Evidence map›Paper›PMID 41717106›Full record

ArticleFrontiers in plant science2026

Morphological, physiological, and transcriptomic analysis of

Yunpeng Gao, Hongling Wang, Shizheng Shi, Ruifang Huang, Liwen Liang, Jue Zhang, Kaipeng Jiang, Tao Huang, Shuxian Li, Cong Lei and 2 more

Abstract read
In one paragraph

Article in Frontiers in plant science, 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

12 authors.

Yunpeng GaoInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Hongling WangInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Shizheng ShiInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Ruifang HuangInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Liwen LiangInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Jue ZhangInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Kaipeng JiangInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.
Tao HuangCollege of Forestry and Grass, Nanjing Forestry University, Nanjing, Jiangsu, China.
Shuxian LiCollege of Forestry and Grass, Nanjing Forestry University, Nanjing, Jiangsu, China.
Cong LeiCollege of Forestry and Grass, Nanjing Forestry University, Nanjing, Jiangsu, China.
Yawen DaiCollege of Forestry and Grass, Nanjing Forestry University, Nanjing, Jiangsu, China.
Dezong SuiInstitute of Genetic Breeding, Jiangsu Academy of Forestry, Nanjing, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Soil salinity is a pressing global issue that undermines agricultural productivity, driving the search for salt-tolerant species and their adaptive strategies. Methods: In this study, we explored the physiological and transcriptomic adaptations of Results and discussion: Through morphological and biochemical analyses, we identified a salinity threshold of 5 ‰. Beyond this threshold, severe leaf senescence and plant death were observed. In physiological profiling, the malondialdehyde (MDA) and relative conductivity (REL) showed dose-dependent increases. Meanwhile, osmoprotectants like proline (PRO), soluble sugar (SS), and soluble protein (SP), as well as antioxidant enzyme activities including peroxidase (POD), catalase (CAT), and superoxide dismutase (SOD), were elevated. This indicates dynamic responses to osmotic and oxidative stress. Transcriptome sequencing revealed 3,858 differentially expressed genes (DEGs). GO and KEGG analyses showed that the commonly up-regulated genes were enriched in 'oxidoreductase activity' (GO:0016491) and 'phenylpropanoid biosynthesis' (ko00940), whereas down-regulated genes were enriched in 'cell-wall organization' (GO:0071554). Among the 421 differentially expressed transcription factors, ERF, WRKY and NAC families constituted 62% of the total, indicating their central role in the salt response. With Weighted Gene Co-expression Network Analysis (WGCNA), we first linked gene modules to physiological traits and found that the MEbrown (r = 0.67-0.99) positively and MEblue (r = -0.69 to -0.98) negatively drives osmoprotectant/antioxidant activation. From these modules, 12 hub genes -especially

Indexed as

antioxidant enzymeosmoprotectantssalt stressTaxodium mucronatumWGCNA

Identifiers

PMID41717106
PMCPMC12913384

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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.