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dc.contributor.authorAzmi, Ishara F.
dc.contributor.authorWatanabe, Shinya
dc.contributor.authorMaloney, Michael F.
dc.contributor.authorKang, Sukhyun
dc.contributor.authorBelsky, Jason A.
dc.contributor.authorMacAlpine, David M.
dc.contributor.authorPeterson, Craig L.
dc.contributor.authorBell, Stephen P.
dc.date2022-08-11T08:09:47.000
dc.date.accessioned2022-08-23T16:43:31Z
dc.date.available2022-08-23T16:43:31Z
dc.date.issued2017-03-21
dc.date.submitted2017-09-12
dc.identifier.citationElife. 2017 Mar 21;6. pii: e22512. doi: 10.7554/eLife.22512. <a href="https://doi.org/10.7554/eLife.22512">Link to article on publisher's site</a>
dc.identifier.issn2050-084X (Linking)
dc.identifier.doi10.7554/eLife.22512
dc.identifier.pmid28322723
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40311
dc.description.abstractEukaryotic replication origin licensing, activation and timing are influenced by chromatin but a mechanistic understanding is lacking. Using reconstituted nucleosomal DNA replication assays, we assessed the impact of nucleosomes on replication initiation. To generate distinct nucleosomal landscapes, different chromatin-remodeling enzymes (CREs) were used to remodel nucleosomes on origin-DNA templates. Nucleosomal organization influenced two steps of replication initiation: origin licensing and helicase activation. Origin licensing assays showed that local nucleosome positioning enhanced origin specificity and modulated helicase loading by influencing ORC DNA binding. Interestingly, SWI/SNF- and RSC-remodeled nucleosomes were permissive for origin licensing but showed reduced helicase activation. Specific CREs rescued replication of these templates if added prior to helicase activation, indicating a permissive chromatin state must be established during origin licensing to allow efficient origin activation. Our studies show nucleosomes directly modulate origin licensing and activation through distinct mechanisms and provide insights into the regulation of replication initiation by chromatin.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=28322723&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2017, Azmi et al.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectDNA Replication
dc.subjecteukaryotic
dc.subjecthelicase
dc.subjectS. cerevisiae
dc.subjectbiochemistry
dc.subjectchromatin remodeling enzyme
dc.subjectchromosomes
dc.subjectgenes
dc.subjectnucleosome
dc.subjectorigin licensing
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectCell and Developmental Biology
dc.subjectGenetics and Genomics
dc.titleNucleosomes influence multiple steps during replication initiation
dc.typeJournal Article
dc.source.journaltitleeLife
dc.source.volume6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4118&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3112
dc.identifier.contextkey10737543
refterms.dateFOA2022-08-23T16:43:31Z
html.description.abstract<p>Eukaryotic replication origin licensing, activation and timing are influenced by chromatin but a mechanistic understanding is lacking. Using reconstituted nucleosomal DNA replication assays, we assessed the impact of nucleosomes on replication initiation. To generate distinct nucleosomal landscapes, different chromatin-remodeling enzymes (CREs) were used to remodel nucleosomes on origin-DNA templates. Nucleosomal organization influenced two steps of replication initiation: origin licensing and helicase activation. Origin licensing assays showed that local nucleosome positioning enhanced origin specificity and modulated helicase loading by influencing ORC DNA binding. Interestingly, SWI/SNF- and RSC-remodeled nucleosomes were permissive for origin licensing but showed reduced helicase activation. Specific CREs rescued replication of these templates if added prior to helicase activation, indicating a permissive chromatin state must be established during origin licensing to allow efficient origin activation. Our studies show nucleosomes directly modulate origin licensing and activation through distinct mechanisms and provide insights into the regulation of replication initiation by chromatin.</p>
dc.identifier.submissionpathoapubs/3112
dc.contributor.departmentProgram in Molecular Medicine


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Copyright © 2017, Azmi et al.
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