Matsuo Naoki, Banno Hiroharu
Plant Biology Research Center, Chubu University, Kasugai, Aichi 487-8501, Japan.
Plant Physiol Biochem. 2008 Dec;46(12):1045-50. doi: 10.1016/j.plaphy.2008.07.007. Epub 2008 Jul 25.
The Arabidopsis Enhancer of Shoot Regeneration 1 (ESR1) gene regulates initiation of in vitro shoot regeneration. In this study, we investigated the transcription-modulating potential of ESR1. ESR1 induced reporter gene expression when overexpressed transiently in Arabidopsis leaf cells. Experiments using a fusion protein with the GAL4 DNA-binding domain located a transactivating domain of ESR1 within the C-terminal region. A nuclear localization signal was also located within the AP2/ERF domain. These results demonstrated that ESR1 functions as a transcriptional activator. Furthermore, we examined whether transcriptional modulation by ESR1 affects the in vitro shoot regeneration efficiency. Overexpression of ESR1 fused with the VP16 transactivating domain enhanced in vitro shoot regeneration as well as overexpressed wild-type ESR1 did, while overexpression of ESR1 fused with a strong repression domain, SRDX, inhibited shoot regeneration. These results suggest that ESR1 induces shoot regeneration through its transactivating ability.
拟南芥茎再生增强子1(ESR1)基因调控体外茎再生的起始。在本研究中,我们研究了ESR1的转录调控潜力。ESR1在拟南芥叶细胞中瞬时过表达时可诱导报告基因表达。使用与GAL4 DNA结合结构域融合的蛋白进行的实验将ESR1的反式激活结构域定位在C末端区域内。核定位信号也位于AP2/ERF结构域内。这些结果表明ESR1作为转录激活因子发挥作用。此外,我们研究了ESR1的转录调控是否影响体外茎再生效率。与VP16反式激活结构域融合的ESR1过表达与野生型ESR1过表达一样增强了体外茎再生,而与强抑制结构域SRDX融合的ESR1过表达则抑制了茎再生。这些结果表明ESR1通过其反式激活能力诱导茎再生。