Evidence map›Paper›PMID 39197037›Full record

ArticleThe Plant cell2024

FERONIA regulates salt tolerance in Arabidopsis by controlling photorespiratory flux.

Wei Jiang, Zhihao Wang, Yali Li, Xin Liu, Yuying Ren, Chao Li, Shengji Luo, Rahul Mohan Singh, Yan Li, Chanhong Kim and 1 more

Abstract read
In one paragraph

Article in The Plant cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Plant cell surface receptors.The Plant journal : for cell and molecular biology · 2026
    Review
  7. Review
  8. Article
  9. Gene family ofFrontiers in plant science · 2026
    Article
  10. Plants (Basel, Switzerland) · 2025
    Article
  11. Review
  12. Peptide Hormone-Mediated Regulation of Plant Development and Environmental Adaptability.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  13. The pan genome analysis ofHorticulture research · 2025
    Article
  14. Review
  15. Genome-wide analysis of the CrRLK1L gene family inFrontiers in plant science · 2025
    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

11 authors.

Wei JiangKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0009-1587-4345
Zhihao WangKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0005-2055-7820
Yali LiKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0000-7259-9591
Xin LiuKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0000-1790-1946
Yuying RenKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0004-9810-6600
Chao LiKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0009-0002-2973-9362
Shengji LuoUniversity of Chinese Academy of Sciences, Beijing 100049, China.ORCID 0000-0002-5551-3247
Rahul Mohan SinghShanghai Center for Plant Stress Biology, Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0000-0001-7776-0532
Yan LiState Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, National Center for Soybean Improvement, Key Laboratory for Biology and Genetic Improvement of Soybeans (General, Ministry of Agriculture), Jiangsu Collaborative Innovation Center for Modern Crop Production, Nanjing Agricultural University, Nanjing 210095, China.ORCID 0000-0002-1627-7763
Chanhong KimShanghai Center for Plant Stress Biology, Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0000-0003-4133-9070
Chunzhao ZhaoKey Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0000-0003-0284-2095

Funding

CPSF GZB20240743Key Laboratory of Plant Design, and the National Key Laboratory of Plant Molecular GeneticsNational Key Research and Development Program of China 2023YFF1002100National Natural Science Foundation of China 32270283 and 32070295Science and Technology Commission of Shanghai Municipality 22ZR1469600
6 · The paper itself

Abstract

Photorespiration is an energetically costly metabolic pathway in plants that responds to environmental stresses. The molecular basis of the regulation of the photorespiratory cycle under stress conditions remains unclear. Here, we discovered that FERONIA (FER) regulates photorespiratory flow under salt stress in Arabidopsis (Arabidopsis thaliana). FER mutation results in hypersensitivity to salt stress, but disruption of ferredoxin-dependent glutamate synthase 1 (GLU1), an enzyme that participates in the photorespiratory pathway by producing glutamate, greatly suppresses fer-4 hypersensitivity to salt stress primarily due to reduced glycine yield. In contrast, disrupting mitochondrial serine hydroxymethyltransferase1 (SHM1), which is supposed to increase glycine levels by hampering the conversion of glycine to serine in the photorespiratory cycle, aggravates fer-4 hypersensitivity to salt stress. Biochemical data show that FER interacts with and phosphorylates SHM1, and this phosphorylation modulates SHM1 stability. Additionally, the production of proline and its intermediate △1-pyrroline-5-carboxylate (P5C), which are both synthesized from glutamate, also contributes to fer-4 hypersensitivity to salt stress. In conclusion, this study elucidates the functional mechanism of FER in regulating salt tolerance by modulating photorespiratory flux, which greatly broadens our understanding of how plants adapt to high salinity.

Indexed as

ArabidopsisArabidopsis ProteinsSalt ToleranceGene Expression Regulation, PlantGlutamatesGlycineGlycine HydroxymethyltransferaseMutationPhosphorylationPhosphotransferasesPhotosynthesisProlineProtein Serine-Threonine KinasesSalt StressArabidopsis ProteinsAt3g51550 protein, ArabidopsisGlutamatesGlycineGlycine HydroxymethyltransferasePhosphotransferasesProlineProtein Serine-Threonine Kinases

Identifiers

PMID39197037
PMCPMC11530776

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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.