Department of Botany, University of Rajshahi, Rajshahi, 6205, Bangladesh.
Department of Genetics, Faculty of Agriculture, Alexandria University Alexandria, Alexandria, Egypt.
Sci Rep. 2021 Mar 10;11(1):5537. doi: 10.1038/s41598-021-85147-z.
Iron (Fe) deficiency in plants hinders growth and yield. Thus, this study aims to elucidate the responses and molecular characterization of genes in Fe-deficient sunflower. The study was conducted on 14 days-old sunflower plants cultivated in hydroponic culture under Fe-sufficient and Fe-deficient conditions. The Fe-starved sunflower showed substantial decrease in plant biomass, SPAD score, quantum yield efficiency of PSII (Fv/Fm), photosynthetic performance index (Pi_ABS). Further, Fe shortage reduced Fe and Zn concentrations in roots and shoots, accompanied by a marked decrease of HaNramp1 and HaZIP1 expression in roots, suggesting the association of Zn status contributing to photosynthetic inefficiency in sunflower. The ferric chelate reductase (FCR) activity, along with HaFRO2 and HaIRT1 transcripts, were constitutively expressed, suggesting that sunflower plants can regulate FCR activity, although the lack of bioavailable Fe in the rhizosphere strongly corresponds to the limited Fe uptake in sunflower. The substantial increase of proton extrusion in roots and the localization of Fe-related genes in the plasma membrane are also evident in sunflower as common responses to Fe-deficiency by this Strategy I plant species. Analysis showed that three motifs of Fe-related proteins were linked to the ZIP zinc transporter. The interactome map revealed the close partnership of these Fe-related genes in addition to FRU gene encoding putative transcription factor linked to Fe uptake response. The cis-regulatory analysis of promoter suggested the involvement of auxin, salicylic acid, and methyl jasmonate-responsive elements in the regulatory process in response to Fe deficiency. These findings may be beneficial to develop Fe-efficient sunflower plants through breeding or genome editing approaches.
植物缺铁会阻碍生长和产量。因此,本研究旨在阐明向日葵缺铁时的响应及其基因的分子特征。该研究在水培条件下对 14 天大的向日葵进行,在铁充足和铁缺乏条件下进行培养。缺铁的向日葵表现出植物生物量、SPAD 评分、PSII(Fv/Fm)量子产量效率、光合性能指数(Pi_ABS)显著下降。此外,铁缺乏导致根和茎中的铁和锌浓度降低,根中的 HaNramp1 和 HaZIP1 表达明显下降,表明锌的状态与向日葵光合作用效率降低有关。铁螯合还原酶(FCR)活性以及 HaFRO2 和 HaIRT1 转录物持续表达,表明向日葵植物可以调节 FCR 活性,尽管根际中生物可利用的铁缺乏强烈对应于向日葵中有限的铁吸收。质子外排在根中的大量增加以及 Fe 相关基因在质膜中的定位也是向日葵对这种策略 I 植物缺铁的共同响应。分析表明,三个 Fe 相关蛋白基序与 ZIP 锌转运体有关。互作图谱显示,这些 Fe 相关基因与 FRU 基因(编码与 Fe 吸收反应相关的假定转录因子)密切相关。启动子的顺式调控分析表明,生长素、水杨酸和茉莉酸甲酯响应元件参与了对 Fe 缺乏的响应调控过程。这些发现可能有助于通过培育或基因组编辑方法开发高效铁的向日葵植物。