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dc.contributor.authorDe La Cruz, C. C.en
dc.contributor.authorKirmizis, Antonisen
dc.contributor.authorSimon, M. D.en
dc.contributor.authorIsono, K. -Ien
dc.contributor.authorKoseki, H.en
dc.contributor.authorPanning, B.en
dc.creatorDe La Cruz, C. C.en
dc.creatorKirmizis, Antonisen
dc.creatorSimon, M. D.en
dc.creatorIsono, K. -Ien
dc.creatorKoseki, H.en
dc.creatorPanning, B.en
dc.date.accessioned2019-11-04T12:50:29Z
dc.date.available2019-11-04T12:50:29Z
dc.date.issued2007
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53041
dc.description.abstractRegulation of histone methylation is critical for proper gene expression and chromosome function. Suppressor of Zeste 12 (SUZ12) is a requisite member of the EED/EZH2 histone methyltransferase complexes, and is required for full activity of these complexes in vitro. In mammals and flies, SUZ12/Su(z)12 is necessary for trimethylation of histone H3 on lysine 27 (H3K27me3) on facultative heterochromatin. However, Su(z)12 is unique among Polycomb Group Proteins in that Su(z)12 mutant flies exhibit gross defects in position effect variegation, suggesting a role for Su(z)12 in constitutive heterochromatin formation. We investigated the role of Suz12 in constitutive heterochromatin and discovered that Suz12 is required for histone H3 lysine 9 tri-methylation (H3K9me3) in differentiated but not undifferentiated mouse embryonic stem cells. Knockdown of SUZ12 in human cells caused a reduction in H3K27me3 and H3K9me3, and altered the distribution of HP1α. In contrast, EZH2 knockdown caused loss of H3K27me3 but not H3K9me3, indicating that SUZ12 regulates H3-K9 methylation in an EZH2-independent fashion. This work uncovers a role for SUZ12 in H3-K9 methylation. © 2007 Springer.en
dc.sourceChromosome Researchen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-34248171732&doi=10.1007%2fs10577-007-1126-1&partnerID=40&md5=f76b34be4b2b6e5a8690800e80a84cd5
dc.subjectarticleen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectpriority journalen
dc.subjectmaleen
dc.subjectunclassified drugen
dc.subjectnonhumanen
dc.subjectproteinen
dc.subjecthuman cellen
dc.subjectAnimalsen
dc.subjectMiceen
dc.subjectanimal cellen
dc.subjectmouseen
dc.subjectTranscription Factorsen
dc.subjectDNA-Binding Proteinsen
dc.subjectcell differentiationen
dc.subjectprotein functionen
dc.subjectprotein localizationen
dc.subjectNuclear Proteinsen
dc.subjectProteinsen
dc.subjectRepressor Proteinsen
dc.subjectMammaliaen
dc.subjectCarrier Proteinsen
dc.subjectChromosomal Proteins, Non-Histoneen
dc.subjectDNA Methylationen
dc.subjectembryonic stem cellen
dc.subjectHeterochromatinen
dc.subjectheterochromatin protein 1en
dc.subjecthistone H3en
dc.subjectHistone methylationen
dc.subjectHistonesen
dc.subjectlysineen
dc.subjectmethylationen
dc.subjectPolycomb proteinen
dc.subjectsuppressor of zeste 12 proteinen
dc.subjectTissue Distributionen
dc.titleThe Polycomb Group Protein SUZ12 regulates histone H3 lysine 9 methylation and HP1α distributionen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1007/s10577-007-1126-1
dc.description.volume15
dc.description.startingpage299
dc.description.endingpage314
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 :26</p>en
dc.source.abbreviationChromosome Res.en
dc.contributor.orcidKirmizis, Antonis [0000-0002-3748-8711]
dc.gnosis.orcid0000-0002-3748-8711


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