H+-焦磷酸酶VP1通过与生长素内流载体AUX1相互作用增强小麦低磷耐受性。

IF 6.9 1区 生物学 Q1 PLANT SCIENCES Plant, Cell & Environment Pub Date : 2026-10-18 DOI:10.1111/pce.70970
Chengjie Xu, Huijuan Zhang, Jia Guo, Chunxiao Wang, Wanggao Ma, Yuqi Niu, Yongbin Zhou, Jun Chen, Zhaoshi Xu, Youzhi Ma, Yongkang Ren, Daizhen Sun, Ming Chen, Zhaohui Tang
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引用次数: 0

摘要

磷(P)是作物生长必需的大量营养元素,其缺乏严重限制了小麦的产量,因此强调了提高磷利用效率(PUE)对全球粮食安全的重要性。尽管质子焦磷酸酶(I型H+-焦磷酸酶,VP1, H+-PPases)在植物对非生物胁迫的响应中起着关键作用,但其在低磷(LP)胁迫下在小麦(Triticum aestivum L.)中发挥作用的分子机制仍未得到充分研究。羊草(Elymus dahuricus)是一种野生牧草,对多种环境胁迫表现出显著的抗性。本研究将一种来自羊草的vp1样基因(EdVP1)导入野生型小麦品种世麦366 (SHI366)。在低LP条件下进行的为期两年的田间试验表明,过表达EdVP1显著提高了每米穗数、籽粒产量、磷收获指数(PHI)和磷利用效率(PUE)。其中,转基因品系OE13和OE28在灌浆期的光合速率和叶绿素含量均显著提高,连续2年的平均产量较WT植株分别提高了14.25%和15.65%。此外,与SHI366相比,转基因品系根系中的磷含量显著升高。随后在缺磷条件下进行的试验证实,转基因植株的生物量积累和根系结构(RSA)均有显著改善。生理分析进一步表明,这些品系的活性氧(ROS)积累减少,抗氧化酶活性增强。综上所述,这些结果表明,来自羊草的VP1基因显著增强了小麦对缺磷的耐受性。为了阐明vp1样基因在小麦中的作用机制,我们鉴定了与EdVP1进化关系最密切、序列同源性最高的内源质膜(PM) H+-PPases基因TaVP1 (TraesCS7D02G507600),发现其在转EdVP1的小麦中表达上调。TaVP1的表达主要集中在根中,并受到缺磷和生长素(IAA)处理的强烈诱导。值得注意的是,转基因植株根部的生长素水平显著升高,同时生长素内流载体基因TaAUX1 (TraesCS3B02G401000)表达上调。体内和体外实验均证实了TaVP1和TaAUX1在质膜上的直接相互作用。此外,与下游生长素运输和应答相关的因子,以及关键的磷酸盐饥饿转录因子tapfr1,在转基因品系中表现出上调的表达模式。综上所述,这些结果揭示了一个新的机制,即H+-PPase通过与生长素信号通路的串扰增强小麦对缺磷的耐受性。
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H+-Pyrophosphatase VP1 Enhances Low Phosphorus Tolerance by Interacting With the Auxin Influx Carrier AUX1 in Wheat.

Phosphorus (P) is an essential macronutrient for crop growth, and its deficiency significantly limits wheat productivity, thereby underscoring the importance of improving phosphorus use efficiency (PUE) for global food security. Although proton-pyrophosphatase (Type I H+-pyrophosphatase, VP1, H+-PPases) plays critical roles in plant responses to abiotic stresses, the molecular mechanisms underlying its function in wheat (Triticum aestivum L.) under low-phosphorus (LP) stress remain largely unexplored. Elymus dahuricus, a wild forage grass species, exhibits notable resistance to diverse environmental stresses. In the present study, a VP1-like gene from Elymus dahuricus (EdVP1) was introduced into wild-type (WT) wheat cultivar Shimai366 (SHI366). Two-year field trials conducted under LP conditions demonstrated that overexpression of EdVP1 significantly increased spike number per meter, grain yield, phosphorus harvest index (PHI), and phosphorus use efficiency (PUE). Specifically, transgenic lines OE13 and OE28 exhibited average yield increases of 14.25% and 15.65%, respectively, relative to WT plants over two consecutive years, accompanied by improved photosynthetic rates and chlorophyll content during the grain-filling stage. Additionally, P concentrations in the roots of transgenic lines were significantly elevated compared to SHI366. Subsequent assays under phosphorus-deficient conditions confirmed substantial improvements in both biomass accumulation and root system architecture (RSA) in the transgenic lines. Physiological analyses further demonstrated reduced accumulation of reactive oxygen species (ROS) and enhanced activities of antioxidant enzymes in these lines. Collectively, these findings indicate that the VP1 gene from Elymus dahuricus markedly enhances wheat tolerance to P deficiency. To elucidate the underlying mechanisms of VP1-like genes in wheat, the endogenous plasma membrane (PM) H+-PPases gene TaVP1 (TraesCS7D02G507600), which exhibits the closest evolutionary relationship and highest sequence homology with EdVP1 among grass species, was identified and found to be upregulated in EdVP1 transgenic wheat. TaVP1 expression was predominantly localized in roots and was strongly induced by P-deficient and auxin (IAA) treatment. Notably, auxin levels were significantly increased in the roots of transgenic lines, concomitant with upregulated expression of the auxin influx carrier gene TaAUX1 (TraesCS3B02G401000). Both in vivo and in vitro assays demonstrated a direct interaction between TaVP1 and TaAUX1 at the plasma membrane. Furthermore, factors associated with downstream auxin transport and response, along with the key phosphate starvation transcription factor TaPHR1, exhibit an upregulated expression pattern in the transgenic lines. Taken together, these results reveal a novel mechanism by which H+-PPase enhances tolerance to phosphorus deficiency in wheat through crosstalk with auxin signaling pathways.

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来源期刊
Plant, Cell & Environment
Plant, Cell & Environment 生物-植物科学
CiteScore
13.30
自引率
4.10%
发文量
253
审稿时长
1.8 months
期刊介绍: Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.
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