Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/120404
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dc.contributor.authorSolé, Anna-
dc.contributor.authorDelagoutte, Emmanuelle-
dc.contributor.authorCiudad i Gómez, Carlos Julián-
dc.contributor.authorNoé Mata, Verónica-
dc.contributor.authorAlberti, Patrizia-
dc.date.accessioned2018-03-02T14:59:52Z-
dc.date.available2018-03-02T14:59:52Z-
dc.date.issued2017-01-09-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2445/120404-
dc.description.abstractPolypurine reverse-Hoogsteen (PPRH) oligonucleotides are non-modified DNA molecules composed of two mirror-symmetrical polypurine stretches linked by a five-thymidine loop. They can fold into reverse-Hoogsteen hairpins and bind to their polypyrimidine target sequence by Watson-Crick bonds forming a three-stranded structure. They have been successfully used to knockdown gene expression and to repair single-point mutations in cells. In this work, we provide an in vitro characterization (UV and fluorescence spectroscopy, gel electrophoresis and nuclease assays) of the structure and stability of two repair-PPRH oligonucleotides and of the complexes they form with their single-stranded targets. We show that one PPRH oligonucleotide forms a hairpin, while the other folds, in potassium, into a guanine-quadruplex (G4). However, the hairpin-prone oligonucleotide does not form a triplex with its single-stranded target, while the G4-prone oligonucleotide converts from a G4 into a reverse-Hoogsteen hairpin forming a triplex with its target sequence. Our work proves, in particular, that folding of a PPRH oligonucleotide into a G4 does not necessarily impair sequence-specific DNA recognition by triplex formation. It also illustrates an original example of DNA structural conversion of a G4 into a reverse-Hoogsteen hairpin driven by triplex formation; this kind of conversion might occur at particular loci of genomic DNA.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherNature Publishing Group-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/srep39898-
dc.relation.ispartofScientific Reports, 2017, vol. 7 , num. 39898-
dc.relation.urihttps://doi.org/10.1038/srep39898-
dc.rightscc-by (c) Solé, Anna et al., 2017-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.subject.classificationADN-
dc.subject.classificationEstructura molecular-
dc.subject.otherDNA-
dc.subject.otherMolecular structure-
dc.titlePolypurine reverse-Hoogsteen (PPRH) oligonucleotides can form triplexes with their target sequences even under conditions where they fold into G-quadruplexes-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec670332-
dc.date.updated2018-03-02T14:59:52Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Bioquímica i Fisiologia)

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