Evidence map›Paper›PMID 27298336›Full record

ArticleGenes & development2016

S1-DRIP-seq identifies high expression and polyA tracts as major contributors to R-loop formation.

Lamia Wahba, Lorenzo Costantino, Frederick J Tan, Anjali Zimmer, Douglas Koshland

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

190 citing papers in PubMed, 2 syntheses or guidelines pooled it, 286 citations in OpenAlex.

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130 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Lamia WahbaDepartment of Cell and Molecular Biology, University of California at Berkeley, Berkeley, California 94720, USA;
Lorenzo CostantinoDepartment of Cell and Molecular Biology, University of California at Berkeley, Berkeley, California 94720, USA;
Frederick J TanDepartment of Embryology, Carnegie Institution for Science, Baltimore, Maryland 21218, USA.
Anjali ZimmerDepartment of Cell and Molecular Biology, University of California at Berkeley, Berkeley, California 94720, USA;
Douglas KoshlandDepartment of Cell and Molecular Biology, University of California at Berkeley, Berkeley, California 94720, USA;
University of California, Berkeley · USDepartment of Embryology · US

Funding

Elucidating chromosome structure and function through the lens of SMC complexes and R-loopsR35GM118189 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI KOSHLAND, DOUGLAS E · 2016 to 2025
$7.1M
RNA:DNA hybrids and genome instabilityR01GM107583 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI KOSHLAND, DOUGLAS E · 2013 to 2015
$853k
NIGMS NIH HHS R01 GM107583NIGMS NIH HHS R35 GM118189
6 · The paper itself

Abstract

R loops form when transcripts hybridize to homologous DNA on chromosomes, yielding a DNA:RNA hybrid and a displaced DNA single strand. R loops impact the genome of many organisms, regulating chromosome stability, gene expression, and DNA repair. Understanding the parameters dictating R-loop formation in vivo has been hampered by the limited quantitative and spatial resolution of current genomic strategies for mapping R loops. We report a novel whole-genome method, S1-DRIP-seq (S1 nuclease DNA:RNA immunoprecipitation with deep sequencing), for mapping hybrid-prone regions in budding yeast Saccharomyces cerevisiae Using this methodology, we identified ∼800 hybrid-prone regions covering 8% of the genome. Given the pervasive transcription of the yeast genome, this result suggests that R-loop formation is dictated by characteristics of the DNA, RNA, and/or chromatin. We successfully identified two features highly predictive of hybrid formation: high transcription and long homopolymeric dA:dT tracts. These accounted for >60% of the hybrid regions found in the genome. We demonstrated that these two factors play a causal role in hybrid formation by genetic manipulation. Thus, the hybrid map generated by S1-DRIP-seq led to the identification of the first global genomic features causal for R-loop formation in yeast.

Indexed as

Gene ExpressionChromosome MappingDNA, FungalGenome, FungalGenomicsHistonesPoly AProtein ConformationRNA, FungalSaccharomyces cerevisiaeSingle-Strand Specific DNA and RNA EndonucleasesDNA, FungalHistonesPoly ARNA, FungalSingle-Strand Specific DNA and RNA EndonucleasesDNA:RNA hybridspolyA tractsR loopsRNase Htranscription

Identifiers

PMID27298336
PMCPMC4911931
OpenAlexW2423627688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.