Zhao Hong, Qiao Guang, Wu Yawei, Shen Luonan, Deng Lin, Wen Xiaopeng
Key laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Institute of Agro-bioengineering/College of Life Sciences, Guizhou University, Guiyang, Guizhou Province, 550025, China.
College of Ecological Engineering, Guizhou University of Engineering Science, Bijie, Guizhou, 551700, China.
BMC Plant Biol. 2025 Jun 4;25(1):758. doi: 10.1186/s12870-025-06577-9.
Phosphorus (Pi) is crucial for the growth and development of plants, and Phosphate transporter 1 (PHT1) genes are key in Pi absorption and signaling. PHT1 and phosphate starvation response 1 (PHR1) form the PHR1-PHT1 module, which is essential for Pi uptake and signaling across various species. However, its role in the apple rootstock has not yet been clear so far.
To gain a clearer insight into the PHR1-PHT1 module's function in coping with low-Pi stress. A transcriptomic analysis of Malus mandshurica, a line with high Pi deficiency tolerance, identified 13 genes of MmPHT1 in response to low-Pi stress. The expression levels of MmPHT1 genes varied in response to low-Pi stress, as shown by qRT-PCR analysis. The analysis of promoter activity revealed that the MmPHT1;5 promoter activated GUS gene expression. The combination of dual-luciferase reporter and yeast one-hybrid (Y1H) assays demonstrated that MmPHR1 interacts with the MmPHT1;5 promoter. Using CRISPR/Cas9 and overexpressing vectors system to transform apple callus to investigate the role of MmPHT1;5 under Pi deficiency. Notably, the OE-MmPHT1;5 line calli showed marked enhancements in acid phosphatase (ACP) activities and total and inorganic Pi contents compared to the wild type. Conversely, the KO-MmPHT1;5 calli showed significant reductions in Pi accumulation, implying it could be involved in the absorption of Pi in apples.
MmPHT1;5 plays a substantial role in enhancing low-Pi stress by facilitating Pi absorption in M. mandshurica.
磷(Pi)对植物的生长发育至关重要,磷酸盐转运蛋白1(PHT1)基因在Pi吸收和信号传导中起关键作用。PHT1和磷饥饿响应1(PHR1)形成了PHR1-PHT1模块,这对于跨物种的Pi吸收和信号传导至关重要。然而,其在苹果砧木中的作用迄今尚不清楚。
为了更清楚地了解PHR1-PHT1模块在应对低Pi胁迫中的功能。对具有高Pi缺乏耐受性的山荆子进行转录组分析,鉴定出13个响应低Pi胁迫的MmPHT1基因。qRT-PCR分析表明,MmPHT1基因的表达水平因低Pi胁迫而有所不同。启动子活性分析表明,MmPHT1;5启动子激活了GUS基因表达。双荧光素酶报告基因和酵母单杂交(Y1H)分析表明,MmPHR1与MmPHT1;5启动子相互作用。利用CRISPR/Cas9和过表达载体系统转化苹果愈伤组织,研究MmPHT1;5在Pi缺乏条件下的作用。值得注意的是,与野生型相比,OE-MmPHT1;5系愈伤组织的酸性磷酸酶(ACP)活性、总磷和无机磷含量均有显著提高。相反,KO-MmPHT1;5愈伤组织的Pi积累显著减少,这意味着它可能参与苹果中Pi的吸收。
MmPHT1;5通过促进山荆子对Pi的吸收,在增强低Pi胁迫方面发挥了重要作用。