| Literature DB >> 35704209 |
Wei Xu1,2,3, Kuan Li1,2, Qin Li1,2, Shuai Li1,2, Jincong Zhou1,2, Qianwen Sun4,5.
Abstract
R-loop is a three-stranded chromatin structure, comprising one single-stranded DNA and another DNA:RNA hybrid strand, plays various and essential biological functions in many organisms. Developing a precise, efficient, faithful, and unbiased genome-wide R-loop detection method with extensive adaptability in all organisms is at the top priority for R-loop biology. Here, we provide a straightforward and highly efficient protocol for genome-wide strand-specific R-loop profiling in various organisms. In brief, genomic DNA is extracted and fragmented by the cocktail of restriction enzymes, and then the DNA:RNA hybrids are immunoprecipitated, following by the single-stranded DNA adaptor ligation and next-generation sequencing (named as ssDRIP-seq). Coupling with a straightforward and step-by-step bioinformatic pipeline, this method can provide high resolution and comprehensive strand-specific information for R-loop formation. ssDRIP-seq has been successfully applied for detecting R-loops from prokaryotes such as E. coli, to eukaryotes such as S. cerevisiae, mammalian cell culture and tissues, as well as plants Arabidopsis and rice, with high reproducibility and sensitivity.Entities:
Keywords: Genome; Next-generation sequencing; Noncoding RNA; Nucleic acid; R-loop
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Year: 2022 PMID: 35704209 DOI: 10.1007/978-1-0716-2477-7_29
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745