Yusuf Ahmed, Wakaya Kota, Sakamoto Takuya, Uemura Takuya, Okamura Koudai, Ramadan Abdelaziz, Nozawa Akira, Suzuki Takamasa, Inui Yayoi, Matsunaga Sachihiro, Sawasaki Tatsuya, Arimura Gen-Ichiro
Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, Tokyo, Japan.
Department of Botany, Faculty of Science, Ain Shams University, Cairo, Egypt.
Plant Cell Environ. 2025 May;48(5):3257-3268. doi: 10.1111/pce.15345. Epub 2024 Dec 25.
Histone modification is a cellular process for transcriptional regulation. In herbivore-damaged plants, activation of genes involved in defence responses is required for antiherbivore properties, but little is known about how the chromatin remodelling system is involved. In Arabidopsis (Arabidopsis thaliana) plants responding to Spodoptera litura larvae, HAC1 and HDA6, a histone acetyltransferase and a histone deacetylase, respectively, were found here to be involved in histone H3 (Lys9; H3K9) acetylation/deacetylation at the promoter region of the plant defensin gene PDF1.2 and the gene body of ethylene response factor 13 (ERF13) as early as 2 h after the onset of herbivore attack. The H3K9 acetylation was responsible for the robust upregulation of PDF1.2 later, at 24 h, and ERF13 even earlier, at 1 h. TOPLESS (TPL) and TOPLESS-related (TPR) corepressors interacted with HDA6 to deacetylate H3K9 at PDF1.2 and ERF13, while negatively regulating the expression of PDF1.2 but not ERF13. Furthermore, TPL also interacted with ERF13, resulting in ERF13-mediated regulation of PDF1.2. Taken together, these data suggest a model of promoter-restricted, TPL/TPR-directed histone deacetylation and transcription factor repression in healthy Arabidopsis plants for the feedback regulation of the antiherbivore response.
组蛋白修饰是一种用于转录调控的细胞过程。在遭受食草动物损害的植物中,参与防御反应的基因激活是植物具备抗食草动物特性所必需的,但关于染色质重塑系统如何参与其中却知之甚少。在拟南芥植株对斜纹夜蛾幼虫作出反应的过程中,研究发现,早在食草动物攻击开始后2小时,组蛋白乙酰转移酶HAC1和组蛋白去乙酰化酶HDA6就参与了植物防御素基因PDF1.2启动子区域以及乙烯反应因子13(ERF13)基因体上组蛋白H3(赖氨酸9;H3K9)的乙酰化/去乙酰化过程。H3K9乙酰化在之后的24小时导致了PDF1.2的强烈上调,而在更早的1小时就导致了ERF13的上调。TOPLESS(TPL)和TOPLESS相关(TPR)共抑制因子与HDA6相互作用,使PDF1.2和ERF13上的H3K9去乙酰化,同时对PDF1.2的表达起负调控作用,但对ERF13不起作用。此外,TPL还与ERF13相互作用,导致ERF13介导对PDF1.2的调控。综上所述,这些数据表明,在健康的拟南芥植株中,存在一种启动子受限、TPL/TPR导向的组蛋白去乙酰化和转录因子抑制模型,用于抗食草动物反应的反馈调控。