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dc.contributor.authorXu, Jia
dc.contributor.authorYanagisawa, Yoshimi
dc.contributor.authorTsankov, Alexander M
dc.contributor.authorHart, Christopher
dc.contributor.authorAoki, Keita
dc.contributor.authorKommajosyula, Naveen
dc.contributor.authorSteinmann, Kathleen E.
dc.contributor.authorBochicchio, James
dc.contributor.authorRuss, Carsten
dc.contributor.authorRegev, Aviv
dc.contributor.authorRando, Oliver J
dc.contributor.authorNusbaum, Chad
dc.contributor.authorNiki, Hironori
dc.contributor.authorMilos, Patrice M.
dc.contributor.authorWeng, Zhiping
dc.contributor.authorRhind, Nicholas
dc.contributor.authorRegev, Aviv
dc.date.accessioned2012-05-25T17:48:47Z
dc.date.available2012-05-25T17:48:47Z
dc.date.issued2012-04
dc.date.submitted2012-03
dc.identifier.issn1465-6906
dc.identifier.issn1474-7596
dc.identifier.urihttp://hdl.handle.net/1721.1/70949
dc.description.abstractBackground DNA replication initiates at distinct origins in eukaryotic genomes, but the genomic features that define these sites are not well understood. Results We have taken a combined experimental and bioinformatic approach to identify and characterize origins of replication in three distantly related fission yeasts: Schizosaccharomyces pombe, Schizosaccharomyces octosporus and Schizosaccharomyces japonicus. Using single-molecule deep sequencing to construct amplification-free high-resolution replication profiles, we located origins and identified sequence motifs that predict origin function. We then mapped nucleosome occupancy by deep sequencing of mononucleosomal DNA from the corresponding species, finding that origins tend to occupy nucleosome-depleted regions. Conclusions The sequences that specify origins are evolutionarily plastic, with low complexity nucleosome-excluding sequences functioning in S. pombe and S. octosporus, and binding sites for trans-acting nucleosome-excluding proteins functioning in S. japonicus. Furthermore, chromosome-scale variation in replication timing is conserved independently of origin location and via a mechanism distinct from known heterochromatic effects on origin function. These results are consistent with a model in which origins are simply the nucleosome-depleted regions of the genome with the highest affinity for the origin recognition complex. This approach provides a general strategy for understanding the mechanisms that define DNA replication origins in eukaryotes.en_US
dc.description.sponsorshipAmerican Cancer Society (Research Scholar Grant)en_US
dc.publisherSpringer (Biomed Central Ltd.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/gb-2012-13-4-r27en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleGenome-wide identification and characterization of replication origins by deep sequencingen_US
dc.typeArticleen_US
dc.identifier.citationXu, Jia et al. “Genome-wide Identification and Characterization of Replication Origins by Deep Sequencing.” Genome Biology 13.4 (2012): R27. Web. 25 May 2012.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.approverRegev, Aviv
dc.contributor.mitauthorRegev, Aviv
dc.relation.journalGenome Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2012-05-25T15:04:21Z
dc.language.rfc3066en
dc.rights.holderXu et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsXu, Jia; Yanagisawa, Yoshimi; Tsankov, Alexander M; Hart, Christopher; Aoki, Keita; Kommajosyula, Naveen; Steinmann, Kathleen E; Bochicchio, James; Russ, Carsten; Regev, Aviv; Rando, Oliver J; Nusbaum, Chad; Niki, Hironori; Milos, Patrice; Weng, Zhiping; Rhind, Nicholasen
dc.identifier.orcidhttps://orcid.org/0000-0001-8567-2049
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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