Transcription factor PdMYB118 in poplar regulates lignin deposition and xylem differentiation in addition to anthocyanin synthesis through suppressing the expression of PagKNAT2/6b gene

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Plant Science Pub Date : 2024-10-09 DOI:10.1016/j.plantsci.2024.112277
Shuo Song , Wei Guo , Yu Guo , Erkun Chao , Sujie Sun , Lizi Zhao , Yanqiu Zhao , Hongxia Zhang
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Abstract

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.
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杨树中的转录因子 PdMYB118 除了通过抑制 PagKNAT2/6b 基因的表达来调节木质素沉积和木质部分化外,还能调节花青素的合成。
R2R3-MYB 转录因子是产生木质素和花青素的苯丙酮途径的主调节因子。在杨树中,R2R3-MYB 转录因子 PdMYB118 能正向调节花青素的产生,从而改变叶片颜色。然而,人们对其控制苯丙酮途径不同分支的分子机制仍然知之甚少。在此,我们报道了 PdMYB118 除了调控花青素的合成外,还通过抑制 PagKNAT2/6b 基因的表达来调控木质素的沉积和木质部的分化。过表达 PdMYB118 的转基因杨树植株积累了更多的木质部、木质素和花青素。转录组和逆转录定量 PCR 分析表明,在转基因杨树植株中,抑制木质素沉积和木质部分化的 PagKNAT2/6b 基因表达显著下调。随后进行的双荧光素酶报告和酵母一杂交试验表明,PdMYB118 通过与 PagKNAT2/6b 启动子区域中的 AC 元件结合,直接抑制了 PagKNAT2/6b 的转录。用过表达 PagKNAT2/6b 的转基因杨树植株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与野生型植株相同的水平。该研究结果表明,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模型可用于遗传育种高木质素产量的新型木本植物。
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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