Evidence map›Paper›PMID 42357239›Full record

ReviewPlants (Basel, Switzerland)2026

Intermolecular-Interaction-Driven Adaptive Remodeling: A Network Perspective on Plant Abiotic Stress Responses.

Leidi Liu, Xiangfei Cheng, Yihua Xu, Lu Liu, Shuai Zhong, Xiaohua Chao, Yumin Chen, Chengde Yu, Chengming Fan, Changsong Zou

Abstract readReview
In one paragraph

Review in Plants (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Leidi LiuCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.ORCID 0009-0001-7548-210X
Xiangfei ChengCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Yihua XuCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Lu LiuCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Shuai ZhongCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Xiaohua ChaoCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Yumin ChenCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Chengde YuCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.
Chengming FanState Key Laboratory of Seed Innovation, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0002-1352-8301
Changsong ZouCenter for Molecular Interactions and Translational Applications, School of Life Sciences, Henan University, Kaifeng 475004, China.ORCID 0000-0001-6805-3545

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abiotic stresses, including drought, salinity, alkalinity, temperature extremes, flooding, heavy metals, and emerging pollutants, challenge plant growth and productivity by disturbing water relations, ion balance, redox homeostasis, membrane stability, energy metabolism, and developmental progression. Although substantial progress has been made in the identification of stress-responsive hormones, second messengers, kinases, transcription factors, transporters, and metabolic regulators, plant stress adaptation cannot be fully explained by linear signaling cascades or single tolerance genes. A major unresolved question is how early molecular events are reorganized into coordinated physiological and developmental outputs that support survival, recovery, and productivity. In this review, we propose an intermolecular interaction-driven adaptive remodeling framework for plant abiotic stress responses. This framework emphasizes that stress tolerance emerges from dynamic changes in receptor-ligand recognition, protein-protein interactions, calcium decoding, redox-sensitive modification, phosphorylation networks, transcriptional regulation, chromatin-associated control, and metabolite-mediated feedback. We further emphasize ROS as integrative redox switches that connect stress sensing, defense activation, senescence-related transitions, and recovery, and chromatin-associated mechanisms as regulators that may stabilize primed or memory-like adaptive states. We discuss how these interaction networks converge on core signaling hubs, including abscisic acid, reactive oxygen species, Ca

Indexed as

abiotic stressabscisic acidadaptive remodelingcalcium signalingchromatin regulationcrop resiliencephosphorylationreactive oxygen speciesredox switchstress memory

Identifiers

PMID42357239
PMCPMC13306242

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.