Evidence map›Paper›PMID 34842779›Full record

ArticleNon-coding RNA2021

Progress toward SHAPE Constrained Computational Prediction of Tertiary Interactions in RNA Structure.

Grégoire De Bisschop, Delphine Allouche, Elisa Frezza, Benoît Masquida, Yann Ponty, Sebastian Will, Bruno Sargueil

Open access · goldAbstract read
In one paragraph

Article in Non-coding RNA, 2021. 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
0.6field-weighted citation impact, top 32% 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, 13 citations in OpenAlex.

  1. Article
  2. Fluorescent Dyes for Differential Scanning Fluorimetry of RNA.Chembiochem : a European journal of chemical biology · 2025
    Article
  3. Article
  4. SHAPE Probing to Screen Computationally Designed RNA.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Article
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 1 institution in 2 countries.

Grégoire De BisschopUniversité de Paris, CNRS, UMR 8038/CiTCoM, F-75006 Paris, France.ORCID 0000-0001-9032-9325
Delphine AlloucheUniversité de Paris, CNRS, UMR 8038/CiTCoM, F-75006 Paris, France.ORCID 0000-0002-2436-8083
Elisa FrezzaUniversité de Paris, CNRS, UMR 8038/CiTCoM, F-75006 Paris, France.ORCID 0000-0003-0122-7859
Benoît MasquidaUniversité de Strasbourg, CNRS UMR7156 GMGM, 67084 Strasbourg, France.
Yann PontyEcole Polytechnique, CNRS UMR 7161, LIX, 91120 Palaiseau, France.
Sebastian WillEcole Polytechnique, CNRS UMR 7161, LIX, 91120 Palaiseau, France.
Bruno SargueilUniversité de Paris, CNRS, UMR 8038/CiTCoM, F-75006 Paris, France.
Centre National de la Recherche Scientifique · FR

Funding

Agence Nationale de la Recherche ANR-19-CE30-0021-03Agence Nationale de la Recherche ANR-19-CE45-0023-02Fondation pour la Recherche Médicale DBI20141231337
6 · The paper itself

Abstract

As more sequencing data accumulate and novel puzzling genetic regulations are discovered, the need for accurate automated modeling of RNA structure increases. RNA structure modeling from chemical probing experiments has made tremendous progress, however accurately predicting large RNA structures is still challenging for several reasons: RNA are inherently flexible and often adopt many energetically similar structures, which are not reliably distinguished by the available, incomplete thermodynamic model. Moreover, computationally, the problem is aggravated by the relevance of pseudoknots and non-canonical base pairs, which are hardly predicted efficiently. To identify nucleotides involved in pseudoknots and non-canonical interactions, we scrutinized the SHAPE reactivity of each nucleotide of the 188 nt long lariat-capping ribozyme under multiple conditions. Reactivities analyzed in the light of the X-ray structure were shown to report accurately the nucleotide status. Those that seemed paradoxical were rationalized by the nucleotide behavior along molecular dynamic simulations. We show that valuable information on intricate interactions can be deduced from probing with different reagents, and in the presence or absence of Mg

Indexed as

ribozymeRNA structure modelingshape probing

Identifiers

PMID34842779
PMCPMC8628965
OpenAlexW3213669638

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.