Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha, 410205, China; Institute of Agriculture and Biotechnology, Hunan University of Humanities, Science and Technology, Loudi, 41700, China.
Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences, Changsha, 410205, China.
Biochem Biophys Res Commun. 2020 Oct 29;532(1):76-81. doi: 10.1016/j.bbrc.2020.07.073. Epub 2020 Aug 19.
Ethylene responsive factor ERF11 containing the ERF-associated amphiphilic repression (EAR) motif enhances plant resistance to bacterial pathogens. However, the underlying molecular mechanisms regulated by transcription factor ERF11 are poorly understood, in tobacco or other model plants. Here, we revealed the genome-wide binding landscape of BrERF11b in Nicotiana benthamian by conducting chromatin immunoprecipitation experiments followed by high-throughput sequencing (ChIP-seq) and bioinformatic analyses. Our results also revealed a GCCbox-like consensus BrERF11b-binding DNA motif: VCGCCGCC. By further integrative analysis of ChIP-seq and RNA-seq data, and the confirmation of electrophoretic mobility shift assay (EMSA), we screened three direct target genes NbNIMIN2, NbTAF15b and NbERF4. These results suggest that ERF11 may be involved in NPR1-mediated systemic acquired resistance (SAR), nucleotide-binding leucine-rich repeat immune receptors (NLR) -mediated autoimmunity, and HO generation, by direct transcriptional repression of NIM1-INTERACTING2 (NIMIN2), and transcriptional activation of TATA-binding protein-associated factor 15b (TAF15b) and ERF4. Our findings provide insightful information and valuable gene resource in unraveling the regulatory networks of plant defense responses to bacterial pathogens.
乙烯响应因子 ERF11 包含 ERF 相关的两亲性抑制(EAR)基序,可增强植物对细菌病原体的抗性。然而,在烟草或其他模式植物中,转录因子 ERF11 调控的潜在分子机制还知之甚少。在这里,我们通过染色质免疫沉淀实验(ChIP)结合高通量测序(ChIP-seq)和生物信息学分析,揭示了 BrERF11b 在 Nicotiana benthamiana 中的全基因组结合图谱。我们的研究结果还揭示了 BrERF11b 的一个 GCCbox 样保守结合 DNA 基序:VCGCCGCC。通过对 ChIP-seq 和 RNA-seq 数据的进一步综合分析,以及电泳迁移率变动分析(EMSA)的验证,我们筛选到三个直接靶基因 NbNIMIN2、NbTAF15b 和 NbERF4。这些结果表明,ERF11 可能通过直接转录抑制 NIM1-INTERACTING2(NIMIN2),以及转录激活 TATA 结合蛋白相关因子 15b(TAF15b)和 ERF4,参与 NPR1 介导的系统性获得抗性(SAR)、核苷酸结合富含亮氨酸重复免疫受体(NLR)介导的自身免疫以及 H2O2 的产生。我们的研究结果为解析植物防御反应对细菌病原体的调控网络提供了有价值的信息和基因资源。