Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2010-2-12
pubmed:abstractText
Poly(ADP-ribosyl)ation of the conserved multifunctional transcription factor CTCF was previously identified as important to maintain CTCF insulator and chromatin barrier functions. However, the molecular mechanism of this regulation and also the necessity of this modification for other CTCF functions remain unknown. In this study, we identified potential sites of poly(ADP-ribosyl)ation within the N-terminal domain of CTCF and generated a mutant deficient in poly(ADP-ribosyl)ation. Using this CTCF mutant, we demonstrated the requirement of poly(ADP-ribosyl)ation for optimal CTCF function in transcriptional activation of the p19ARF promoter and inhibition of cell proliferation. By using a newly generated isogenic insulator reporter cell line, the CTCF insulator function at the mouse Igf2-H19 imprinting control region (ICR) was found to be compromised by the CTCF mutation. The association and simultaneous presence of PARP-1 and CTCF at the ICR, confirmed by single and serial chromatin immunoprecipitation assays, were found to be independent of CTCF poly(ADP-ribosyl)ation. These results suggest a model of CTCF regulation by poly(ADP-ribosyl)ation whereby CTCF and PARP-1 form functional complexes at sites along the DNA, producing a dynamic reversible modification of CTCF. By using bioinformatics tools, numerous sites of CTCF and PARP-1 colocalization were demonstrated, suggesting that such regulation of CTCF may take place at the genome level.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CCCTC-binding factor, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/H19 long non-coding RNA, http://linkedlifedata.com/resource/pubmed/chemical/IGF2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor II, http://linkedlifedata.com/resource/pubmed/chemical/PARP1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Poly(ADP-ribose) Polymerases, http://linkedlifedata.com/resource/pubmed/chemical/Poly Adenosine Diphosphate Ribose, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Untranslated, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1098-5549
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1199-216
pubmed:dateRevised
2011-10-7
pubmed:meshHeading
pubmed-meshheading:20038529-Amino Acid Sequence, pubmed-meshheading:20038529-Amino Acid Substitution, pubmed-meshheading:20038529-Animals, pubmed-meshheading:20038529-Base Sequence, pubmed-meshheading:20038529-Binding Sites, pubmed-meshheading:20038529-Cell Line, pubmed-meshheading:20038529-Cell Proliferation, pubmed-meshheading:20038529-DNA Primers, pubmed-meshheading:20038529-Genomic Imprinting, pubmed-meshheading:20038529-HeLa Cells, pubmed-meshheading:20038529-Humans, pubmed-meshheading:20038529-Hybrid Cells, pubmed-meshheading:20038529-Insulin-Like Growth Factor II, pubmed-meshheading:20038529-Mice, pubmed-meshheading:20038529-Molecular Sequence Data, pubmed-meshheading:20038529-Mutagenesis, Site-Directed, pubmed-meshheading:20038529-Mutation, pubmed-meshheading:20038529-Poly(ADP-ribose) Polymerases, pubmed-meshheading:20038529-Poly Adenosine Diphosphate Ribose, pubmed-meshheading:20038529-RNA, Untranslated, pubmed-meshheading:20038529-Recombinant Proteins, pubmed-meshheading:20038529-Repressor Proteins, pubmed-meshheading:20038529-Transfection
pubmed:year
2010
pubmed:articleTitle
Mutational analysis of the poly(ADP-ribosyl)ation sites of the transcription factor CTCF provides an insight into the mechanism of its regulation by poly(ADP-ribosyl)ation.
pubmed:affiliation
Department of Biological Sciences, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, United Kingdom.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't