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拟南芥AtHHR2与DREB2C的相互作用研究
引用本文:蔡潇潇,刘志斌,王健美,李旭锋. 拟南芥AtHHR2与DREB2C的相互作用研究[J]. 四川大学学报(自然科学版), 2018, 55(4): 860-864
作者姓名:蔡潇潇  刘志斌  王健美  李旭锋
作者单位: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
基金项目:国家转基因专项(2016ZX08009003-002-001); 国家自然科学基金(31671455)
摘    要:已有研究表明拟南芥Highly Homologous RING domain 2(At5g43200,命名为AtHHR2)基因在盐胁迫中起正调控作用,并且其同源基因AtHHR3基因在酵母双杂交实验筛选中与DREB2C基因有相互作用.本研究利用体外、体内蛋白质相互作用实验以及生物化学方法进一步探究了AtHHR2的功能性.体外Pull-down实验证实了AtHHR2与DREB2C有体外的相互作用.体外泛素化实验进一步验证了它们之间的相互作用,且AtHHR2起到E3连接酶的作用.为了进一步确定它们的关系,我们用双分子荧光互补实验,在体内分别验证了AtHHR2与DREB2C之间确实有相互作用.综上所述在拟南芥中AtHHR2与DREB2C有相互作用关系,且AtHHR2起到E3连接酶的作用.

关 键 词:AtHHR2;RING finger E3连接酶;拟南芥;DREB2C
收稿时间:2017-03-20
修稿时间:2017-05-20

Analysis of the interaction between AtHHR2 and DREB2C in Arabidopsis thaliana
CAI Xiao-Xiao,LIU Zhi-Bin,WANG Jian-Mei and LI Xu-Feng. Analysis of the interaction between AtHHR2 and DREB2C in Arabidopsis thaliana[J]. Journal of Sichuan University (Natural Science Edition), 2018, 55(4): 860-864
Authors:CAI Xiao-Xiao  LIU Zhi-Bin  WANG Jian-Mei  LI Xu-Feng
Affiliation:Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University,Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University,Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University,Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University
Abstract:A previous report has revealed that AtHHR2 (At5g43200) played a positive regulatory role in Arabidopsis thaliana in salt stress, and its homologous gene AtHHR3 has interaction with DREB2C gene in yeast twohybrid test. In this study, in vitro and in vivo protein interaction assays and biochemical methods were used to further explore the functionality of AtHHR2. And Pulldown result validated the interaction between AtHHR2 and DREB2C in vitro. And the ubiquitination analysis demonstrated that AtHHR2 acted as an E3 ligase of DREB2C, further confirming the interaction between AtHHR2 and DREB2C. Furthermore, bimolecular fluorescence complementation assay results showed that AtHHR2 did have interaction with DREB2C in vivo. In summary, the AtHHR2 interacts with DREB2C and acts as an E3 ligase.
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