Evidence map›Paper›PMID 41862793›Full record

ArticleBMC genomics2026

Genome-wide identification and functional characterization of MAPKK gene family in Zanthoxylum armatum DC. reveal its potential role in ecological adaptive evolution.

Chongyu Liu, Li Tan, Ruxin Xu, Long Tong, Xia Liu, Jiajia Tang, Chong Sun, Yifei Deng, Mi Kuang, Xia Gong and 3 more

Abstract read
In one paragraph

Article in BMC genomics, 2026. 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

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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. 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

13 authors.

Chongyu Liu *Chongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Li Tan *Chongqing Key Laboratory of Forest Ecological Restoration and Utilization in the Three Gorges Reservoir Area, Chongqing Academy of Forestry Sciences, Chongqing, 400036, China.
Ruxin Xu *Chongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Long TongChongqing Key Laboratory of Forest Ecological Restoration and Utilization in the Three Gorges Reservoir Area, Chongqing Academy of Forestry Sciences, Chongqing, 400036, China.
Xia LiuChongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China. liuxiavip8@163.com.
Jiajia TangChongqing Key Laboratory of Forest Ecological Restoration and Utilization in the Three Gorges Reservoir Area, Chongqing Academy of Forestry Sciences, Chongqing, 400036, China.
Chong SunChongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Yifei DengChongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China.
Mi KuangChongqing Agricultural Technology Promotion General Station, Chongqing, 401120, China.
Xia GongSichuan Province Institute of Agricultural Special Plants, Neijiang, 641200, China.
Lingling PengChongqing Agricultural Technology Promotion General Station, Chongqing, 401120, China.
Dalan FengChongqing Key Laboratory of Forest Ecological Restoration and Utilization in the Three Gorges Reservoir Area, Chongqing Academy of Forestry Sciences, Chongqing, 400036, China.
Zexiong ChenChongqing Key Laboratory of Economic Plant Biotechnology/Collaborative Innovation Center of Special Plant Industry in Chongqing/College of Smart Agriculture, Chongqing University of Arts and Sciences, Chongqing, 402160, China. chenzexiong1979@163.com.

Funding

Chongqing Forestry Science Research Institute Project YLXMXL2506Chongqing Key Laboratory of Forest Ecological Restoration and Utilization in the Three Gorges Reservoir Area zdsys2025-3; zdsys2025-4;Graduate Research Innovation Project of Chongqing University of Arts and Sciences CYS25874National Natural Science Foundation of China 31901324Projects for Innovative Research Groups of Chongqing Universities CXQT21028Scientific Research Projects of Chongqing Science and Technology Bureau CSTB2024NSCQ-MSX0353Special Project for Performance Incentive Guidance in Research Institutions in Chongqing CSTB2023JXJL-YFX0096
6 · The paper itself

Abstract

backgroundZanthoxylum armatum is a vital economic crop in China, but its cultivation is challenged by abiotic stresses like drought and cold. Mitogen-activated protein kinase kinases (MAPKKs) are central signaling components regulating plant stress responses. However, the MAPKK gene family in Z. armatum remained uncharacterized. This study aimed to identify ZaMAPKK genes and elucidate their roles in stress adaptation. Understanding ZaMAPKK functions provides critical genetic targets for molecular breeding programs aimed at developing stress-tolerant cultivars, ensuring sustainable Z. armatum production in marginal environments.

resultsThis study identified 14 MAPKK family members in Z. armatum (ZaMAPKK1-14) via genome-wide analysis. Bioinformatics and experimental analyses revealed that ZaMAPKKs were unstable hydrophilic proteins, predominantly localized in the nucleus. Phylogenetic analysis divided them into four subfamilies (A, B, C, and D), showing high homology with dicotyledonous plants such as Arabidopsis thaliana and soybean. Gene structure analysis indicated significant differences in intron numbers among subfamily members, suggesting functional differentiation. Promoter cis-element analysis identified abundant elements related to light response, hormone regulation, and stress in all genes. Transcriptome and reverse transcription-quantitative PCR (RT-qPCR) analyses revealed that ZaMAPKK7 and ZaMAPKK11 exhibited significantly higher expression across samples from different latitudes, implicating them in regulating Z. armatum stress resistance via activation of stress response pathways. Gene co-expression network analysis indicated that ZaMAPKK genes cooperate with various transcription factors to regulate stress response, light signaling, growth, and metabolism in Z. armatum.

conclusionsThis study identifies ZaMAPKK7 and ZaMAPKK11 as key regulators of stress resistance in Z. armatum. Future work will integrate RT-qPCR and co-expression analyses to validate their functions within the MAPKK cascade and explore synergistic mechanisms with other gene families. Unraveling this regulatory network will accelerate the breeding of stress-tolerant cultivars, ultimately enhancing Zanthoxylum productivity and industrial sustainability.

Indexed as

Adaptation, PhysiologicalMitogen-Activated Protein Kinase KinasesMultigene FamilyPlant ProteinsZanthoxylumEvolution, MolecularGene Expression ProfilingGene Expression Regulation, PlantGenome, PlantGenome-Wide Association StudyPhylogenyPromoter Regions, GeneticStress, PhysiologicalMitogen-Activated Protein Kinase KinasesPlant ProteinsGene co-expressionMAPKKTranscriptomeZanthoxylum armatum

Identifiers

PMID41862793
PMCPMC13126955

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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.