Nucleosome stability measured in situ by automated quantitative imaging

dc.contributor.authorImre, László
dc.contributor.authorSimándi, Zoltán
dc.contributor.authorHorváth, Attila
dc.contributor.authorFenyőfalvi, György
dc.contributor.authorNánási, Péter
dc.contributor.authorNiaki, Erfaneh Firouzi
dc.contributor.authorHegedüs, Éva
dc.contributor.authorBacsó, Zsolt
dc.contributor.authorWeyemi, Urbain
dc.contributor.authorMauser, Rebekka
dc.contributor.authorAusió, Juan
dc.contributor.authorJeltsch, Albert
dc.contributor.authorBonner, William
dc.contributor.authorNagy, László
dc.contributor.authorKimura, Hiroshi
dc.contributor.authorSzabó, Gábor
dc.date.accessioned2019-01-24T20:23:02Z
dc.date.available2019-01-24T20:23:02Z
dc.date.copyright2017en_US
dc.date.issued2017
dc.description.abstractCurrent approaches have limitations in providing insight into the functional properties of particular nucleosomes in their native molecular environment. Here we describe a simple and powerful method involving elution of histones using intercalators or salt, to assess stability features dependent on DNA superhelicity and relying mainly on electrostatic interactions, respectively, and measurement of the fraction of histones remaining chromatin-bound in the individual nuclei using histone type- or posttranslational modification- (PTM-) specific antibodies and automated, quantitative imaging. The method has been validated in H3K4me3 ChIP-seq experiments, by the quantitative assessment of chromatin loop relaxation required for nucleosomal destabilization, and by comparative analyses of the intercalator and salt induced release from the nucleosomes of different histones. The accuracy of the assay allowed us to observe examples of strict association between nucleosome stability and PTMs across cell types, differentiation state and throughout the cell-cycle in close to native chromatin context, and resolve ambiguities regarding the destabilizing effect of H2A.X phosphorylation. The advantages of the in situ measuring scenario are demonstrated via the marked effect of DNA nicking on histone eviction that underscores the powerful potential of topological relaxation in the epigenetic regulation of DNA accessibility.en_US
dc.description.reviewstatusRevieweden_US
dc.description.scholarlevelFacultyen_US
dc.description.sponsorshipThe authors thank Adel Nagy Vezendine for conscientious technical assistance and Katrina Good for a careful proofreading of the manuscript. We thank Tom Misteli, NIH, for providing the LacO array system. This work was supported by Hungarian National Science and Research Foundation (OTKA) grants [K72762]; [NK101337]; by TAMOP grants [TAMOP 4.2.2-08/1-2008-0015], [TAMOP 4.2.1/B-09/1/KONV-2010-0007], [TAMOP 4.2.2.A-11/1/KONV-2012-0023 "VED-ELEM"], and [TAMOP 4.2.4.A/2-11-1-2012-0001, GINOP-2.3.2-15-2016-00044, National Excellence Program]', by JSPS KAKENHI, JP 25116005, JP26291071 (to HK) and by Natural Sciences and Engeneering Research Council of Canada (NSERC) 46399-2012 grant (to JA).en_US
dc.identifier.citationImre, L.; Simándi, Z.; Horváth, A.; Fenyőfalvi, G.; Nánási, P.; Niaki, E. F.; … & Szabó, G. Nucleosome stability measured in situ by automated quantitative imaging. Scientific Reports, 7, article 12734. DOI: 10.1038/s41598-017-12608-9en_US
dc.identifier.urihttps://doi.org/10.1038/s41598-017-12608-9
dc.identifier.urihttp://hdl.handle.net/1828/10548
dc.language.isoenen_US
dc.publisherScientific Reportsen_US
dc.subject.departmentDepartment of Biochemistry and Microbiology
dc.titleNucleosome stability measured in situ by automated quantitative imagingen_US
dc.typeArticleen_US

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