Evidence map›Paper›PMID 41046299›Full record

ArticlePlant cell reports2025

GmAP2 enhances plant tolerance to aluminum toxicity and phosphorus deficiency in Arabidopsis.

Cheng Li, Pengxin Du, Lidan Wang, Xin Xu, Hongying Zhong, Yanbo Cheng, Tengxiang Lian, Lu Li, Qibin Ma

Abstract read
In one paragraph

Article in Plant cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Cheng Li *Guangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Pengxin Du *Guangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Lidan WangGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Xin XuGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Hongying ZhongGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Yanbo ChengGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Tengxiang LianGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Lu LiCollege of Life Sciences, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China. lilu@scau.edu.cn.
Qibin MaGuangdong Subcenter of the National Center for Soybean Improvement, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China. maqibin@scau.edu.cn.ORCID http://orcid.org/0000-0003-3331-3399

Funding

the National Natural Science Foundation of China 31771816the National Natural Science Foundation of China 31971965the National Natural Science Foundation of China 32472073the Seed Industry Revitalization Project for Provincial Rural Revitalization Strategy in 2024 2024-NPY-00-017the STI 2030-Major Project 2023ZD04072
6 · The paper itself

Abstract

key messageOverexpression of the GmAP2 gene regulates several aspects of gene expression in Arabidopsis, including acid-aluminum stress, low-phosphorus stress, ERF family transcription factors, ABA signaling, and genes related to lateral root development. The overexpression of GmAP2 can help plants mitigate the effects of aluminum toxicity and increase their tolerance to low-phosphorus stress. Ethylene response factors (ERFs) represent one of the largest transcription factor families in plants and are involved in regulating biotic and abiotic stresses, as well as growth and development in higher plants. In this study, the soybean GmAP2 gene, encoding the AP2/ERF transcription factor, is a downstream gene of GsMYB7, which enhances soybean tolerance to aluminum toxicity under acidic conditions, referred to as acid-aluminum stress. The expression pattern of GmAP2, which is constitutive and rich in roots, was upregulated under acid-aluminum and low-phosphorus stress. The resistance phenotypes of the wild-type and GmAP2-overexpressing lines were investigated by treatment with acid-aluminum plates and low-phosphorus plates, respectively. The results revealed significant differences between the GmAP2 transgenic lines and the wild type, and compared with the wild-type plants, the genetically modified plants presented significantly better physiological indicators, such as fresh weight, root length, and number of lateral roots. Under acid-aluminum stress, changes in weight, MDA content, and proline content in Arabidopsis thaliana were evaluated. The genes associated with these pathways, including genes related to the acid-aluminum response (AtALMT, AtALS3, AtSTOP1, and AtMATE), ERF family (AtERF6, AtERF15, AtERF5, and AtERF109), and/or ABA response (AtABI5, AtRD29A, AtRAP2.6, AtABI1, and AtABI2), are significantly regulated. In the context of low-phosphorus stress, a comprehensive analysis of the regulatory landscape revealed significant alterations in genes involved in these pathways, including low phosphorus-responsive genes (AtPHT1; 1, AtPHO1, AtPHR1, and AtMGD2), ERF family genes (AtERF1, AtERF6, AtERF13, and AtERF109), and/or genes associated with lateral root development (AtKCS16). These regulatory changes occurred in response to low-phosphorus stress. These results provide a basis for breeding soybean varieties that can increase their tolerance to the stresses of aluminum toxicity and low phosphorus.

Indexed as

AluminumArabidopsisPhosphorusPlant ProteinsArabidopsis ProteinsGene Expression Regulation, PlantGlycine maxPlant RootsPlants, Genetically ModifiedStress, PhysiologicalTranscription FactorsAluminumArabidopsis ProteinsPhosphorusPlant ProteinsTranscription FactorsAcid-aluminumArabidopsisGmAP2Low phosphorusSoybean

Identifiers

PMID41046299
PMCPMC12496291

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LicenceCC BY-NC-ND
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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.