Publication:
R Loops: From Physiological to Pathological Roles.

dc.contributor.authorGarcía-Muse, Tatiana
dc.contributor.authorAguilera, Andrés
dc.date.accessioned2023-02-08T14:37:24Z
dc.date.available2023-02-08T14:37:24Z
dc.date.issued2019-10-10
dc.description.abstractDNA-RNA hybrids play a physiological role in cellular processes, but often, they represent non-scheduled co-transcriptional structures with a negative impact on transcription, replication and DNA repair. Accumulating evidence suggests that they constitute a source of replication stress, DNA breaks and genome instability. Reciprocally, DNA breaks facilitate DNA-RNA hybrid formation by releasing the double helix torsional conformation. Cells avoid DNA-RNA accumulation by either preventing or removing hybrids directly or by DNA repair-coupled mechanisms. Given the R-loop impact on chromatin and genome organization and its potential relation with genetic diseases, we review R-loop homeostasis as well as their physiological and pathological roles.
dc.identifier.doi10.1016/j.cell.2019.08.055
dc.identifier.essn1097-4172
dc.identifier.pmid31607512
dc.identifier.unpaywallURLhttp://www.cell.com/article/S0092867419310062/pdf
dc.identifier.urihttp://hdl.handle.net/10668/14678
dc.issue.number3
dc.journal.titleCell
dc.journal.titleabbreviationCell
dc.language.isoen
dc.organizationCentro Andaluz de Biología Molecular y Medicina Regenerativa-CABIMER
dc.page.number604-618
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.pubmedtypeReview
dc.rights.accessRightsopen access
dc.subject.meshChromatin
dc.subject.meshDNA
dc.subject.meshDNA Breaks
dc.subject.meshDNA Repair
dc.subject.meshDNA Replication
dc.subject.meshGenomic Instability
dc.subject.meshHomeostasis
dc.subject.meshHumans
dc.subject.meshNucleic Acid Conformation
dc.subject.meshR-Loop Structures
dc.subject.meshRNA
dc.subject.meshTranscription, Genetic
dc.titleR Loops: From Physiological to Pathological Roles.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number179
dspace.entity.typePublication

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