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dc.contributor.authorMarion, R. M.en
dc.contributor.authorStrati, Katerinaen
dc.contributor.authorLi, H.en
dc.contributor.authorTejera, A.en
dc.contributor.authorSchoeftner, S.en
dc.contributor.authorOrtega, S.en
dc.contributor.authorSerrano, M.en
dc.contributor.authorBlasco, M. A.en
dc.creatorMarion, R. M.en
dc.creatorStrati, Katerinaen
dc.creatorLi, H.en
dc.creatorTejera, A.en
dc.creatorSchoeftner, S.en
dc.creatorOrtega, S.en
dc.creatorSerrano, M.en
dc.creatorBlasco, M. A.en
dc.date.accessioned2019-11-04T12:52:19Z
dc.date.available2019-11-04T12:52:19Z
dc.date.issued2009
dc.identifier.issn1934-5909
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53239
dc.description.abstractTelomere shortening is associated with organismal aging. iPS cells have been recently derived from old patientsen
dc.description.abstracthowever, it is not known whether telomere chromatin acquires the same characteristics as in ES cells. We show here that telomeres are elongated in iPS cells compared to the parental differentiated cells both when using four (Oct3/4, Sox2, Klf4, cMyc) or three (Oct3/4, Sox2, Klf4) reprogramming factors and both from young and aged individuals. We demonstrate genetically that, during reprogramming, telomere elongation is usually mediated by telomerase and that iPS telomeres acquire the epigenetic marks of ES cells, including a low density of trimethylated histones H3K9 and H4K20 and increased abundance of telomere transcripts. Finally, reprogramming efficiency of cells derived from increasing generations of telomerase-deficient mice shows a dramatic decrease in iPS cell efficiency, a defect that is restored by telomerase reintroduction. Together, these results highlight the importance of telomere biology for iPS cell generation and functionality. © 2009 Elsevier Inc. All rights reserved.en
dc.sourceCell Stem Cellen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-58949094552&doi=10.1016%2fj.stem.2008.12.010&partnerID=40&md5=7197d1fb9ce38b54dbb37b030e1ad686
dc.subjectarticleen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectcontrolled studyen
dc.subjectpriority journalen
dc.subjectAgingen
dc.subjectage distributionen
dc.subjectunclassified drugen
dc.subjectnonhumanen
dc.subjecthuman cellen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal cellen
dc.subjectanimal experimenten
dc.subjectmouseen
dc.subjectPluripotent Stem Cellsen
dc.subjectcell differentiationen
dc.subjectenzyme activityen
dc.subjectProto-Oncogene Proteins c-mycen
dc.subjectepigeneticsen
dc.subjectFibroblastsen
dc.subjectMusen
dc.subjectembryoen
dc.subjectEnzyme Activationen
dc.subjectMice, Knockouten
dc.subjectCells, Cultureden
dc.subjectembryonic stem cellen
dc.subjectcell lineen
dc.subjectinduced pluripotent stem cellen
dc.subjectpluripotent stem cellen
dc.subjectkruppel like factor 4en
dc.subjectnuclear reprogrammingen
dc.subjectoctamer transcription factor 4en
dc.subjecttranscription factor Sox2en
dc.subjecthistoneen
dc.subjectEmbryonic Stem Cellsen
dc.subjectIpsen
dc.subjectMice, Inbred C57BLen
dc.subjecttelomereen
dc.subjectchromosome sizeen
dc.subjecthistone h3k9en
dc.subjecthistone H4K20en
dc.subjectMyc proteinen
dc.subjectSTEMCELLen
dc.subjecttelomeraseen
dc.subjectTransplantation Chimeraen
dc.titleTelomeres Acquire Embryonic Stem Cell Characteristics in Induced Pluripotent Stem Cellsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.stem.2008.12.010
dc.description.volume4
dc.description.startingpage141
dc.description.endingpage154
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :271</p>en
dc.source.abbreviationCell Stem Cellen
dc.contributor.orcidStrati, Katerina [0000-0002-2332-787X]
dc.gnosis.orcid0000-0002-2332-787X


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