Evidence map›Paper›PMID 42218123›Full record

ArticleNature communications2026

Tunable gene control via RNA splicing with a clinically approved small molecule.

Mateusz Mendel, Dominic Schwarz, Tao Sun, Sophia Tan, Asia Franceschetti, Daria Majcher, Simone Lang, Dario Venetz, Hasane Ratni, Ravi Jagasia and 3 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 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. 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

13 authors.

Mateusz MendelTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland. mateusz.mendel@roche.com.ORCID http://orcid.org/0009-0008-2592-1881
Dominic SchwarzOncology Discovery, Pharma Research and Early Development (pRED), Roche Innovation Center Zurich, Schlieren, Switzerland.ORCID http://orcid.org/0000-0002-0322-5059
Tao SunCell Therapy, Genentech Inc., South San Francisco, CA, USA.
Sophia TanBiochemical and Cellular Pharmacology, Genentech Inc., South San Francisco, CA, USA.
Asia FranceschettiTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Daria MajcherTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Simone LangOncology Discovery, Pharma Research and Early Development (pRED), Roche Innovation Center Zurich, Schlieren, Switzerland.
Dario VenetzOncology Discovery, Pharma Research and Early Development (pRED), Roche Innovation Center Zurich, Schlieren, Switzerland.
Hasane RatniTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID http://orcid.org/0000-0002-8151-8295
Ravi JagasiaNeuroscience and Rare Diseases, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Martin EbelingPredictive Modelling and Data Analysis, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID http://orcid.org/0000-0002-0361-4636
Filip RoudnickyTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7156-2383
Lina SchukurTherapeutic Modalities, Pharma Research and Early Development (pRED), F. Hoffmann-La Roche Ltd, Basel, Switzerland. lina.schukur@roche.com.ORCID http://orcid.org/0009-0009-8150-9928

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise transgene regulation is crucial for safe and effective gene and cell therapies. Current inducible systems often rely on immunogenic exogenous proteins or non-clinically approved inducers, hindering clinical translation. Here we present RisdiON, a compact inducible system controlled by risdiplam, a clinically approved oral drug that acts via splicing modulation. RisdiON utilizes risdiplam-responsive sequences for precise transgene control via endogenous splicing machinery, bypassing exogenous protein regulators, while its split-ATG architecture ensures the expression of native, tag-free proteins. This approach provides robust, dose-dependent induction with minimal leakiness. We demonstrate that RisdiON controls various transgenes in immortalized cell lines and hiPSCs, enables inducible CAR expression in primary T cells, and regulates Cas9 for precise gene editing. Additionally, we achieve reversible transgene expression in vivo using adeno-associated virus (AAV) delivery. The platform is modular and functional across diverse promoters, offering a safe, titratable, and reversible tool when coupled with an orally bioavailable drug to advance next-generation therapies.

Indexed as

Gene Expression RegulationRNA SplicingAnimalsDependovirusGene EditingHumansMiceT-LymphocytesTransgenes

Identifiers

PMID42218123
PMCPMC13392007

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.