Detection and Characterization of R Loop Structures

Methods Mol Biol. 2017:1543:231-242. doi: 10.1007/978-1-4939-6716-2_13.

Abstract

R loops are special three stranded nucleic acid structures that comprise a nascent RNA hybridized with the DNA template strand, leaving a non-template DNA single-stranded. More specifically, R loops form in vivo as G-rich RNA transcripts invade the DNA duplex and anneal to the template strand to generate an RNA:DNA hybrid, leaving the non-template, G-rich DNA strand in a largely single-stranded conformation (Aguilera and Garcia-Muse, Mol Cell 46:115-124, 2012).DNA-RNA hybrids are a natural occurrence within eukaryotic cells, with levels of these hybrids increasing at sites with high transcriptional activity, such as during transcription initiation, repression, and elongation. RNA-DNA hybrids influence genomic instability, and growing evidence points to an important role for R loops in active gene expression regulation (Ginno et al., Mol Cell 45, 814-825, 2012; Sun et al., Science 340: 619-621, 2013; Bhatia et al., Nature 511, 362-365, 2014). Analysis of the occurrence of such structures is therefore of increasing relevance and herein we describe methods for the in vivo and in vitro identification and characterization of R loops in mammalian systems.R loops (DNA:RNA hybrids and the associated single-stranded DNA) have been traditionally associated with threats to genome integrity, making some regions of the genome more prone to DNA-damaging and mutagenic agents. Initially considered to be rare byproducts of transcription, over the last decade accumulating evidence has pointed to a new view in which R loops form more frequently than previously thought. The R loop field has become an increasingly expanded area of research, placing these structures as a major threat to genome stability but also as potential regulators of gene expression. Special interest has arisen as they have also been linked to a variety of diseases, including neurological disorders and cancer, positioning them as potential therapeutic targets [5].

Keywords: Bisulfite sequencing; CpG island; DRIP; In vitro transcription; R loop; RNA-FISH; Vimentin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CpG Islands
  • DNA / chemistry*
  • DNA / genetics*
  • DNA / isolation & purification
  • Immunoprecipitation
  • In Situ Hybridization, Fluorescence
  • In Vitro Techniques
  • Nucleic Acid Conformation*
  • Nucleic Acid Hybridization*
  • RNA / chemistry*
  • RNA / genetics*
  • RNA / isolation & purification
  • Sequence Analysis, DNA
  • Transcription, Genetic

Substances

  • RNA
  • DNA