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R-Loops as Cellular Regulators and Genomic Threats.
Crossley, Madzia P; Bocek, Michael; Cimprich, Karlene A.
Affiliation
  • Crossley MP; Department of Chemical and Systems Biology, Stanford University School of Medicine, 318 Campus Drive, Stanford, CA 94305-5441, USA.
  • Bocek M; Department of Chemical and Systems Biology, Stanford University School of Medicine, 318 Campus Drive, Stanford, CA 94305-5441, USA.
  • Cimprich KA; Department of Chemical and Systems Biology, Stanford University School of Medicine, 318 Campus Drive, Stanford, CA 94305-5441, USA. Electronic address: cimprich@stanford.edu.
Mol Cell ; 73(3): 398-411, 2019 02 07.
Article in En | MEDLINE | ID: mdl-30735654
During transcription, the nascent RNA strand can base pair with its template DNA, displacing the non-template strand as ssDNA and forming a structure called an R-loop. R-loops are common across many domains of life and cause DNA damage in certain contexts. In this review, we summarize recent results implicating R-loops as important regulators of cellular processes such as transcription termination, gene regulation, and DNA repair. We also highlight recent work suggesting that R-loops can be problematic to cells as blocks to efficient transcription and replication that trigger the DNA damage response. Finally, we discuss how R-loops may contribute to cancer, neurodegeneration, and inflammatory diseases and compare the available next-generation sequencing-based approaches to map R-loops genome wide.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / RNA / Cell Nucleus / Genome / Genomic Instability / Nucleic Acid Heteroduplexes Limits: Animals / Humans Language: En Journal: Mol Cell Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA / RNA / Cell Nucleus / Genome / Genomic Instability / Nucleic Acid Heteroduplexes Limits: Animals / Humans Language: En Journal: Mol Cell Year: 2019 Document type: Article