Evidence map›Paper›PMID 40457200›Full record

ArticleBMC plant biology2025

Cloning and assessment of cold resistance in the transcription factor PhIPT5 from Populus hopeiensis.

Qi Zhang, Tiantian Bi, Ning Wang, Jinling Dai, Yue Bai

Abstract read
In one paragraph

Article in BMC plant biology, 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
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qi ZhangInner Mongolia Agricultural University, Hohhot, China.
Tiantian BiInner Mongolia Agricultural University, Hohhot, China.
Ning WangForestry and Grassland Bureau of Zhuozi County, Ulanqab City, Inner Mongolia, China.
Jinling DaiInner Mongolia Agricultural University, Hohhot, China.
Yue BaiInner Mongolia Agricultural University, Hohhot, China. baiyue@imau.edu.cn.

Funding

National Major Science and Technology Projects of China 2018ZX08020002-005-005
6 · The paper itself

Abstract

backgroundPopulus hopeiensis, a significant afforestation species, faces substantial growth constraints due to cold stress. The IPT gene, a pivotal rate-limiting enzyme in cytokinin synthesis, plays a crucial role in controlling plant reactions to both biotic and abiotic pressures. In this study, we isolated the PhIPT5 gene from Populus hopeiensis and analyzed its biological characteristics and cold tolerance with the aim of providing guidance for the production of cold-resistant poplars.

resultsThe coding sequence (CDS) of the PhIPT5 gene spans 981 bp, encoding 333 amino acid residues with a molecular weight of 37.07 kDa. The PhIPT5 protein has alkaline stability and hydrophilicity. Phylogenetic analysis revealed that Populus hopeiensis IPT5 is closely related to Populus alba. Subcellular localization studies revealed the chloroplastic localization of PhIPT5. We constructed an overexpression vector for PhIPT5 and transformed it into Populus hopeiensis, resulting in improved cold tolerance in transgenic seedlings. Analysis of cytokinin metabolites revealed significantly greater levels in leaves harboring the PhIPT5 gene than in those harboring the CK gene even after exposure to cold. Furthermore, our findings suggest that the PhIPT5 gene primarily regulates the isoamyl pyrophosphate cytokinin metabolism pathway, leading to the synthesis of tZ, iP, and DZ cytokinins.

conclusionOur isolation of PhIPT5 from Populus hopeiensis demonstrated that its overexpression enhances resistance to cold stress in transgenic plants. This work provides a foundation for further elucidating the function of IPT genes and has significant implications for advancing research on enhancing cold tolerance in Populus hopeiensis.

Indexed as

Plant ProteinsPopulusTranscription FactorsAmino Acid SequenceCloning, MolecularCold TemperatureCytokininsGene Expression Regulation, PlantPhylogenyPlants, Genetically ModifiedCytokininsPlant ProteinsTranscription FactorsCold stressCytokininPhIPT5Populus hopeiensis

Identifiers

PMID40457200
PMCPMC12128305

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