Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
26
pubmed:dateCreated
2002-5-30
pubmed:abstractText
Telomerase is a regulated enzyme and its activity is tightly associated with cell proliferation. The mechanisms of this association are unclear, but specific growth factors may regulate telomerase activity. The present study examines the effect of epidermal growth factor (EGF) on telomerase activity and identifies the signal transduction pathway involved in this process. EGF up-regulated telomerase activity in EGF receptor-positive cells after the activation of telomerase reverse transcriptase (TERT) mRNA expression. This activation was rapid, peaked after 6 or 12 h and was not blocked by the concurrent exposure to cycloheximide, suggesting a direct effect of EGF on TERT transcription. Transient expression assays revealed that EGF activates the hTERT promoter and that the proximal core promoter is responsible for this regulation. The activation of hTERT mRNA expression by EGF was specifically blocked by MEK inhibitor, and in vitro kinase assays demonstrated that ERK is activated in response to EGF. Transient expression assays using mutant reporter plasmids revealed that an ETS motif located in the core promoter of hTERT is required for the EGF-induced transactivation of hTERT. Overexpression of wild type Ets in cells enhanced the EGF effect on hTERT transcription, while that of dominant negative Ets significantly repressed EGF action. These findings suggest that EGF activates telomerase through the direct activation of TERT transcription, in which the Ras/MEK/ERK pathway and Ets factor play major roles. Our data support the notion that growth factors directly regulate telomerase via specific signal transduction pathways.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Cycloheximide, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Protein Synthesis Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-ets, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/TERT protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Telomerase, http://linkedlifedata.com/resource/pubmed/chemical/Tert protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0950-9232
pubmed:author
pubmed:issnType
Print
pubmed:day
13
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4071-9
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12037663-3T3 Cells, pubmed-meshheading:12037663-Animals, pubmed-meshheading:12037663-Base Sequence, pubmed-meshheading:12037663-Cycloheximide, pubmed-meshheading:12037663-DNA Primers, pubmed-meshheading:12037663-DNA-Binding Proteins, pubmed-meshheading:12037663-Enzyme Activation, pubmed-meshheading:12037663-Enzyme Inhibitors, pubmed-meshheading:12037663-Epidermal Growth Factor, pubmed-meshheading:12037663-Humans, pubmed-meshheading:12037663-MAP Kinase Signaling System, pubmed-meshheading:12037663-Mice, pubmed-meshheading:12037663-Promoter Regions, Genetic, pubmed-meshheading:12037663-Protein Synthesis Inhibitors, pubmed-meshheading:12037663-Proto-Oncogene Proteins, pubmed-meshheading:12037663-Proto-Oncogene Proteins c-ets, pubmed-meshheading:12037663-RNA, Messenger, pubmed-meshheading:12037663-Telomerase, pubmed-meshheading:12037663-Transcription Factors, pubmed-meshheading:12037663-Transcriptional Activation
pubmed:year
2002
pubmed:articleTitle
Direct activation of telomerase by EGF through Ets-mediated transactivation of TERT via MAP kinase signaling pathway.
pubmed:affiliation
Department of Obstetrics and Gynecology, Kanazawa University, School of Medicine, 13-1, Takaramachi, Kanazawa, Ishikawa 920-8641, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't