Evidence map›Paper›PMID 41699382›Full record

ReviewNature reviews. Genetics2026

Bridging technical innovation and computational advances in studies of RNA-protein assemblies.

Luca Ducoli, Suhas Srinivasan, Eimon Amjadi, Paul A Khavari

Abstract readReview
In one paragraph

Review in Nature reviews. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Luca DucoliProgram in Epithelial Biology, Stanford University, Stanford, CA, USA. lducoli@stanford.edu.ORCID http://orcid.org/0000-0003-1731-9029
Suhas SrinivasanProgram in Epithelial Biology, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-8309-9648
Eimon AmjadiProgram in Epithelial Biology, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0009-0007-3149-4874
Paul A KhavariProgram in Epithelial Biology, Stanford University, Stanford, CA, USA. khavari@stanford.edu.ORCID http://orcid.org/0000-0003-0098-4989

Funding

REGULATORS OF EPIDERMAL GENE EXPRESSIONR01AR045192 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1999 to 2026
$9.9M
Signaling Regulators of Epithelial Homeostasis and NeoplasiaR01AR049737 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 2004 to 2026
$7.1M
RNA-Dependent Protein Assemblies in Epidermal HomeostasisK99AR086341 · NIAMS · STANFORD UNIVERSITY · PI Luca Ducoli · 2025 to 2026
$205k
BLRD VA I01 BX001409NIAMS NIH HHS K99 AR086341NIAMS NIH HHS R01 AR045192NIAMS NIH HHS R01 AR049737
6 · The paper itself

Abstract

RNA-dependent protein assemblies - including the spliceosome, ribosome and RNA-dependent membraneless organelles - have crucial roles in diverse cellular processes through RNA scaffolding and hierarchical assembly. Various empirical techniques and artificial intelligence algorithms have been developed to help understand the architecture, dynamics and functional implications of RNA-protein complexes, and their further development is underway to comprehensively integrate this information. This Review explores how combining these diverse technologies will enhance our understanding of the biological functions of RNA-dependent protein assemblies. We first explore methodological frontiers, contrasting traditional approaches with new platforms, which enable the identification and tracking of RNA-protein assembly dynamics on the same RNA molecules. We then present avenues for integrating these new experimental techniques with machine-learning methods to improve both predictive models of RNA-protein assembly and functional RNA design. We discuss how the synergy between experimental and digital biology can drive new insights into disease mechanisms and therapeutic strategies, including targeted modulation of pathogenic RNA-protein assemblies. Finally, we examine roadmaps for future research, emphasizing the potential of closed-loop systems that iteratively refine our understanding of RNA-protein assemblies through cycles of hypothesis generation, prediction, experimentation and validation.

Indexed as

Computational BiologyRNARNA-Binding ProteinsAnimalsHumansMachine LearningRibosomesSpliceosomesRNARNA-Binding Proteins

Identifiers

PMID41699382
PMCPMC13246297

What OpenQuestion holds

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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.