蛋白质组学分析揭示水稻地上部对缺铁和高铁胁迫的响应
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中图分类号:

Q946.1

基金项目:

国家自然科学基金面上项目(32070279)和江苏省自然科学基金面上项目(BK20221560)资助


Proteomic Dissection of the Rice Shoots in Response to Iron Deficiency and Excess
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Supported by the National Natural Science Foundation of China (No. 32070279) and the Natural Science Foundation of Jiangsu Province, China (No. BK20221560)

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    摘要:

    铁在矿质土壤中含量丰富,但在中性和碱性土壤中大多以不易被植物吸收利用的氧化物或氢氧化物形式存在;稻田土壤在淹水条件时氧化还原电位较低,大量铁以易被植物吸收利用的亚铁形式存在。土壤中铁的生物有效性过低或过高均会导致植物的生长发育受阻。本研究对缺铁(0 μmol·L-1)、铁充足(40 μmol·L-1)和高铁(350和500 μmol·L-1)条件生长的水稻地上部进行了非标记蛋白质组学分析。结果显示,与铁充足条件相比,缺铁和两种浓度的高铁胁迫水稻中分别有130、157和118个蛋白质的丰度发生显著变化。基因本体富集分析显示,缺铁和高铁胁迫下的差异蛋白在初级代谢过程、有机氮化合物代谢过程、蛋白质代谢过程和细胞成分组织或生物发生等生物学过程均显著富集;差异蛋白还参与核糖体、光合作用和氧化磷酸化等代谢途径。缺铁胁迫显著影响参与苯丙烷类物质和辅助因子生物合成的蛋白质丰度,而高铁胁迫则引起氨基酸生物合成过程的蛋白质丰度发生显著变化。本研究发掘到一系列可用于水稻铁高效育种工作的候选蛋白,还发现了一些功能未知的差异蛋白可作为后续水稻铁胁迫响应的研究目标,同时为理解植物应对铁胁迫的完整响应网络提供了补充信息。

    Abstract:

    【Objective】In calcareous soils, iron (Fe) generally exists in the form of oxides or hydroxides, which is not conducive to plant absorption and utilization, thus frequently causing Fe deficiency in plants. In flooded acidic soils, such as paddy soil, due to conditions of irrigation and drainage and alternate cultivation of water and drought, the redox potential of the soil is low and ferric Fe is reduced to be ferrous. The ferrous Fe is readily absorbed and utilized, resulting in excessive Fe absorption by plants. Fe deficiency and excess are limiting factors affecting rice yield and quality. Fe deficiency leads to chlorosis and reduces plant growth while Fe overload is toxic for plants, with a typical symptom of leaf bronzing. Several transcriptome analyses have been performed to investigate the responses under Fe stress. However, a comprehensive dissection of the entire Fe-responsive profile at the protein level is still lacking. It is necessary to analyze the rice responses under Fe deficiency and Fe excess using proteomic analysis. 【Method】 In this study, a label-free proteomic analysis was performed on rice shoots grown in Fe-deficient (0 μmol·L-1), Fe-sufficient (40 μmol·L-1), and Fe-excess (350 and 500 μmol·L-1) conditions. 【Result】Results showed that 130, 157 and 118 differentially accumulated proteins (DAPs) were identified under Fe deficiency and two concentrations of Fe excess stresses, respectively, compared with Fe sufficient conditions. Gene ontology enrichment analysis of the DAPs revealed that primary metabolic process, organonitrogen compound metabolic process, response to stimulus, and oxidative stress responses were significantly enriched under both Fe deficiency and excess stresses. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that DAPs under Fe deficiency and Fe excess were commonly enriched in metabolic processes like the ribosome, photosynthesis, and oxidative phosphorylation. Notably, the abundance of proteins involved in phenylpropanoid biosynthesis and biosynthesis of cofactors was mainly affected by Fe deficiency, while the abundance of proteins involved in the biosynthesis of amino acids was mainly influenced by Fe excess. Under Fe excess stress, the abundance of enzymes involved in amino acid metabolism was decreased, indicating a reduction in the content of plant-synthesized amino acids. However, the increased abundance of transketolase involved in photosynthesis and secondary metabolism probably reduced the inhibitory effect induced by Fe stress. Ribosomal proteins S16, Os03g0798600 and RPL17 may play important roles in response to Fe deficiency and Fe excess stresses, but the exact functions of these proteins under Fe stress are still unknown. Several novel proteins which may play potential roles in rice Fe homeostasis were also predicted in this study. 【Conclusion】Overall, our results indicate both Fe deficiency and Fe excess stresses affected photosynthesis and ribosomal metabolism. The synthesis of phenylpropane was mainly affected by Fe deficiency, while amino acid metabolism was mainly affected by Fe excess in the shoots of rice. The findings will provide some information for the exploration of key factors for the efficient absorption and utilization of Fe.

