The Engineering Research Institute of Agriculture and Forestry, Ludong University, 186 Hongqizhong Road, Yantai, Shandong 264025, China; The Key Laboratory of Molecular Module-Based Breeding of High Yield and Abiotic Resistant Plants in the Universities of Shandong, Ludong University, 186 Hongqizhong Road, Yantai 264025, China.
Taishan Academy of Forestry Sciences, Luohanya Road, Taian, Shandong 27100, China.
Plant Sci. 2025 Jan;350:112277. doi: 10.1016/j.plantsci.2024.112277. Epub 2024 Oct 9.
R2R3-MYB transcription factors function as the master regulators of the phenylpropanoid pathway in which both lignin and anthocyanin are produced. In poplar, R2R3-MYB transcription factor PdMYB118 positively regulates anthocyanin production to change leaf color. However, the molecular mechanism by which it controls different branches of the phenylpropanoid pathway still remains poorly understood. Here, we reported that in addition to anthocyanin synthesis, lignin deposition and xylem differentiation were regulated by PdMYB118 through inhibiting PagKNAT2/6b gene expression. The transgenic poplar plants overexpressing PdMYB118 accumulated more xylem, lignin and anthocyanin. Transcriptome and reverse transcription quantitative PCR analyses revealed that the expression of PagKNAT2/6b gene which inhibited lignin deposition and xylem differentiation was significantly down-regulated in transgenic poplar plants. Subsequent dual-luciferase reporter and yeast-one-hybrid assays demonstrated that PdMYB118 directly inhibited the transcription of PagKNAT2/6b by binding to the AC elements in its promoter region. Further experiments with transgenic poplar plants overexpressing PagKNAT2/6b demonstrated that overexpression of PagKNAT2/6b in the PdMYB118 overexpression background rescued lignin accumulation and xylem width to the same level of wild type plants. The findings in this work suggest that PdMYB118 is involved in the lignin deposition and xylem differentiation via modulating the expression of PagKNAT2/6b, and the PdMYB118- PagKNAT2/6b model can be used for the genetic breeding of new woody tree with high lignin production.
R2R3-MYB 转录因子作为苯丙烷途径的主调控因子,该途径既能合成木质素,也能合成花青素。在杨树中,R2R3-MYB 转录因子 PdMYB118 正向调控花青素的合成,从而改变叶片颜色。然而,其控制苯丙烷途径不同分支的分子机制仍知之甚少。本研究报道,除了花青素合成外,PdMYB118 通过抑制 PagKNAT2/6b 基因的表达来调节木质素的沉积和木质部的分化。过表达 PdMYB118 的转基因杨树积累了更多的木质部、木质素和花青素。转录组和反转录定量 PCR 分析表明,抑制木质素沉积和木质部分化的 PagKNAT2/6b 基因的表达在转基因杨树中显著下调。随后的双荧光素酶报告基因和酵母单杂交实验表明,PdMYB118 通过结合其启动子区的 AC 元件,直接抑制 PagKNAT2/6b 的转录。用过表达 PagKNAT2/6b 的转基因杨树进行的进一步实验表明,在 PdMYB118 过表达背景下过表达 PagKNAT2/6b 可将木质素积累和木质部宽度恢复到野生型植株的同一水平。本研究结果表明,PdMYB118 通过调节 PagKNAT2/6b 的表达参与木质素沉积和木质部分化,PdMYB118-PagKNAT2/6b 模型可用于遗传培育具有高木质素产量的新木本植物。