紫苏叶片响应镉胁迫的蛋白质差异表达分析

Analysis of differentially expressed proteins in Perilla frutescens (L.) Britt. leaves under cadmium stress

  • 摘要: 为阐明紫苏Perilla frutescens (L.) Britt.响应镉胁迫的分子机制, 应用营养液加镉法, 采用蛋白质组学技术分析了紫苏叶片响应镉胁迫3周的蛋白质表达差异。结果表明, 镉胁迫下紫苏叶片有25个蛋白发生差异表达, 其中20个蛋白质得到LC-MS/MS鉴定: 光合作用相关蛋白3个, 能量代谢相关蛋白11个, 胁迫相关蛋白1个, 蛋白质代谢相关蛋白2个, 基因表达相关蛋白1个, 结构蛋白1个, 生物合成与解毒相关蛋白1个。在浓度为2.0 mg·kg-1、5.0 mg·kg-1、10.0 mg·kg-1镉胁迫下, 紫苏叶片中ATP合成酶、丝氨酸羧肽酶、植物细胞色素P450均上调表达, Rubisco大亚基、核糖体蛋白S3和肌动蛋白表达均下调。光合系统Ⅱ稳定/装配因子HCF136及胁迫反应蛋白乙酰辅酶A硫酯酶在低浓度镉(2 mg·kg-1)处理下表达上调, 在高浓度镉(5 mg·kg-1, 10 mg·kg-1)处理下表达下调; 磷酸核酮糖激酶/尿苷激酶家族蛋白在2 mg·kg-1和5 mg·kg-1镉处理时表达上调, 10 mg·kg-1镉处理时不变; 逆转录转座子蛋白在10 mg·kg-1镉处理时表达下调。可见, 紫苏叶片通过增强能量代谢、降低光合作用、改变蛋白代谢与基因表达和提高解毒能力, 增强了镉耐性。

     

    Abstract: To elucidate the mechanism of tolerant of exposed Perilla frutescens (L.) Britt. to cadmium stress, a set of hydroponic culture experiments were set up to analyze the differential expressions of proteins in P. frutescens leaves after 3 weeks of exposure. The study used two-dimensional electrophoresis technique and added Cd2+ to hydroponic solutions of the hydroponic culture experiments. Based on the results, 25 proteins changed in P. frutescens leaves and 20 of them were identified by LC-MS/MS analysis. The identified proteins included 3 proteins related to photosynthesis, 11 proteins related to energy metabolism, 1 protein related to stress, 2 proteins related to protein metabolism, 1 protein related to gene expression, 1 structural protein, and 1 protein related to biosynthesis and detoxication. Under Cd2+ concentrations of 2.0 mg·kg-1, 5.0 mg·kg-1 and 10.0 mg·kg-1, ATP synthase, serine carboxypeptidases and plant cytochrome P450 up-regulated in P. frutescens leaves, but oxygenase large subunit, ribosomal protein S3 and actin down-regulated in P. frutescens leaves. Furthermore, photosystem Ⅱ stability/assembly factor HCF136 and acyl-CoA thioesterase up-regulated in low Cd2+ concentration of 2 mg·kg-1, but down-regulated in higher Cd2+ concentrations of 5 mg·kg-1 and 10 mg·kg-1. Phosphoribulokinase/uridine kinase family protein up-regulated under 2 mg·kg-1 and 5 mg·kg-1 Cd2+ concentrations, but no difference was detected under 10 mg·kg-1 Cd2+ concentration. Additionally, retrotransposon protein involved in gene expression down-regulated under 10 mg·kg-1 Cd2+ concentration. The results indicated that P. frutescens strengthened energy metabolism, reduced photosynthesis, altered protein metabolism and gene expression, and improved detoxification under Cd2+ stress, and thereby enhanced P. frutescens cadmium tolerance.

     

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