Im Jong Hee, Yoo Sang-Dong
Department of Life Sciences, College of Life Sciences and Biotechnology, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul, 136-701, Korea.
Methods Mol Biol. 2014;1171:3-12. doi: 10.1007/978-1-4939-0922-3_1.
Mitogen-Activated Protein Kinase (MAPK) cascade is one of the main signaling components mediating abiotic and biotic stress and hormone information in plants. Plant MAPK study has been impeded with a genetic approach using a long-term phenotypic analysis in spite of the transient nature of the protein kinase signaling. Arabidopsis leaf mesophyll protoplasts provide a versatile resource for diverse cell-based assays to acquire immediate molecular and biochemical responses with transient expression of MAPK cascade components of interests. Thus, it is an attractive tool for a high-throughput functional analysis of Arabidopsis MAPK cascade signaling. However, transient expression in Arabidopsis mesophyll protoplast (TEAMP) system requires mastered skills for protoplast preparation and handling to achieve steady and stable data. Here, we have described two analytical methods for MAPK cascade signaling using TEAMP system.
丝裂原活化蛋白激酶(MAPK)级联是介导植物非生物和生物胁迫以及激素信息的主要信号传导成分之一。尽管蛋白激酶信号传导具有瞬时性,但植物MAPK的研究一直受到长期表型分析的遗传方法的阻碍。拟南芥叶片叶肉原生质体为各种基于细胞的分析提供了一种通用资源,可通过瞬时表达感兴趣的MAPK级联成分来获得即时的分子和生化反应。因此,它是拟南芥MAPK级联信号高通量功能分析的一个有吸引力的工具。然而,拟南芥叶肉原生质体瞬时表达(TEAMP)系统需要掌握原生质体制备和处理技能,以获得稳定可靠的数据。在这里,我们描述了两种使用TEAMP系统分析MAPK级联信号的方法。