    参考文献
    [1] Li W F,Zhu H Y,Lan P. Research progress of iron homeostasis regulation in strategy Ⅰ plants[J]. Soils,2021,53(6):1101-1106. [李文凤,朱海焰,兰平. 策略Ⅰ植物铁吸收稳态调控研究进展[J]. 土壤,2021,53(6):1101-1106.]
    [2] Wang Y Q,Li Y H,Zhu Z K,et al. The Effect of iron oxides on mineralization,transformation and priming effect of acetate in anoxic paddy soils[J]. Acta Pedologica Sinica,2022,DOI:10.11766/trxb202105270277. [王云秋,李宇虹,祝贞科,等. 铁氧化物对厌氧水稻土中乙酸矿化、转化及其激发效应的影响[J]. 土壤学报,2022,DOI:10.11766/trxb202105270277.]
    [3] Zhang X,Zhang D,Sun W,et al. The adaptive mechanism of plants to iron deficiency via iron uptake,transport,and homeostasis[J]. International Journal of Molecular Sciences,2019,20(10):2424.
    [4] Suh H J,Kim C S,Lee J Y,et al. Photodynamic effect of iron excess on photosystem II function in pea plants[J]. Photochemistry and Photobiology,2002,75(5):513-518.
    [5] Zhang N N,Shangguan Z P,Chen J. Molecular physiological mechanism and regulation of plant responses to iron deficiency stress[J]. Journal of Plant Nutrition and Fertilizers,2018,24(5):1365-1377. [张妮娜,上官周平,陈娟. 植物应答缺铁胁迫的分子生理机制及其调控[J]. 植物营养与肥料学报,2018,24(5):1365-1377.]
    [6] Ishimaru Y,Suzuki M,Tsukamoto T,et al. Rice plants take up iron as an Fe3+-phytosiderophore and as Fe2+[J]. The Plant Journal,2006,45(3):335-346.
    [7] Inoue H,Kobayashi T,Nozoye T,et al. Rice OsYSL15 is an iron-regulated iron(III)-deoxymugineic acid transporter expressed in the roots and is essential for iron uptake in early growth of the seedlings[J]. Journal of Biological Chemistry,2009,284(6):3470-3479.
    [8] Kabir A H,Paltridge N G,Able A J,et al. Natural variation for Fe-efficiency is associated with upregulation of strategy I mechanisms and enhanced citrate and ethylene synthesis in Pisum sativum L[J]. Planta,2012,235(6):1409-1419.
    [9] Jin C W,He Y F,Tang C X,et al. Mechanisms of microbially enhanced Fe acquisition in red clover(Trifolium pratense L.)[J]. Plant,Cell and Environment,2006,29(5):888-897.
    [10] Becker M,Asch F. Iron toxicity in rice-conditions and management concepts[J]. Journal of Plant Nutrition and Soil Science,2005,168(4):558-573.
    [11] Briat J F,Duc C,Ravet K,et al. Ferritins and iron storage in plants[J]. Biochimica et Biophysica Acta,2010,1800(8):806-814.
    [12] Aung M S,Masuda H,Kobayashi T,et al. Physiological and transcriptomic analysis of responses to different levels of iron excess stress in various rice tissues[J]. Soil Science and Plant Nutrition,2018,64(3):370-385.
    [13] Huang H L,Ullah F,Zhou D X,et al. Mechanisms of ROS regulation of plant development and stress responses[J]. Frontiers in Plant Science,2019,10:800.
    [14] Bashir K,Hanada K,Shimizu M,et al. Transcriptomic analysis of rice in response to iron deficiency and excess[J]. Rice,2014,7(1):18.
    [15] Chen L,Ding C Q,Zhao X F,et al. Differential regulation of proteins in rice(Oryza sativa L.)under iron deficiency[J]. Plant Cell Reports,2015,34(1):83-96.
    [16] Kar S,Mai H J,Khalouf H,et al. Comparative transcriptomics of lowland rice varieties uncovers novel candidate genes for adaptive iron excess tolerance[J]. Plant & Cell Physiology,2021,62(4):624-640.
    [17] Chaiwong N,Bouain N,Prom-U-Thai C,et al. Interplay between silicon and iron signaling pathways to regulate silicon transporter Lsi1 expression in rice[J]. Frontiers in Plant Science,2020,11:1065.
    [18] Lan P,Li W,Schmidt W. Complementary proteome and transcriptome profiling in phosphate-deficient arabidopsis roots reveals multiple levels of gene regulation[J]. Molecular & Cellular Proteomics,2012,11(11):1156-1166.
