Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2010-11-15
pubmed:databankReference
pubmed:abstractText
Cell differentiation requires remodeling of tissue-specific gene loci and activities of key transcriptional regulators, which are recognized for their dominant control over cellular programs. Using epigenomic methods, we characterized enhancer elements specifically modified in differentiating intestinal epithelial cells and found enrichment of transcription factor-binding motifs corresponding to CDX2, a critical regulator of the intestine. Directed investigation revealed surprising lability in CDX2 occupancy of the genome, with redistribution from hundreds of sites occupied only in proliferating cells to thousands of new sites in differentiated cells. Knockout mice confirmed distinct Cdx2 requirements in dividing and mature adult intestinal cells, including responsibility for the active enhancer configuration associated with maturity. Dynamic CDX2 occupancy corresponds with condition-specific gene expression and, importantly, to differential co-occupancy with other tissue-restricted transcription factors, such as GATA6 and HNF4A. These results reveal dynamic, context-specific functions and mechanisms of a prominent transcriptional regulator within a cell lineage. VIDEO ABSTRACT:
pubmed:grant
http://linkedlifedata.com/resource/pubmed/grant/K01 DK088868-02, http://linkedlifedata.com/resource/pubmed/grant/P50 CA127003-04, http://linkedlifedata.com/resource/pubmed/grant/R01 DK054111-12, http://linkedlifedata.com/resource/pubmed/grant/R01 DK054111-14, http://linkedlifedata.com/resource/pubmed/grant/R01 DK082889-01A1, http://linkedlifedata.com/resource/pubmed/grant/R01 DK082889-02, http://linkedlifedata.com/resource/pubmed/grant/R01 HG004069-05, http://linkedlifedata.com/resource/pubmed/grant/R01 HL063143-13, http://linkedlifedata.com/resource/pubmed/grant/R01DK054111, http://linkedlifedata.com/resource/pubmed/grant/R01DK082889, http://linkedlifedata.com/resource/pubmed/grant/R01HG004069, http://linkedlifedata.com/resource/pubmed/grant/RC2 CA148222-01, http://linkedlifedata.com/resource/pubmed/grant/RC2CA148222, http://linkedlifedata.com/resource/pubmed/grant/T32DK07477
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1878-1551
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
16
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
713-26
pubmed:dateRevised
2011-11-9
pubmed:meshHeading
pubmed-meshheading:21074721-Animals, pubmed-meshheading:21074721-Base Sequence, pubmed-meshheading:21074721-Caco-2 Cells, pubmed-meshheading:21074721-Cell Differentiation, pubmed-meshheading:21074721-Cell Proliferation, pubmed-meshheading:21074721-Chromatin, pubmed-meshheading:21074721-Enhancer Elements, Genetic, pubmed-meshheading:21074721-Epigenomics, pubmed-meshheading:21074721-Epithelial Cells, pubmed-meshheading:21074721-GATA6 Transcription Factor, pubmed-meshheading:21074721-Gene Expression Regulation, Developmental, pubmed-meshheading:21074721-Genome, pubmed-meshheading:21074721-Hepatocyte Nuclear Factor 4, pubmed-meshheading:21074721-Histones, pubmed-meshheading:21074721-Homeodomain Proteins, pubmed-meshheading:21074721-Humans, pubmed-meshheading:21074721-Intestines, pubmed-meshheading:21074721-Mice, pubmed-meshheading:21074721-Mice, Knockout, pubmed-meshheading:21074721-Molecular Sequence Data, pubmed-meshheading:21074721-Trans-Activators, pubmed-meshheading:21074721-Transcription Factors
pubmed:year
2010
pubmed:articleTitle
Differentiation-specific histone modifications reveal dynamic chromatin interactions and partners for the intestinal transcription factor CDX2.
pubmed:affiliation
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural