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dc.contributor.authorStokdyk, Kasey
dc.contributor.authorKim, Nayun
dc.contributor.authorOwiti, Norah Auma
dc.date.accessioned2018-10-31T19:52:35Z
dc.date.available2018-10-31T19:52:35Z
dc.date.issued2018-10
dc.date.submitted2018-10
dc.identifier.issn0172-8083
dc.identifier.issn1432-0983
dc.identifier.urihttp://hdl.handle.net/1721.1/118832
dc.description.abstractNon-canonical residue in DNA is a major and conserved source of genome instability. The appearance of uracil residues in DNA accompanies a significant mutagenic consequence and is regulated at multiple levels, from the concentration of available dUTP in the nucleotide pool to the excision repair for removal from DNA. Recently, an interesting phenomenon of transcription-associated elevation in uracil-derived mutations was described in Saccharomyces cerevisiae genome. While trying to understand the variability in mutagenesis, we uncovered that the frequency of uracil incorporation into DNA can vary depending on the transcription rate and that the non-replicative, repair-associated DNA synthesis underlies the higher uracil density of the actively transcribed genomic loci. This novel mechanism brings together the chemical vulnerability of DNA under transcription and the uracil-associated mutagenesis, and has the potential to apply to other non-canonical residues of mutagenic importance. Keyword: DNA repair; Non-canonical nucleotides; Transcription-associated mutagenesis; Uracil dUTPaseen_US
dc.publisherSpringer Berlin Heidelbergen_US
dc.relation.isversionofhttps://doi.org/10.1007/s00294-018-0895-8en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceSpringer Berlin Heidelbergen_US
dc.titleThe etiology of uracil residues in the Saccharomyces cerevisiae genomic DNAen_US
dc.typeArticleen_US
dc.identifier.citationOwiti, Norah et al. “The Etiology of Uracil Residues in the Saccharomyces Cerevisiae Genomic DNA.” Current Genetics (October 2018): 1-7 © 2018 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorOwiti, Norah Auma
dc.relation.journalCurrent Geneticsen_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.updated2018-10-18T04:01:35Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.orderedauthorsOwiti, Norah; Stokdyk, Kasey; Kim, Nayunen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5061-7434
mit.licensePUBLISHER_CCen_US


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