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锰毒性对番茄(Solanum lycopersicum)根系蛋白质图谱的影响,采用两种互补的蛋白质组学方法(二维电泳和鸟枪法分析)揭示。

Effects of manganese toxicity on the protein profile of tomato (Solanum lycopersicum) roots as revealed by two complementary proteomic approaches, two-dimensional electrophoresis and shotgun analysis.

机构信息

Plant Stress Physiology Group, Plant Nutrition Department, Aula Dei Experimental Station, CSIC, P.O. Box 13034, 50080 Zaragoza, Spain.

United Graduate School of Agricultural Sciences, Iwate University, Morioka 020-8550, Japan; Cryobiofrontier Research Center, Faculty of Agriculture, Iwate University, Morioka 020-8550, Japan.

出版信息

J Proteomics. 2018 Aug 15;185:51-63. doi: 10.1016/j.jprot.2018.06.016. Epub 2018 Jun 25.

Abstract

The aim of this work was to assess the effects of manganese (Mn) toxicity on the proteome of tomato roots using two proteomic approaches, shotgun and two-dimensional electrophoresis. The shotgun approach yielded 367 reliable proteins, whereas the 2-DE approach detected 340 consistent spots. The 2-DE method found 54 proteins changing in relative abundance in the excess Mn treatment, whereas the shotgun detected changes in 118 proteins. Only 7% of the differential proteins were found by both methods, illustrating their complementary nature. Metabolic pathways most affected were protein metabolism, oxido-reductases and signaling. Results support that Mn toxicity alters the protein turnover and impairs energy production in roots, leading to changes in glycolysis, pyruvate metabolism, TCA and oxidative phosphorylation. Excess Mn also induced changes in peroxidases and hydrolases participating in cell wall lignification and suberization and activated plant defense mechanisms, with changes occurring via pathogenesis-related proteins as well as peroxidases. Finally, Mn toxicity elicited regulatory mechanisms and affected the abundance of root nutrient reservoir proteins. The overall analysis of the differential root proteome upon Mn toxicity suggests a general slowdown of metabolic activities, especially energy production, cell wall integrity and protein turnover, which occurs in parallel with increases in stress related proteins.

摘要

本工作旨在使用两种蛋白质组学方法——shotgun 和二维电泳——来评估锰(Mn)毒性对番茄根系蛋白质组的影响。shotgun 方法产生了 367 个可靠的蛋白质,而 2-DE 方法检测到 340 个一致的斑点。2-DE 方法发现过量 Mn 处理下有 54 种蛋白质的相对丰度发生变化,而 shotgun 则检测到 118 种蛋白质的变化。两种方法都发现了 7%的差异蛋白,这说明了它们的互补性。受影响最大的代谢途径是蛋白质代谢、氧化还原酶和信号转导。结果表明,Mn 毒性改变了蛋白质周转,损害了根系的能量产生,导致糖酵解、丙酮酸代谢、三羧酸循环和氧化磷酸化发生变化。过量 Mn 还诱导了参与细胞壁木质化和栓质化的过氧化物酶和水解酶的变化,并激活了植物防御机制,通过与发病相关的蛋白质以及过氧化物酶发生变化。最后,Mn 毒性引发了调节机制,并影响了根养分库蛋白的丰度。Mn 毒性对根系蛋白质组的整体分析表明,代谢活性特别是能量产生、细胞壁完整性和蛋白质周转普遍减慢,同时与应激相关的蛋白质增加。

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