Evidence map›Paper›PMID 42526910›Full record

ReviewPhysiologia plantarum

Spatial and Temporal Dynamics of Phenylpropanoid Pathway-Derived Secondary Metabolites Under Abiotic Stress.

Dativa Gosbert Tibesigwa, Haoqin Zhao, Wenhui Zhuang, Zhenxin Ni, Jingjing Li, Wanxin Li, Xinyu Cui, Zihan Fan, Jingru Ren, Qianqian Liu and 3 more

Abstract readReview
In one paragraph

Review in Physiologia plantarum. 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

13 authors.

Dativa Gosbert TibesigwaState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.ORCID https://orcid.org/0009-0005-1940-3250
Haoqin ZhaoState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.ORCID https://orcid.org/0009-0003-7135-3217
Wenhui ZhuangState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Zhenxin NiWangqing Forestry Bureau of Jilin Province, Wangqing, China.
Jingjing LiState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Wanxin LiState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Xinyu CuiState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Zihan FanState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Jingru RenState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Qianqian LiuState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.
Shicheng ZhaoSchool of Pharmacy, Harbin University of Commerce, Harbin, China.ORCID https://orcid.org/0000-0001-8458-0660
Meiou SunLiangshui Experimental Forest Farm, Northeast Forestry University, Harbin, China.ORCID https://orcid.org/0009-0006-1938-1829
Jingli YangState Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, China.ORCID https://orcid.org/0000-0003-0922-5954

Funding

Fundamental Research Funds for the Central Universities 2572025AW29
6 · The paper itself

Abstract

Plants, being sessile organisms, depend on finely tuned biochemical mechanisms to cope with environmental challenges. Among these, the phenylpropanoid pathway plays a central role in the production of a diverse array of secondary metabolites. These PAL-derived secondary metabolites accumulate in distinct spatiotemporal patterns across plant organs and adjust dynamically in response to environmental cues. Such spatiotemporal dynamics, regulated by distinct mechanisms, allow plants to maintain physiological function while improving tolerance to abiotic stresses. Recent advances in spatial and temporal omics technologies, such as imaging mass spectrometry (IMS) and spatial transcriptomics (ST), have revolutionized our ability to visualize the localization of secondary metabolites in plant tissues, providing insights into stress resilience. The spatial multi-omics reveals secondary metabolite accumulation and informs on the genes driving their production at each stage of the stress response. High-resolution, advanced computational, and emerging spatial multi-omics frameworks, coupled with machine-learning algorithms for spatial data interpretation, are rapidly enhancing our ability to visualize and model dynamic stress responses. However, significant challenges, including the structural complexity of plant tissues (e.g., rigid cell walls), metabolite diversity, and long life spans, complicate the exploration of secondary metabolite accumulation. Generally, the spatiotemporal accumulation of PAL-derived secondary metabolites under abiotic stress represents a sophisticated adaptive system that optimizes defence, signaling, and growth coordination in plants, aided by regulatory mechanisms such as transcriptional regulation, hormonal signaling, and secondary metabolite transport. This fundamental understanding offers practical insights into plant improvement, enabling targeted engineering and manipulation of phenylpropanoid metabolism to enhance stress tolerance.

Indexed as

PhenylpropionatesPlantsPropanolsSecondary MetabolismStress, PhysiologicalGene Expression Regulation, PlantMultiomicsPhenylpropionatesPropanolsabiotic stressphenylpropanoid pathwaysecondary metabolitesspatiotemporal accumulation

Identifiers

PMID42526910
PMCPMC13421062

What OpenQuestion holds

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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.