College of Biological and Environmental Sciences, Zhejiang Wanli University, Ningbo, Zhejiang, 315100, China.
Key Laboratory of Plant Molecular Physiology, CAS Center for Excellence in Molecular Plant Sciences, Institute of Botany, Chinese Academy of Sciences, Beijing, 10093, China.
Plant Physiol Biochem. 2022 Sep 1;186:11-18. doi: 10.1016/j.plaphy.2022.06.026. Epub 2022 Jul 1.
Apple (Malus domestica Borkh.) is not only an important fruit crop distributed worldwide, but also a common model plant. However, the lack of efficient genetic transformation procedures for apples limits the in-depth studies of their gene functions. Although leaf-regenerated adventitious shoots (LRAS) are a prerequisite for successful genetic transformation of apple, little is known about the underlying molecular mechanism of LRAS. Here, we identified the WUSCHEL-related homeobox (WOX) transcription factor in apple, MdWOX4-2, which was a transcriptional activator. Gene expression as well as morphological and histological observations revealed that MdWOX4-2 is involved in the development of LRAS. Overexpression of MdWOX4-2 conferred higher regenerative capacity in transgenic tobacco (Nicotiana tabacum) as compared to the wild type (WT). The combined results of the yeast one-hybrid (Y1H), electrophoretic mobility shift assay (EMSA), dual luciferase assays, and transient transactivation assay, revealed that MdWOX4-2 directly bound to and activated the MdLBD41 promoter. Moreover, transgenic experiments further demonstrated that MdLBD41 could significantly enhance the formation of adventitious shoot in transgenic tobacco. Collectively, our findings demonstrate that MdWOX4-2 is important for regulating the LRAS development by activating MdLBD41.
苹果(Malus domestica Borkh.)不仅是一种重要的水果作物,分布广泛,也是一种常见的模式植物。然而,苹果缺乏高效的遗传转化程序,限制了对其基因功能的深入研究。虽然叶片再生不定芽(LRAS)是苹果成功遗传转化的前提条件,但对于 LRAS 的潜在分子机制知之甚少。在这里,我们鉴定了苹果中的 WUSCHEL 相关同源盒(WOX)转录因子 MdWOX4-2,它是一种转录激活因子。基因表达以及形态和组织学观察表明,MdWOX4-2 参与了 LRAS 的发育。与野生型(WT)相比,过表达 MdWOX4-2 可赋予转基因烟草(Nicotiana tabacum)更高的再生能力。酵母单杂交(Y1H)、电泳迁移率变动分析(EMSA)、双荧光素酶报告基因分析和瞬时转激活分析的综合结果表明,MdWOX4-2 直接结合并激活 MdLBD41 启动子。此外,转基因实验进一步表明,MdLBD41 可显著增强转基因烟草中不定芽的形成。综上所述,我们的研究结果表明,MdWOX4-2 通过激活 MdLBD41 对调节 LRAS 发育具有重要作用。