Wang Guoming, Guo Zhihua, Wang Tengjiao, Wang Xueping, Qi Kaijie, Xuan Jiping, Gu Chao, Zhang Shaoling
Sanya Institute of Nanjing Agricultural University, State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Nanjing Agricultural University, Nanjing, 210095, China.
Jiangsu Engineering Research Center for Germplasm Innovation and Utilization of Pecan, Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing, 210014, China.
Mol Hortic. 2024 Nov 15;4(1):38. doi: 10.1186/s43897-024-00114-2.
The plant hormone ethylene is indispensable to the ripening of climacteric fruits. Although extensive studies have been conducted on ethylene signaling, the ethylene response factor (ERF)-mediated transcriptional regulation of ethylene biosynthesis in pear fruits remains to be fully elucidated. We here constructed, sequenced, and analyzed transcriptome libraries in ethephon-treated and 1-MCP-treated Cuiguan pear fruits. In total, 721 fruit ripening-associated differentially expressed genes were identified. Among them, two key genes exhibited positive correlations: the 1-aminocyclopropane-1-carboxylic acid synthase (ACS)-encoding gene PbrACS3 and the ERF-encoding gene named PbrERF114. PbrERF114 overexpression increased ethylene production as well as the PbrACS3 expression level. Conversely, virus-induced gene silencing downregulated PbrERF114, thereby decreasing ethylene production and reducing PbrACS3 expression levels. Notably, PbrERF114 could directly interact with PbrACS3 and PbrERF24 promoters, thus inducing their expression. However, it did not result in an enhancement in luciferase activity, which is regulated by the PbrACS1b or PbrACO1 promoter. PbrERF24 could directly bind to PbrACO1 as well as PbrACS3 to promote ethylene synthesis. In conclusion, PbrERF114 can directly and indirectly mediate ethylene biosynthesis by transcriptionally regulating PbrACS3 and PbrERF24, respectively, thereby triggering a signaling cascade that induces the expression of both PbrACS3 and PbrACO1.
植物激素乙烯对于跃变型果实的成熟至关重要。尽管已对乙烯信号传导进行了广泛研究,但梨果实中乙烯反应因子(ERF)介导的乙烯生物合成转录调控仍有待充分阐明。我们在此构建、测序并分析了乙烯利处理和1-甲基环丙烯(1-MCP)处理的翠冠梨果实的转录组文库。总共鉴定出721个与果实成熟相关的差异表达基因。其中,两个关键基因呈现正相关:编码1-氨基环丙烷-1-羧酸合酶(ACS)的基因PbrACS3和编码ERF的基因PbrERF114。PbrERF114过表达增加了乙烯产量以及PbrACS3的表达水平。相反,病毒诱导的基因沉默下调了PbrERF114,从而降低了乙烯产量并降低了PbrACS3的表达水平。值得注意的是,PbrERF114可直接与PbrACS3和PbrERF24启动子相互作用,从而诱导它们的表达。然而,这并未导致由PbrACS1b或PbrACO1启动子调控的荧光素酶活性增强。PbrERF24可直接与PbrACO1以及PbrACS3结合以促进乙烯合成。总之,PbrERF114可分别通过转录调控PbrACS3和PbrERF24直接和间接介导乙烯生物合成,从而触发诱导PbrACS3和PbrACO1表达的信号级联反应。