Evidence map›Paper›PMID 40415535›Full record

ArticleThe New phytologist2025

At-RS31 orchestrates hierarchical cross-regulation of splicing factors and integrates alternative splicing with TOR-ABA pathways.

Tino Köster, Peter Venhuizen, Martin Lewinski, Ezequiel Petrillo, Yamile Marquez, Armin Fuchs, Debashish Ray, Barbara A Nimeth, Stefan Riegler, Sophie Franzmeier and 9 more

Abstract read
In one paragraph

Article in The New phytologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. bioRxiv : the preprint server for biology · 2025
    Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Tino Köster *RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, 33615, Germany.ORCID https://orcid.org/0000-0003-3984-9813
Peter Venhuizen *Institute of Molecular Plant Biology, Department of Biotechnology and Food Science, BOKU University, Vienna, 1190, Austria.ORCID https://orcid.org/0000-0003-2835-1833
Martin Lewinski *RNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, 33615, Germany.ORCID https://orcid.org/0000-0002-2692-3319
Ezequiel PetrilloInstituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, 1428, Argentina.ORCID https://orcid.org/0000-0002-0025-3708
Yamile MarquezMax Perutz Labs, Medical University Vienna, Vienna BioCenter (VBC), Vienna, 1030, Austria.ORCID https://orcid.org/0000-0003-1686-5992
Armin FuchsMax Perutz Labs, Medical University Vienna, Vienna BioCenter (VBC), Vienna, 1030, Austria.
Debashish RayDonnelly Centre, University of Toronto, Toronto, ON, M5S 3E1, Canada.ORCID https://orcid.org/0000-0003-2021-1115
Barbara A NimethInstitute of Molecular Plant Biology, Department of Biotechnology and Food Science, BOKU University, Vienna, 1190, Austria.ORCID https://orcid.org/0000-0001-8692-8413
Stefan RieglerInstitute of Molecular Plant Biology, Department of Biotechnology and Food Science, BOKU University, Vienna, 1190, Austria.ORCID https://orcid.org/0000-0003-3413-1343
Sophie FranzmeierInstitute of Molecular Plant Biology, Department of Biotechnology and Food Science, BOKU University, Vienna, 1190, Austria.ORCID https://orcid.org/0000-0002-1265-6790
Florencia S RodríguezInstituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, 1428, Argentina.ORCID https://orcid.org/0009-0000-4369-9876
Federico E AballayInstituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, 1428, Argentina.ORCID https://orcid.org/0009-0007-8533-5748
Rocío S TognaccaInstituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, 1428, Argentina.ORCID https://orcid.org/0000-0001-9678-3676
Hong ZhengDonnelly Centre, University of Toronto, Toronto, ON, M5S 3E1, Canada.
Timothy HughesDonnelly Centre, University of Toronto, Toronto, ON, M5S 3E1, Canada.ORCID https://orcid.org/0000-0002-8721-4719
Quaid MorrisSloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.ORCID https://orcid.org/0000-0002-2760-6999
Andrea BartaMax Perutz Labs, Medical University Vienna, Vienna BioCenter (VBC), Vienna, 1030, Austria.ORCID https://orcid.org/0000-0002-8851-406X
Dorothee StaigerRNA Biology and Molecular Physiology, Faculty of Biology, Bielefeld University, Bielefeld, 33615, Germany.ORCID https://orcid.org/0000-0002-1341-1381
Maria KalynaInstitute of Molecular Plant Biology, Department of Biotechnology and Food Science, BOKU University, Vienna, 1190, Austria.ORCID https://orcid.org/0000-0003-4702-7625

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Post-transcriptional Regulatory NetworksR01HG013328 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI Quaid Morris · 2023 to 2026
$2.6M
Systematic characterization of unconventional RNA binding proteinsR01HG008613 · NHGRI · UNIVERSITY OF TORONTO · PI BLENCOWE, BENJAMIN, GREENBLATT, JACK · 2015 to 2017
$1.0M
Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación, Argentina PICT 2020 02865Austrian Science Fund P26333CIHR PJT-162255Deutsche Forschungsgemeinschaft STA653/16-1International Centre for Genetic Engineering and Biotechnology CRP/ARG22-03NCI NIH HHS P30 CA008748NHGRI NIH HHS R01 HG008613NHGRI NIH HHS R01 HG013328NIH HHS R01 HG008613NIH HHS R01 HG013328
6 · The paper itself

Abstract

Alternative splicing is essential for plants, enabling a single gene to produce multiple transcript variants to boost functional diversity and fine-tune responses to environmental and developmental cues. Arabidopsis thaliana At-RS31, a plant-specific splicing factor in the Serine/Arginine-rich (SR) protein family, responds to light and the Target of Rapamycin (TOR) signalling pathway, yet its downstream targets and regulatory impact remain unknown. To identify At-RS31 targets, we applied individual-nucleotide resolution crosslinking and immunoprecipitation (iCLIP) and RNAcompete assays. Transcriptomic analyses of At-RS31 mutant and overexpressing plants further revealed its effects on alternative splicing. iCLIP identified 4034 At-RS31 binding sites across 1421 genes, enriched in CU-rich and CAGA RNA motifs. Comparative iCLIP and RNAcompete data indicate that the arginine/serine (RS) domain of At-RS31 may influence its binding specificity in planta, underscoring the value of combining in vivo and in vitro approaches. Transcriptomic analysis showed that At-RS31 modulates diverse splicing events, particularly intron retention and exitron splicing, and influences other splicing modulators, acting as a hierarchical regulator. By regulating stress response genes and genes in both TOR and abscisic acid signalling pathways, At-RS31 may help integrate these signals, balancing plant growth with environmental adaptability through alternative splicing.

Indexed as

Abscisic AcidAlternative SplicingArabidopsisArabidopsis ProteinsRNA Splicing FactorsSerine-Arginine Splicing FactorsSignal TransductionTOR Serine-Threonine KinasesGene Expression Regulation, PlantMutationPhosphatidylinositol 3-KinasesProtein BindingAbscisic AcidArabidopsis ProteinsPhosphatidylinositol 3-KinasesRNA Splicing FactorsSerine-Arginine Splicing FactorsTOR protein, ArabidopsisTOR Serine-Threonine KinasesABAalternative splicingArabidopsis thalianabinding siteiCLIPRNAcompeteSR proteinsTOR kinase

Identifiers

PMID40415535
PMCPMC12177302

What OpenQuestion holds

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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.