Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
16
pubmed:dateCreated
2003-4-14
pubmed:abstractText
Egr1, an immediate early transcription factor, responds to diverse stimuli and affects gene transcription to accomplish its biological effects. One important effect of Egr1 expression is to decrease the growth and tumorigenic potential of several tumor cell types. To identify important Egr1 target genes, we have adapted a methodology involving formaldehyde-induced protein-DNA cross-linking, chromatin immunoprecipitation, and multiplex PCR. Using this approach, we report the cloning of a new Egr1 target gene that is able to account, at least in part, for the growth inhibitory activity of Egr1. We have named this new protein TOE1 for target of Egr1.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Chromatin, http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents, http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/EGR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Early Growth Response Protein 1, http://linkedlifedata.com/resource/pubmed/chemical/Formaldehyde, http://linkedlifedata.com/resource/pubmed/chemical/Immediate-Early Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Luciferases, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/TGFB1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
18
pubmed:volume
278
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
14306-12
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12562764-Blotting, Northern, pubmed-meshheading:12562764-Chromatin, pubmed-meshheading:12562764-Cloning, Molecular, pubmed-meshheading:12562764-Cross-Linking Reagents, pubmed-meshheading:12562764-DNA, pubmed-meshheading:12562764-DNA, Complementary, pubmed-meshheading:12562764-DNA-Binding Proteins, pubmed-meshheading:12562764-Early Growth Response Protein 1, pubmed-meshheading:12562764-Flow Cytometry, pubmed-meshheading:12562764-Formaldehyde, pubmed-meshheading:12562764-Gene Library, pubmed-meshheading:12562764-Humans, pubmed-meshheading:12562764-Immediate-Early Proteins, pubmed-meshheading:12562764-Luciferases, pubmed-meshheading:12562764-Microscopy, Confocal, pubmed-meshheading:12562764-Microscopy, Fluorescence, pubmed-meshheading:12562764-Nuclear Proteins, pubmed-meshheading:12562764-Polymerase Chain Reaction, pubmed-meshheading:12562764-Precipitin Tests, pubmed-meshheading:12562764-Promoter Regions, Genetic, pubmed-meshheading:12562764-Protein Binding, pubmed-meshheading:12562764-Proteins, pubmed-meshheading:12562764-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12562764-Transcription, Genetic, pubmed-meshheading:12562764-Transcription Factors, pubmed-meshheading:12562764-Transcriptional Activation, pubmed-meshheading:12562764-Transfection, pubmed-meshheading:12562764-Transforming Growth Factor beta, pubmed-meshheading:12562764-Transforming Growth Factor beta1
pubmed:year
2003
pubmed:articleTitle
In vivo cloning and characterization of a new growth suppressor protein TOE1 as a direct target gene of Egr1.
pubmed:affiliation
Burnham Institute, La Jolla Cancer Research Center, California 92037, USA. idebelle@burnham.org
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't