期刊导航

论文摘要

拟南芥AtTR1对AtCPK28和AtCPK32的体外泛素化修饰研究

Investigation on ubiquitination of AtCPK28 and AtCPK32 by AtTR1 in vitro

作者:樊莉娟(四川大学生命科学学院生物资源与生态环境教育部重点实验室);陈彩丽(四川大学生命科学学院生物资源与生态环境教育部重点实验室);朱旭辉(四川大学生命科学学院生物资源与生态环境教育部重点实验室);黄奎(四川大学生命科学学院生物资源与生态环境教育部重点实验室);姚润东(四川大学生命科学学院生物资源与生态环境教育部重点实验室);王健美(四川大学生命科学学院生物资源与生态环境教育部重点实验室)

Author:FAN Li-Juan(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University);CHEN Cai-Li(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University);ZHU Xu-Hui(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University);HUANG Kui(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University);YAO Run-Dong(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University);WANG Jian-Mei(Key Laboratory of Bio-resources and Eco-environment of Ministry of Education, College of Life Sciences, Sichuan University)

收稿日期:2016-01-21          年卷(期)页码:2017,54(3):617-622

期刊名称:四川大学学报: 自然科学版

Journal Name:Journal of Sichuan University (Natural Science Edition)

关键字:拟南芥 AtTR1 AtCPK28 AtCPK32 泛素化

Key words:Arabidopsis AtTR1 AtCPK28 AtCPK32 Ubiquitination

基金项目:国家自然科学基金

中文摘要

AtTR1、AtCPK28、AtCPK32是参与非生物胁迫应答的相关蛋白,并且与Ca2+信号通路密切关联。为了分析AtTR1和AtCPK28、AtCPK32之间关系,在大肠杆菌中表达了AtTR1、AtCPK28和AtCPK32基因,纯化了表达蛋白,并在体外研究了AtTR1对AtCPK28和AtCPK32泛素化作用,结果发现AtTR1在体外能够对AtCPK28和AtCPK32进行多泛素化修饰。该结果表明AtCPK28和AtCPK32可能是AtTR1调控植物抗逆信号中的下游靶蛋白。该研究结果不仅为进一步研究AtTR1与AtCPK28和AtCPK32之间的相互作用提供了实验证据,而且为研究三者在植物非生物胁迫中的分子机制奠定了基础。

英文摘要

AtTR1, AtCPK28, and AtCPK32 are functioning in the abiotic stress response in Arabidopsis thialiana, and closely associated with the calcium signaling pathway. In order to analyze relationships between AtTR1, AtCPK28 and AtCPK32, we expressed AtTR1, AtCPK28, and AtCPK32 in Escherichia coli, purified expression proteins, and studied the ubiquitination of AtCPK28 and AtCPK32 by AtTR1 in vitro. The results showed that the AtCPK28 and AtCPK32 were multi-ubiquitylated by AtTR1 in vitro. It indicated that the AtCPK28 and AtCPK32 are potential downstream targets of AtTR1 in the regulation of stress resistance signaling pathways. These findings provided experimental evidence to further study the interactions between AtTR1, AtCPK28, and AtCPK32, and also provided some insights of their molecular mechanisms in the plant under abiotic stresses.

关闭

Copyright © 2020四川大学期刊社 版权所有.

地址:成都市一环路南一段24号

邮编:610065