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Resolution of ROS‐induced G‐quadruplexes and R‐loops at transcriptionally active sites is dependent on BLM helicase

Jun Jie Tan, Xiangyu Wang, Laiyee Phoon, Haibo Yang, Li Lan

2020FEBS Letters55 citationsDOI

Abstract

R-loops and G-quadruplexes (G4s) are noncanonical secondary DNA structures. Here, we show that reactive oxygen species (ROS) induce G4 formation as well as R-loops at transcriptionally active sites. Importantly, the G4 structure is subsequently triggered by R-loop formation after damage. Once G4 is formed within an R-loop, it reversely stabilizes the R-loop. Notably, the helicase activity of Bloom syndrome protein is essential for the resolution of both R-loops and G4s. Unresolved G4s and R-loops delay the repair of ROS-induced damage at actively transcribed sites. Together, our results demonstrate that interregulation between R-loops and G4s induced by ROS is essential for repair at transcriptionally active sites.

Topics & Concepts

HelicaseResolution (logic)ChemistryG-quadruplexCell biologyBiophysicsRNA Helicase AMolecular biologyPhysicsBiologyDNABiochemistryGeneComputer scienceRNAArtificial intelligenceDNA and Nucleic Acid ChemistryAdvanced biosensing and bioanalysis techniquesRNA and protein synthesis mechanisms
Resolution of ROS‐induced G‐quadruplexes and R‐loops at transcriptionally active sites is dependent on BLM helicase | Litcius