Evidence map›Paper›PMID 41689257›Full record

ArticlePlant communications2026

The unconventional G protein AtYchF1 interacts with ribosomal protein AtRPS7 to modulate selective translation for balancing plant growth and stress responses in Arabidopsis.

Sau-Shan Cheng, Jacky Chi-Ki Ngo, Yee-Shan Ku, Zhixia Xiao, Ming-Yan Cheung, Hon-Ming Lam

Abstract read
In one paragraph

Article in Plant 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. 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

6 authors.

Sau-Shan ChengSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China.
Jacky Chi-Ki NgoSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China.
Yee-Shan KuSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China.
Zhixia XiaoSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China.
Ming-Yan CheungSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China. Electronic address: cheungmy@cuhk.edu.hk.
Hon-Ming LamSchool of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China; Centre for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong SAR, China. Electronic address: honming@cuhk.edu.hk.

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

Plants must balance normal growth with stress responses by interpreting environmental signals. This balancing act relies on key regulatory mechanisms, including post-transcriptional regulation, translational control, and protein degradation, which help maintain appropriate cellular protein levels. Here, we investigate the role of the unconventional GTPase YchF1, a known negative regulator of stress responses, in resource allocation in Arabidopsis thaliana. Overexpression of AtYchF1 in the atychf1 mutant background improves growth under nutrient-deficient conditions but increases salt sensitivity, and these phenotypes depend on the interaction between AtYchF1 and the ribosomal protein AtRPS7. Proteomic and translatomic analyses revealed that AtYchF1 inhibits the translation of transcripts containing a CUCU motif in their 3' untranslated regions, a feature prevalent among stress-responsive genes, and that this repression is AtRPS7-binding dependent. By preventing the overproduction of stress-related proteins, AtYchF1 redirects resources toward the production of translation- and photosynthesis-related proteins, particularly under suboptimal nutrient conditions. Our findings establish a novel physiological role for AtYchF1 in restraining stress protein production in the absence of abiotic or biotic stress, thereby enabling plants to thrive, especially in nutrient-deficient environments.

Indexed as

ArabidopsisArabidopsis ProteinsGTP-Binding ProteinsProtein BiosynthesisRibosomal ProteinsGene Expression Regulation, PlantRNA Cap-Binding ProteinsStress, PhysiologicalArabidopsis ProteinsAt2g13540 protein, ArabidopsisGTP-Binding ProteinsRibosomal ProteinsRNA Cap-Binding Proteinsplant stress responseribosomal protein bindingribosomal protein S7RPS7translational regulationunconventional GTPaseYchF1

Identifiers

PMID41689257
PMCPMC13370236

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.