4.7 Article

Isolation and Characterization of Erianthus arundinaceus Phosphate Transporter 1 (PHT1) Gene Promoter and 5′ Deletion Analysis of Transcriptional Regulation Regions under Phosphate Stress in Transgenic Tobacco

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PLANTS-BASEL
卷 12, 期 21, 页码 -

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MDPI
DOI: 10.3390/plants12213760

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Erianthus arundinaceus; high-affinity phosphate transporter; PHT1;2; promoter analysis; tobacco transgenic; Pi stress

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Phosphorus deficiency has a significant impact on plant growth and development. The use of promoters from phosphate transporter genes can enhance phosphate uptake abilities in genetically modified plants, leading to improved crop yields in phosphate-deficient soils. In this study, the EaPHT1;2 gene from Erianthus arundinaceus was isolated and characterized. The promoter region of EaPHT1;2 showed higher expression than the commonly used CaMV35S promoter. The short promoter sequence of EaPHT1;2 showed significant expression under low-Pi-stress conditions and holds promise for developing stress-tolerant transgenic crops.
Phosphorus deficiency highly interferes with plant growth and development. Plants respond to persistent P deficiency by coordinating the expression of genes involved in the alleviation of stress. Promoters of phosphate transporter genes are a great choice for the development of genetically modified plants with enhanced phosphate uptake abilities, which improve crop yields in phosphate-deficient soils. In our previous study, the sugarcane phosphate transporter PHT1;2 gene showed a significantly high expression under salinity stress. In this study, the Erianthus arundinaceus EaPHT1;2 gene was isolated and characterized using various in silico tools. The deduced 542 amino acid residues have 10 transmembrane domains, with a molecular weight and isoelectric point of 58.9 kDa and 9.80, respectively. They displayed 71-96% similarity with Arabidopsis thaliana, Zea mays, and the Saccharum hybrid. To elucidate the function of the 5 ' regulatory region, the 1.1 kb promoter was isolated and validated in tobacco transgenics under Pi stress. The EaPHT1;2 promoter activity was detected using a beta-glucuronidase (GUS) assay. The EaPHT1;2 promoter showed 3- to 4.2-fold higher expression than the most widely used CaMV35S promoter. The 5 ' deletion analysis with and without 5 ' UTRs revealed a small-sized 374 bp fragment with the highest promoter activity among 5 ' truncated fragments, which was 2.7 and 4.2 times higher than the well-used CaMV35S promoter under normal and Pi deprivation conditions, respectively. The strong and short promoter of EaPHT1;2 with 374 bp showed significant expression in low-Pi-stress conditions and it could be a valuable source for the development of stress-tolerant transgenic crops.

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