State Key Laboratory of Plant Genomics, National Center for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, Innovation Academy of Seed Design, Chinese Academy of Sciences, Beijing 100101, China; CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Crop Biology, College of Horticulture Science and Engineering, Shandong Agricultural University, Tai'an 271018, China.
Mol Plant. 2022 Aug 1;15(8):1329-1346. doi: 10.1016/j.molp.2022.06.014. Epub 2022 Jul 3.
The plant hormone jasmonate (JA) regulates plant immunity and adaptive growth by orchestrating a genome-wide transcriptional program. Key regulators of JA-responsive gene expression include the master transcription factor MYC2, which is repressed by the conserved Groucho/Tup1-like corepressor TOPLESS (TPL) in the resting state. However, the mechanisms underlying TPL-mediated transcriptional repression of MYC2 activity and hormone-dependent switching between repression and de-repression remain enigmatic. Here, we report the regulation of TPL activity and JA signaling by reversible acetylation of TPL. We found that the histone acetyltransferase GCN5 could mediate TPL acetylation, which enhances its interaction with the NOVEL-INTERACTOR-OF-JAZ (NINJA) adaptor and promotes its recruitment to MYC2 target promoters, facilitating transcriptional repression. Conversely, TPL deacetylation by the histone deacetylase HDA6 weakens TPL-NINJA interaction and inhibits TPL recruitment to MYC2 target promoters, facilitating transcriptional activation. In the resting state, the opposing activities of GCN5 and HDA6 maintain TPL acetylation homeostasis, promoting transcriptional repression activity of TPL. In response to JA elicitation, HDA6 expression is transiently induced, resulted in decreased TPL acetylation and repressor activity, thereby transcriptional activation of MYC2 target genes. Thus, the GCN5-TPL-HDA6 module maintains the homeostasis of acetylated TPL, thereby determining the transcriptional state of JA-responsive genes. Our findings uncovered a mechanism by which the TPL corepressor activity in JA signaling is actively tuned in a rapid and reversible manner.
植物激素茉莉酸(JA)通过协调全基因组转录程序来调节植物的免疫和适应性生长。JA 响应基因表达的关键调节剂包括主转录因子 MYC2,在静止状态下,它被保守的 Groucho/Tup1 样共抑制因子 TOPLESS(TPL)抑制。然而,TPL 介导的 MYC2 活性转录抑制和激素依赖性抑制与去抑制之间转换的机制仍然神秘。在这里,我们报告了 TPL 活性和 JA 信号的调节通过 TPL 的可逆乙酰化来实现。我们发现组蛋白乙酰转移酶 GCN5 可以介导 TPL 乙酰化,这增强了它与 NOVEL-INTERACTOR-OF-JAZ(NINJA)接头的相互作用,并促进其募集到 MYC2 靶启动子,从而促进转录抑制。相反,组蛋白去乙酰化酶 HDA6 通过去乙酰化 TPL 削弱了 TPL-NINJA 相互作用,并抑制了 TPL 向 MYC2 靶启动子的募集,从而促进转录激活。在静止状态下,GCN5 和 HDA6 的相反活性维持 TPL 乙酰化的平衡,促进 TPL 的转录抑制活性。在响应 JA 诱导时,HDA6 的表达短暂诱导,导致 TPL 乙酰化和抑制活性降低,从而 MYC2 靶基因的转录激活。因此,GCN5-TPL-HDA6 模块维持了乙酰化 TPL 的平衡,从而决定了 JA 响应基因的转录状态。我们的发现揭示了一种机制,即 JA 信号中转录抑制因子 TPL 的活性以快速和可逆的方式被主动调节。