveals a transcriptional program controlling differentiation.
pubmed:affiliation
Research Unit on Biomedical Informatics, Experimental and Health Science Department, Universitat Pompeu Fabra, Barcelona 08080, Spain.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural