Evidence map›Paper›PMID 35666183›Full record

ArticleG3 (Bethesda, Md.)2022

Integrative analysis and prediction of human R-loop binding proteins.

Arun Kumar, Louis-Alexandre Fournier, Peter C Stirling

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% of its field
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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. NAT10-dependent NCell reports · 2026
    Article
  2. Review
  3. Article
  4. Chromosomal R-loops: who R they?Biologia futura · 2024
    Review
  5. Article
  6. Review
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

3 authors at 1 institution in 1 country.

Arun KumarTerry Fox Laboratory, BC Cancer, Vancouver, BC V5Z1L3, Canada.ORCID 0000-0002-5676-7521
Louis-Alexandre FournierTerry Fox Laboratory, BC Cancer, Vancouver, BC V5Z1L3, Canada.ORCID 0000-0002-4649-1197
Peter C StirlingTerry Fox Laboratory, BC Cancer, Vancouver, BC V5Z1L3, Canada.ORCID 0000-0003-2651-4539
University of British Columbia · CA

Funding

CIHR 398871
6 · The paper itself

Abstract

In the past decade, there has been a growing appreciation for R-loop structures as important regulators of the epigenome, telomere maintenance, DNA repair, and replication. Given these numerous functions, dozens, or potentially hundreds, of proteins could serve as direct or indirect regulators of R-loop writing, reading, and erasing. In order to understand common properties shared amongst potential R-loop binding proteins, we mined published proteomic studies and distilled 10 features that were enriched in R-loop binding proteins compared with the rest of the proteome. Applying an easy-ensemble machine learning approach, we used these R-loop binding protein-specific features along with their amino acid composition to create random forest classifiers that predict the likelihood of a protein to bind to R-loops. Known R-loop regulating pathways such as splicing, DNA damage repair and chromatin remodeling are highly enriched in our datasets, and we validate 2 new R-loop binding proteins LIG1 and FXR1 in human cells. Together these datasets provide a reference to pursue analyses of novel R-loop regulatory proteins.

Indexed as

Carrier ProteinsR-Loop StructuresDNA RepairHumansProteomicsRNA-Binding ProteinsTranscription FactorsCarrier ProteinsFXR1 protein, humanRNA-Binding ProteinsTranscription Factorsrandom forestR-loop binding proteinsR-loops

Identifiers

PMID35666183
PMCPMC9339281
OpenAlexW4281873413

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.