i-motif structures in long cytosine-rich sequences found upstream of the promoter region of the SMARCA4 gen

dc.contributor.authorBenabou Zdaou, Sanae
dc.contributor.authorAviñó Andrés, Anna
dc.contributor.authorLyonnais, Sébastien
dc.contributor.authorGonzález, Carlos
dc.contributor.authorEritja i Casadellà, Ramon
dc.contributor.authorJuan Capdevila, Anna de
dc.contributor.authorGargallo Gómez, Raimundo
dc.date.accessioned2017-06-19T12:08:09Z
dc.date.available2018-06-12T22:01:23Z
dc.date.issued2017-06-12
dc.date.updated2017-06-19T12:08:09Z
dc.description.abstractCytosine-rich oligonucleotides are capable of forming complex structures known as i-motif with increasingly studied biological properties. The study of sequences prone to form i-motifs located near the promoter region of genes may be difficult because these sequences not only contain repeats of cytosine tracts of disparate length but also these may be separated by loops of varied nature and length. In this work, the formation of an intramolecular i-motif structures by a long sequence located upstream of the promoter region of the SMARCA4 gene has been demonstrated. Nuclear Magnetic Resonance, Circular Dichroism, Gel Electrophoresis, Size-Exclusion Chromatography, and multivariate analysis have been used. Not only the wild sequence (5'-TC3T2GCTATC3TGTC2TGC2TCGC3T2G2TCATGA2C4-3') has been studied but also several other truncated and mutated sequences. Despite the apparent complex sequence, the results showed that the wild sequence may form a relatively stable and homogeneous unimolecular i-motif structure, both in terms of pH or temperature. The model ligand TMPyP4 destabilizes the structure, whereas the presence of 20% (w/v) PEG200 stabilized it slightly. This finding opens the door to the study of the interaction of these kind of i-motif structures with stabilizing ligands or proteins.
dc.format.extent65 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec672223
dc.identifier.issn0300-9084
dc.identifier.pmid28619677
dc.identifier.urihttps://hdl.handle.net/2445/112556
dc.language.isoeng
dc.publisherElsevier Masson SAS
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.biochi.2017.06.005
dc.relation.ispartofBiochimie, 2017, vol. 140, p. 20-33
dc.relation.urihttps://doi.org/10.1016/j.biochi.2017.06.005
dc.rightscc by-nc-nd (c) Elsevier Masson SAS, 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.sourceArticles publicats en revistes (Enginyeria Química i Química Analítica)
dc.subject.classificationLligands
dc.subject.classificationOligonucleòtids
dc.subject.classificationADN
dc.subject.classificationRessonància magnètica nuclear
dc.subject.classificationCromatografia
dc.subject.classificationAnàlisi multivariable
dc.subject.otherLigands
dc.subject.otherOligonucleotides
dc.subject.otherDNA
dc.subject.otherNuclear magnetic resonance
dc.subject.otherChromatography
dc.subject.otherMultivariate analysis
dc.titlei-motif structures in long cytosine-rich sequences found upstream of the promoter region of the SMARCA4 gen
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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