Lu Zheng , Xiangxiang Meng , Wenfeng Li , Yinglong Chen , Renfang Shen , Ping Lan
{"title":"Regulation of iron homeostasis by IMA1 and bHLH104 under phosphate starvation in Arabidopsis","authors":"Lu Zheng , Xiangxiang Meng , Wenfeng Li , Yinglong Chen , Renfang Shen , Ping Lan","doi":"10.1016/j.jplph.2025.154445","DOIUrl":null,"url":null,"abstract":"<div><div>Phosphate (Pi) starvation disrupts iron (Fe) nutrition at phenotypic, physiological, and transcriptional levels. The alteration of Fe homeostasis plays an important role in the adaptive response to Pi starvation. However, utilizing the antagonistic mechanism between P and Fe nutrition to improve adaptation to Pi deficiency in plants still needs to be explored. Here, we constructed inducible and constitutive expression of Fe regulators <em>IMA1</em> and <em>bHLH104</em>, driven by the <em>CaMV 35S</em> promoter and the promoters of Pi-starvation responsive genes (<em>proIPS1</em> and <em>proPHT1;4</em>), respectively. The Fe regulators <em>bHLH104</em> and <em>IMA1</em> were successfully upregulated in a constitutive and inducible manner under Pi deficiency in these transgenic plants. Regardless of Pi condition, upregulation of <em>bHLH104</em> and <em>IMA1</em> had no significant influence on primary root length or root Fe distribution. Nevertheless, the upregulation of <em>bHLH104</em> and <em>IMA1</em> induced Fe accumulation in the shoots of transgenic plants, particularly under Pi deficiency. Correspondingly, shoot chlorophyll content increased under Fe deficiency in the transgenic plants. In addition, <em>in situ</em> Fe<sup>III</sup> distribution revealed that <em>bHLH104</em> and <em>IMA1</em> likely interfere with Fe distribution through different pathways. The inducible upregulation of <em>IMA1</em> significantly led to shoot zinc (Zn) accumulation under Pi deficiency, while the inducible upregulation of <em>bHLH104</em> resulted in a decrease in shoot Zn and manganese (Mn) contents. The enhancement of Fe and Zn accumulation under the inducible expression of <em>IMA1</em> under Pi deficiency was attributed to the induction of high expression of key Fe-uptake genes <em>FRO2</em> and <em>IRT1</em>. The expression of the Zn and Mn uptake genes was also affected in these transgenic plants, which correlated with the changes in Zn and Mn contents. Overall, <em>IMA1</em> is an excellent candidate for enhancing plant Fe and Zn accumulation and can be specifically induced under conditions of Pi deficiency.</div></div>","PeriodicalId":16808,"journal":{"name":"Journal of plant physiology","volume":"306 ","pages":"Article 154445"},"PeriodicalIF":4.0000,"publicationDate":"2025-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of plant physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0176161725000276","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Phosphate (Pi) starvation disrupts iron (Fe) nutrition at phenotypic, physiological, and transcriptional levels. The alteration of Fe homeostasis plays an important role in the adaptive response to Pi starvation. However, utilizing the antagonistic mechanism between P and Fe nutrition to improve adaptation to Pi deficiency in plants still needs to be explored. Here, we constructed inducible and constitutive expression of Fe regulators IMA1 and bHLH104, driven by the CaMV 35S promoter and the promoters of Pi-starvation responsive genes (proIPS1 and proPHT1;4), respectively. The Fe regulators bHLH104 and IMA1 were successfully upregulated in a constitutive and inducible manner under Pi deficiency in these transgenic plants. Regardless of Pi condition, upregulation of bHLH104 and IMA1 had no significant influence on primary root length or root Fe distribution. Nevertheless, the upregulation of bHLH104 and IMA1 induced Fe accumulation in the shoots of transgenic plants, particularly under Pi deficiency. Correspondingly, shoot chlorophyll content increased under Fe deficiency in the transgenic plants. In addition, in situ FeIII distribution revealed that bHLH104 and IMA1 likely interfere with Fe distribution through different pathways. The inducible upregulation of IMA1 significantly led to shoot zinc (Zn) accumulation under Pi deficiency, while the inducible upregulation of bHLH104 resulted in a decrease in shoot Zn and manganese (Mn) contents. The enhancement of Fe and Zn accumulation under the inducible expression of IMA1 under Pi deficiency was attributed to the induction of high expression of key Fe-uptake genes FRO2 and IRT1. The expression of the Zn and Mn uptake genes was also affected in these transgenic plants, which correlated with the changes in Zn and Mn contents. Overall, IMA1 is an excellent candidate for enhancing plant Fe and Zn accumulation and can be specifically induced under conditions of Pi deficiency.
期刊介绍:
The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication.
The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.