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A high-efficiency transient expression system mediated by Agrobacterium tumefaciens in Spinacia oleracea leaves

文献类型： 外文期刊

作者： Zhang, Yumeng 1 ; Qiu, Liuliu 1 ; Zhang, Yongxue 1 ; Wang, Yiran 1 ; Fu, Chunxiang 3 ; Dai, Shaojun 1 ; Sun, Meihong 1 ;

作者机构： 1.Shanghai Normal Univ, Coll Life Sci, Dev Ctr Plant Germplasm Resources, Shanghai 200234, Peoples R China

2.Shanghai Acad Agr Sci, Hort Res Inst, Shanghai Key Lab Protected Hort Technol, Shanghai 201403, Peoples R China

3.Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Shandong Technol Innovat Ctr Synthet Biol, Shandong Prov Key Lab Energy Genet, Qingdao 266000, Peoples R China

关键词： Transient gene expression; Spinach; Subcellular localization; Protein-protein interaction

期刊名称：PLANT METHODS （ 影响因子：4.7； 五年影响因子：5.6 ）

ISSN：

年卷期： 2024 年 20 卷 1 期

页码：

收录情况： SCI

摘要： Background Optimization of a highly efficient transient expression system is critical for the study of gene function, particularly in those plants in which stable transformation methods are not widely available. Agrobacterium tumefaciens-mediated transient transformation is a simple and low-cost method that has been developed and applied to a wide variety of plant species. However, the transient expression in spinach (Spinacia oleracea L.) is still not reported. Results We developed a transient expression system in spinach leaves of the Sp75 and Sp73 varieties. Several factors influencing the transformation efficiency were optimized such as Agrobacterium strain, spinach seedling stage, leaf position, and the expression time after injection. Agrobacterium strain GV3101 (pSoup-p19) was more efficient than AGL1 in expressing recombinant protein in spinach leaves. In general, Sp75 leaves were more suitable than Sp73 leaves, regardless of grow stage. At four-leaf stage, higher intensity and efficiency of transient expression were observed in group 1 (G1) of Sp75 at 53 h after injection (HAI) and in G1 of Sp73 at 64 HAI. At six-leaf stage of Sp75, group 3 (G3) at 72 HAI were the most effective condition for transient expression. Using the optimized expression system, we detected the subcellular localization of a transcriptional co-activator SoMBF1c and a NADPH oxidase SoRbohF. We also detected the interaction of the protein kinase SoCRK10 and the NADPH oxidase SoRbohB. Conclusion This study established a method of highly efficient transient expression mediated by Agrobacterium in spinach leaves. The transient expression system will facilitate the analysis of gene function and lay a solid foundation for molecular design breeding of spinach.

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