华北农学报 ›› 2020, Vol. 35 ›› Issue (4): 8-14. doi: 10.7668/hbnxb.20190371

所属专题: 生物技术

• 作物遗传育种·种质资源·生物技术 • 上一篇    下一篇

拟南芥半胱氨酸蛋白酶抑制剂基因 AtCYS6克隆及功能分析

郭坤元1,2, 张欣欣3   

  1. 1. 湖北省农业科学院 中药材研究所, 国家中药材产业技术体系恩施综合试验站, 湖北 恩施 445000;
    2. 湖北省农业科技创新中心 中药材分中心, 湖北 恩施 445000;
    3. 东北林业大学 盐碱地生物资源环境研究中心, "东北盐碱植被恢复与重建"教育部重点实验室, 黑龙江 哈尔滨 150040
  • 收稿日期:2020-05-10 出版日期:2020-08-28
  • 通讯作者: 张欣欣(1979-),女,黑龙江大庆人,教授,博士,博士生导师,主要从事逆境胁迫和营养缺乏有应答的重要功能基因的分子机理研究。
  • 作者简介:郭坤元(1986-),男,湖北宣恩人,助理研究员,博士,主要从事药用植物资源开发与利用研究。
  • 基金资助:
    国家现代农业产业技术体系建设专项(CARS-21);湖北省中央引导地方科技发展专项(2018ZYYD013);湖北省技术创新专项(鄂西民族专项)(2017AKB075);恩施州科技计划研究与开发项目(D20180016)

Molecular Cloning and Functional Analysis of Cysteine Protease Inhibitor Gene AtCYS6 in Arabidopsis thaliana

GUO Kunyuan1,2, ZHANG Xinxin3   

  1. 1. Institute of Chinese Herbal Medicinal Materials, Hubei Academy of Agricultural Sciences, National Traditional Chinese Medicines Herbal Technology System Enshi Comprehensive Test Station, Enshi 445000, China;
    2. Hubei Agricultural Science and Technology Innovation Center, Chinese Medicinal Materials Sub-center, Enshi 445000, China;
    3. Research Center for Biological Resources and Environment of Saline Alkali Land, Northeast Forestry University, "Restoration and Reconstruction of Saline Alkali Vegetation in Northeast China", Key Laboratory of the Ministry of Education, Harbin 150040, China
  • Received:2020-05-10 Published:2020-08-28

摘要: 为了研究拟南芥半胱氨酸蛋白酶抑制剂AtCYS6基因在植物生长发育过程中的作用与功能,从拟南芥中克隆了半胱氨酸蛋白酶抑制剂AtCYS6基因,并对该基因进行生物信息学分析,亚细胞定位分析,蛋白质诱导、表达、纯化及功能研究。结果表明,AtCYS6蛋白等电点为5.85,化学式为C1179H1848N322O348S6,共含有3 703个原子数,为亲水性蛋白;AtCYS6与十字花科的荠菜、荠蓝的同源性较高,同源性分别为81.1%,80.3%,同水稻、玉米和大豆的同源性较低,同源性分别为55.5%,54.3%,56.6%,且在氨基酸序列中间具有高度保守的Q-V-G (Gln-Val-Gly)序列;同时进化树分析显示AtCYS6与同属于十字花科的荠菜、荠蓝的亲缘性较近,同水稻、玉米、高粱、谷子等禾本科植物的亲缘性较远;亚细胞定位结果显示其定位于细胞质,与预测结果相符合;蛋白质诱导、表达和纯化得到大小约为52 ku的融合蛋白,其中AtCYS6蛋白质的分子量约为26 ku,与预测值相符合;Western Blot分析显示,诱导表达的融合蛋白正确翻译表达,且没有出现结构上的断裂或者降解的情况;蛋白酶活性分析表明,AtCYS6对木瓜蛋白酶具有抑制作用。研究结果可以为下一步在植物体内研究该基因的相关机理作用提供基础。

关键词: 拟南芥, 半胱氨酸蛋白酶抑制剂, 亚细胞定位, 原核表达, 酶活性

Abstract: In order to study the role and function of the cysteine protease inhibitor AtCYS6 gene in plant growth and development,the AtCYS6 gene was cloned from Arabidopsis thaliana. Bioinformatics analysis,subcellular localization analysis,protein induction,expression,purification and functional were carried out to study this gene. The results showed that the isoelectric point of AtCYS6 protein was 5.85,the chemical formula was C1179H1848N322O348S6,which contained 3 703 atoms and it was a hydrophilic protein;AtCYS6 had high homology with Capsella rubella and Camelina sativa,the homology was 81.1% and 80.3% respectively,and it had low homology with Oryza sativa, Zea mays and Glycine max,the homology was 55.5%,54.3% and 56.6% respectively,among the amino acid sequences,there was a highly conserved Q-V-G (Gln-Val-Gly) sequence;evolutionary tree analysis showed that AtCYS6 was closely related to Capsella rubella and Camelina sativa,but far from Oryza sativa, Zea mays, Sorghum bicolor and Setaria italic;subcellular localization results showed that it was located in cytoplasm,which was consistent with the predicted results;the fusion protein was induced,expressed and purified to be about 52 ku in size,the molecular weight of AtCYS6 protein was about 26 ku,which accorded with the predicted value;Western Blot analysis showed that the fusion protein was correctly translated and expressed without structural breakage or degradation;enzyme activity analysis showed that AtCYS6 had inhibitory effect on papain. The results of this study provide a basis for further study of the related mechanism of AtCYS6 in plants.

Key words: Arabidopsis thaliana, Cysteine protease inhibitor, Subcellular localization, Prokaryotic expression, Enzyme activity

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引用本文

郭坤元, 张欣欣. 拟南芥半胱氨酸蛋白酶抑制剂基因 AtCYS6克隆及功能分析[J]. 华北农学报, 2020, 35(4): 8-14. doi: 10.7668/hbnxb.20190371.

GUO Kunyuan, ZHANG Xinxin. Molecular Cloning and Functional Analysis of Cysteine Protease Inhibitor Gene AtCYS6 in Arabidopsis thaliana[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2020, 35(4): 8-14. doi: 10.7668/hbnxb.20190371.

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