Defining the location of promoter-associated R-loops at near-nucleotide resolution using bisDRIP-seq.

Abstract:

:R-loops are features of chromatin consisting of a strand of DNA hybridized to RNA, as well as the expelled complementary DNA strand. R-loops are enriched at promoters where they have recently been shown to have important roles in modifying gene expression. However, the location of promoter-associated R-loops and the genomic domains they perturb to modify gene expression remain unclear. To resolve this issue, we developed a bisulfite-based approach, bisDRIP-seq, to map R-loops across the genome at near-nucleotide resolution in MCF-7 cells. We found the location of promoter-associated R-loops is dependent on the presence of introns. In intron-containing genes, R-loops are bounded between the transcription start site and the first exon-intron junction. In intronless genes, the 3' boundary displays gene-specific heterogeneity. Moreover, intronless genes are often associated with promoter-associated R-loop formation. Together, these studies provide a high-resolution map of R-loops and identify gene structure as a critical determinant of R-loop formation.

journal_name

Elife

journal_title

eLife

authors

Dumelie JG,Jaffrey SR

doi

10.7554/eLife.28306

subject

Has Abstract

pub_date

2017-10-26 00:00:00

issn

2050-084X

pii

28306

journal_volume

6

pub_type

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