    [19] Wiśniewski J R,Zougman A,Nagaraj N,et al. Universal sample preparation method for proteome analysis[J]. Nature Methods,2009,6(5):359-362.
    [20] Reimand J,Isserlin R,Voisin V,et al. Pathway enrichment analysis and visualization of omics data using g:Profiler,GSEA,Cytoscape and EnrichmentMap[J]. Nature Protocols,2019,14(2):482-517.
    [21] Wu T Z,Hu E Q,Xu S B,et al. ClusterProfiler 4.0:A universal enrichment tool for interpreting omics data[J]. The Innovation,2021,2(3):100141.
    [22] Rogalski M,Ruf S,Bock R. Tobacco plastid ribosomal protein S18 is essential for cell survival[J]. Nucleic Acids Research,2006,34(16):4537-4545.
    [23] Ehrnthaler M,Scharff L B,Fleischmann T T,et al. Synthetic lethality in the tobacco plastid ribosome and its rescue at elevated growth temperatures[J]. The Plant Cell,2014,26(2):765-776.
    [24] Schultes N P,Sawers R J H,Brutnell T P,et al. Maize high chlorophyll fluorescent 60 mutation is caused by an ac disruption of the gene encoding the chloroplast ribosomal small subunit protein 17[J]. The Plant Journal,2000,21(4):317-327.
    [25] Wang W J,Zheng K L,Gong X D,et al. The rice tcd11 encoding plastid ribosomal protein S6 is essential for chloroplast development at low temperature[J]. Plant Science,2017,259:1-11.
    [26] Mallikarjuna M G,Thirunavukkarasu N,Sharma R,et al. Comparative transcriptome analysis of iron and zinc deficiency in maize(Zea mays L.)[J]. Plants,2020,9(12):1812.
    [27] Khozaei M,Fisk S,Lawson T,et al. Overexpression of plastid transketolase in tobacco results in a thiamine auxotrophic phenotype[J]. The Plant Cell,2015,27(2):432-447.
    [28] Yin Z K,Stead D,Walker J,et al. A proteomic analysis of the salt,cadmium and peroxide stress responses in Candida albicans and the role of the Hog1 stress-activated MAPK in regulating the stress-induced proteome[J]. Proteomics,2009,9(20):4686-4703.
    [29] Lee D G,Ahsan N,Lee S H,et al. A proteomic approach in analyzing heat-responsive proteins in rice leaves[J]. Proteomics,2007,7(18):3369-3383.
    [30] Galili G. New insights into the regulation and functional significance of lysine metabolism in plants[J]. Annual Review of Plant Biology,2002,53:27-43.
    [31] Caldwell R W,Rodriguez P C,Toque H A,et al. Arginase:A multifaceted enzyme important in health and disease[J]. Physiological Reviews,2018,98(2):641-665.
    [32] Winter G,Todd C D,Trovato M,et al. Physiological implications of arginine metabolism in plants[J]. Frontiers in Plant Science,2015,6:534.
    [33] Sun H W,Feng F,Liu J,et al. The interaction between auxin and nitric oxide regulates root growth in response to iron deficiency in rice[J]. Frontiers in Plant Science,2017,8:2169.
    [34] Sharma A,Badola P K,Bhatia C,et al. Primary transcript of miR858 encodes regulatory peptide and controls flavonoid biosynthesis and development in Arabidopsis[J]. Nature Plants,2020,6(10):1262-1274.
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张欣,王若男,沈仁芳,兰平.蛋白质组学分析揭示水稻地上部对缺铁和高铁胁迫的响应[J].土壤学报,2024,61(1):118-128. DOI:10.11766/trxb202203150109 ZHANG Xin, WANG Ruonan, SHEN Renfang, LAN Ping. Proteomic Dissection of the Rice Shoots in Response to Iron Deficiency and Excess[J]. Acta Pedologica Sinica,2024,61(1):118-128.

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  • 收稿日期:2022-03-15
  • 最后修改日期:2022-06-21
  • 录用日期:2022-08-11
  • 在线发布日期: 2022-08-15
  • 出版日期: 2024-01-15
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