Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19259
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dc.contributor.authorDialynas, G. K.en
dc.contributor.authorTerjung, S.en
dc.contributor.authorBrown, J. P.en
dc.contributor.authorAucott, R. L.en
dc.contributor.authorBaron-Luhr, B.en
dc.contributor.authorSingh, P. B.en
dc.contributor.authorGeorgatos, S. D.en
dc.date.accessioned2015-11-24T18:58:14Z-
dc.date.available2015-11-24T18:58:14Z-
dc.identifier.issn0021-9533-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19259-
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectCell Lineen
dc.subjectChromosomal Proteins, Non-Histone/genetics/*metabolismen
dc.subjectEpithelial Cells/cytology/*physiologyen
dc.subjectFibroblasts/cytology/*physiologyen
dc.subjectHeterochromatin/metabolismen
dc.subjectHumansen
dc.subjectMiceen
dc.subjectPluripotent Stem Cells/cytology/*physiologyen
dc.subjectProtein Isoforms/genetics/*metabolismen
dc.subjectRecombinant Fusion Proteins/genetics/metabolismen
dc.titlePlasticity of HP1 proteins in mammalian cellsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1242/jcs.012914-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17855382-
heal.identifier.secondaryhttp://jcs.biologists.org/content/120/19/3415.full.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2007-
heal.abstractWe have compared the distribution of endogenous heterochromatin protein 1 (HP1) proteins (alpha, beta and gamma) in different epithelial lines, pluripotent stem cells and embryonic fibroblasts. In parallel, we have interrogated assembly and dynamics of newly expressed HP1-GFP proteins in cells lacking both HP1alpha and HP1beta alleles, blocked at the G1-S boundary, or cultured in the presence of HDAC and HAT inhibitors. The results reveal a range of cell type and differentiation state-specific patterns that do not correlate with 'fast' or 'slow' subunit exchange in heterochromatin. Furthermore, our observations show that targeting of HP1gamma to heterochromatic sites depends on HP1alpha and H1beta and that, on an architectural level, HP1alpha is the most polymorphic variant of the HP1 family. These data provide evidence for HP1 plasticity under shifting microenvironmental conditions and offer a new conceptual framework for understanding chromatin dynamics at the molecular level.en
heal.journalNameJ Cell Scien
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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