Evidence map›Paper›PMID 33863890›Full record

ArticleNature communications2021

Conserved long-range base pairings are associated with pre-mRNA processing of human genes.

Svetlana Kalmykova, Marina Kalinina, Stepan Denisov, Alexey Mironov, Dmitry Skvortsov, Roderic Guigó, Dmitri Pervouchine

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  6. Unveiling Functional Long-Range RNA Structures via RIC-seq Analysis.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  7. Ancestral intronic splicing regulatory elements in the SCNbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
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  13. Identification of RNA structures and their roles in RNA functions.Nature reviews. Molecular cell biology · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. NAR genomics and bioinformatics · 2024
    Article
  19. Article
  20. 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

7 authors at 3 institutions in 2 countries.

Svetlana KalmykovaSkolkovo Institute of Science and Technology, Moscow, Russia.
Marina KalininaSkolkovo Institute of Science and Technology, Moscow, Russia.ORCID http://orcid.org/0000-0001-6325-3054
Stepan DenisovSkolkovo Institute of Science and Technology, Moscow, Russia.
Alexey MironovSkolkovo Institute of Science and Technology, Moscow, Russia.
Dmitry SkvortsovFaculty of Chemistry, Moscow State University, Moscow, Russia.
Roderic GuigóCenter for Genomic Regulation and UPF, Barcelona, Spain.ORCID http://orcid.org/0000-0002-5738-4477
Dmitri PervouchineSkolkovo Institute of Science and Technology, Moscow, Russia. d.pervouchine@skoltech.ru.
Skolkovo Institute of Science and Technology · RUCentre for Genomic Regulation · ESLomonosov Moscow State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of nucleic acids to form double-stranded structures is essential for all living systems on Earth. Current knowledge on functional RNA structures is focused on locally-occurring base pairs. However, crosslinking and proximity ligation experiments demonstrated that long-range RNA structures are highly abundant. Here, we present the most complete to-date catalog of conserved complementary regions (PCCRs) in human protein-coding genes. PCCRs tend to occur within introns, suppress intervening exons, and obstruct cryptic and inactive splice sites. Double-stranded structure of PCCRs is supported by decreased icSHAPE nucleotide accessibility, high abundance of RNA editing sites, and frequent occurrence of forked eCLIP peaks. Introns with PCCRs show a distinct splicing pattern in response to RNAPII slowdown suggesting that splicing is widely affected by co-transcriptional RNA folding. The enrichment of 3'-ends within PCCRs raises the intriguing hypothesis that coupling between RNA folding and splicing could mediate co-transcriptional suppression of premature pre-mRNA cleavage and polyadenylation.

Indexed as

A549 CellsBase PairingBase SequenceConserved SequenceDNA, ComplementaryGene LibraryHep G2 CellsHumansIntronsPolyadenylationRNA FoldingRNA PrecursorsRNA-SeqRNA SplicingDNA, ComplementaryRNA Precursors

Identifiers

PMID33863890
PMCPMC8052449
OpenAlexW3153385703

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.