The National Key Facility for Crop Gene Resources and Genetic Improvement/Key Laboratory of Biology and Genetic Improvement of Triticeae Crops of Agricultural Ministry, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Biotechnology Institute, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
New Phytol. 2012 Dec;196(4):1155-1170. doi: 10.1111/j.1469-8137.2012.04353.x. Epub 2012 Oct 9.
In this study, we report new insights into the function of a wheat (Triticum aestivum) MYB gene TaPIMP1 through overexpression and underexpression, and its underlying mechanism in wheat. Electrophoretic mobility shift and yeast-one-hybrid assays indicated that TaPIMP1 can bind to five MYB-binding sites including ACI, and activate the expression of the genes with the cis-element, confirming that TaPIMP1 is an MYB transcription activator. TaPIMP1-overexpressing transgenic wheat exhibited significantly enhanced resistance to the fungal pathogen Bipolaris sorokiniana and drought stresses, whereas TaPIMP1-underexpressing transgenic wheat showed more susceptibility to the stresses compared with untransformed wheat, revealing that TaPIMP1 positively modulates host-defense responses to B. sorokiniana and drought stresses. Microarray analysis showed that a subset of defense- and stress-related genes were up-regulated by TaPIMP1. These genes, including TaPIMP1, RD22, TLP4 and PR1a, were regulated by ABA and salicylic acid (SA). TaPIMP1-underexpressing transgenic wheat showed compromised induction of these stress-responsive genes following ABA and SA treatments. In summary, TaPIMP1, as a positive molecular linker, mediates resistance to B. sorokiniana and drought stresses by regulation of stress-related genes in ABA- and SA-signaling pathways in wheat. Furthermore, TaPIMP1 may provide a transgenic tool for engineering multiple-resistance wheat in breeding programs.
在这项研究中,我们通过过表达和低表达小麦(Triticum aestivum)MYB 基因 TaPIMP1,报告了其在小麦中功能的新见解及其潜在机制。电泳迁移率变动分析和酵母单杂交试验表明,TaPIMP1 可以结合包括 ACI 在内的五个 MYB 结合位点,并激活具有顺式元件的基因的表达,这证实了 TaPIMP1 是一种 MYB 转录激活因子。过表达 TaPIMP1 的转基因小麦对真菌病原体禾旋孢腔菌和干旱胁迫表现出明显增强的抗性,而 TaPIMP1 低表达的转基因小麦对胁迫的敏感性比未转化的小麦更高,这表明 TaPIMP1 正向调节宿主对禾旋孢腔菌和干旱胁迫的防御反应。微阵列分析显示,一组防御和应激相关基因被 TaPIMP1 上调。这些基因包括 TaPIMP1、RD22、TLP4 和 PR1a,它们受 ABA 和水杨酸(SA)的调节。在 ABA 和 SA 处理后,TaPIMP1 低表达的转基因小麦显示这些应激响应基因的诱导能力受损。总之,TaPIMP1 作为一个正分子连接子,通过调节小麦 ABA 和 SA 信号通路中的应激相关基因,介导对禾旋孢腔菌和干旱胁迫的抗性。此外,TaPIMP1 可能为小麦的多抗性工程提供一种转基因工具。