Evidence map›Paper›PMID 42171007›Full record

ArticleThe New phytologist2026

Context matters: coordinated transcriptional regulation and root plasticity under multinutrient conditions.

Martin Lyčka, Yu-Chen Liu, Chih-Wei Lin, Jane Shih-Jhen Wang, Hao-Hsuan Kao, Lukáš Fojt, Ting-Ying Wu, Chia-Yi Cheng

Abstract read
In one paragraph

Article in The New phytologist, 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

8 authors.

Martin Lyčka *Department of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0000-0001-9174-4862
Yu-Chen Liu *Department of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0009-0004-4207-1760
Chih-Wei Lin *Department of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0009-0007-2621-3492
Jane Shih-Jhen WangDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0009-0005-1991-0666
Hao-Hsuan KaoDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0009-0004-6964-9462
Lukáš FojtInstitute of Biophysics of the Czech Academy of Sciences, 612 00, Brno, Czech Republic.ORCID https://orcid.org/0000-0002-3686-8536
Ting-Ying WuInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, 10617, Taiwan.ORCID https://orcid.org/0000-0001-6488-5133
Chia-Yi ChengDepartment of Life Science, National Taiwan University, Taipei, 10617, Taiwan.ORCID https://orcid.org/0000-0001-5054-5525

Funding

Academia Sinica AS-SS-112-04-5National Science and Technology Council 112-2813-C-002-139-BNational Science and Technology Council 113-2813-C-002-085-BNational Science and Technology Council 114-2811-B-002-006National Science and Technology Council 114-2811-B-002-112National Science and Technology Council NSTC 112-2313-B-002-018-MY3
6 · The paper itself

Abstract

Plants often encounter simultaneous imbalances in multiple nutrients, but the regulatory logic coordinating their responses remains poorly understood. We aimed to uncover shared transcriptional programs and regulatory nodes underpinning multinutrient adaptation in Arabidopsis thaliana roots. We analyzed publicly available RNA-seq datasets spanning 15 nutrient and beneficial element conditions using differential expression, co-expression network (WGCNA), and gene regulatory network analysis. Selected transcription factors (TFs) were validated via root phenotyping, suberin staining, and ionomic profiling under two-nutrient stress conditions. We identified a core set of 2050 genes responsive to multiple nutrient treatments, enriched for suberin biosynthesis, and structured into modular co-expression clusters. Eight prioritized candidate TFs (ARR10, GBF3, HHO5, NAC32, NF-YA3, NF-YB2, SARD1, and WRKY33) were shown to modulate root system architecture under specific nutrient combinations. WRKY33 and NF-YB2, in particular, regulated nutrient-responsive suberin deposition and ionomic plasticity. These findings reveal suberin remodeling as a shared downstream process in multinutrient responses and suggest that plasticity is not a fixed trait but a modular, polygenic, and context-dependent outcome. Repurposed TFs with pleiotropic functions coordinate structural and physiological traits, providing regulatory entry points for improving nutrient resilience.

Indexed as

ArabidopsisGene Expression Regulation, PlantNutrientsPlant RootsTranscription, GeneticArabidopsis ProteinsGene Regulatory NetworksGenes, PlantLipidsPhenotypeStress, PhysiologicalTranscription FactorsArabidopsis ProteinsLipidssuberinTranscription FactorsArabidopsis thalianacombinatorial nutrient stresscontext‐dependent responsegene regulatory networkplasticityroot system architecturesuberin

Identifiers

PMID42171007
PMCPMC13539951

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.