Evidence map›Paper›PMID 33846592›Full record

ReviewNature plants2021

Stress-induced reactive oxygen species compartmentalization, perception and signalling.

Bardo Castro, Matteo Citterico, Sachie Kimura, Danielle M Stevens, Michael Wrzaczek, Gitta Coaker

Open access · greenAbstract readReview
In one paragraph

Review in Nature plants, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed
23.4field-weighted citation impact, top 1% of its field
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

175 citing papers in PubMed, 426 citations in OpenAlex.

  1. Chitosan activates a sequential CaPlant signaling & behavior · 2026
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  7. Histone Modification Complex JMJ704-HDA709 Negatively Regulates Salinity Tolerance in Rice.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Article
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  10. Linking redox and calcium signaling via thioredoxins.Journal of experimental botany · 2026
    Review
  11. Review
  12. Review
  13. Combined Mechanisms ofMicroorganisms · 2026
    Article
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  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

115 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 4 countries.

Bardo Castro *Department of Plant Pathology, University of California, Davis, Davis, CA, USA.
Matteo Citterico *Organismal and Evolutionary Biology Research Programme, Viikki Plant Science Centre, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-7585-4401
Sachie Kimura *Ritsumeikan Global Innovation Research Organization, Ritsumeikan University, Kusatsu, Japan.ORCID http://orcid.org/0000-0001-5736-2123
Danielle M StevensDepartment of Plant Pathology, University of California, Davis, Davis, CA, USA.
Michael WrzaczekOrganismal and Evolutionary Biology Research Programme, Viikki Plant Science Centre, University of Helsinki, Helsinki, Finland. michael.wrzaczek@umbr.cas.cz.ORCID http://orcid.org/0000-0002-5946-9060
Gitta CoakerDepartment of Plant Pathology, University of California, Davis, Davis, CA, USA. glcoaker@ucdavis.edu.ORCID http://orcid.org/0000-0003-0899-2449
University of California, Davis · USUniversity of Helsinki · FIRitsumeikan University · JP

Funding

Immune Perception of Bacterial Pathogens in PlantsR35GM136402 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Gitta Laurel Coaker · 2020 to 2026
$3.0M
NIGMS NIH HHS R35 GM136402
6 · The paper itself

Abstract

Reactive oxygen species (ROS) are essential for life and are involved in the regulation of almost all biological processes. ROS production is critical for plant development, response to abiotic stresses and immune responses. Here, we focus on recent discoveries in ROS biology emphasizing abiotic and biotic stress responses. Recent advancements have resulted in the identification of one of the first sensors for extracellular ROS and highlighted waves of ROS production during stress signalling in Arabidopsis. Enzymes that produce ROS, including NADPH oxidases, exhibit precise regulation through diverse post-translational modifications. Discoveries highlight the importance of both amino- and carboxy-terminal regulation of NADPH oxidases through protein phosphorylation and cysteine oxidation. Here, we discuss advancements in ROS compartmentalization, systemic ROS waves, ROS sensing and post-translational modification of ROS-producing enzymes and identify areas where foundational gaps remain.

Indexed as

Signal TransductionStress, PhysiologicalArabidopsisReactive Oxygen SpeciesReactive Oxygen Species

Identifiers

PMID33846592
PMCPMC8751180
OpenAlexW3156600989

What OpenQuestion holds

Textmetadata
LicenceTDM
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.