Evidence map›Paper›PMID 41571635›Full record

ArticleNature communications2026

The role of low-complexity repeats in RNA-RNA interactions and a deep learning framework for duplex prediction.

Adriano Setti, Giorgio Bini, Flaminia Pellegrini, Valentino Maiorca, Gabriele Proietti, Dimitrios-Miltiadis Vrachnos, Angelo D'Angelo, Alexandros Armaos, Julie Martone, Michele Monti and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. TDP-43 dysfunction induces cryptic circular RNAs in ALS/FTD.bioRxiv : the preprint server for biology · 2026
    Article
  2. 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

15 authors.

Adriano Setti *Department of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0002-4995-2403
Giorgio Bini *Center for Human Technologies (CHT), Fondazione Istituto Italiano Di Tecnologia (IIT), Genoa, Italy.
Flaminia PellegriniDepartment of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.
Valentino MaiorcaDepartment of Computer Science, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0001-5795-3695
Gabriele ProiettiCenter for Human Technologies (CHT), Fondazione Istituto Italiano Di Tecnologia (IIT), Genoa, Italy.
Dimitrios-Miltiadis VrachnosDepartment of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.
Angelo D'AngeloDepartment of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0009-0007-1333-202X
Alexandros ArmaosCenter for Human Technologies (CHT), Fondazione Istituto Italiano Di Tecnologia (IIT), Genoa, Italy.
Julie MartoneInstitute of Molecular Biology and Pathology, CNR, Rome, Italy.
Michele MontiCenter for Human Technologies (CHT), Fondazione Istituto Italiano Di Tecnologia (IIT), Genoa, Italy.
Giancarlo RuoccoCenter for Life Nano- & Neuro-Science, Fondazione Istituto Italiano Di Tecnologia (IIT), Rome, Italy.
Emanuele RodolàDepartment of Computer Science, Sapienza University of Rome, Rome, Italy.
Irene BozzoniDepartment of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0002-3485-8537
Alessio ColantoniDepartmental Faculty of Medicine, UniCamillus-Saint Camillus International University of Health Sciences, Rome, Italy. alessio.colantoni@unicamillus.org.ORCID http://orcid.org/0000-0001-7402-0176
Gian Gaetano TartagliaCenter for Human Technologies (CHT), Fondazione Istituto Italiano Di Tecnologia (IIT), Genoa, Italy. gian.tartaglia@iit.it.ORCID http://orcid.org/0000-0001-7524-6310

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 855923
6 · The paper itself

Abstract

RNA-RNA interactions (RRIs) are fundamental to gene regulation and RNA processing, yet their molecular determinants remain unclear. In this work, we analyze several large-scale RRI datasets and identify low-complexity repeats (LCRs), including simple tandem repeats, as key drivers of RRIs. Our findings reveal that LCRs enable thermodynamically stable interactions with multiple partners, positioning them as key hubs in RNA-RNA interaction networks. These RRIs appear to be important for several aspects of RNA metabolism. Sequencing-based analysis of the lncRNA Lhx1os interactors validates the importance of LCRs in shaping contacts potentially involved in neuronal development. Recognizing the pivotal role of sequence determinants, we develop RIME, a deep learning model that predicts RRIs by leveraging embeddings from a nucleic acid language model. RIME outperforms traditional thermodynamics-based tools, successfully captures the role of LCRs and prioritizes high-confidence interactions, including those established by lncRNAs. RIME is freely available at https://tools.tartaglialab.com/rna_rna .

Indexed as

Deep LearningRNAHumansRNA, Long NoncodingThermodynamicsRNARNA, Long Noncoding

Identifiers

PMID41571635
PMCPMC12905285

What OpenQuestion holds

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Registered trials

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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.