4.3 Article

Transient gene expression system in zoysiagrass leaf mesophyll protoplasts

期刊

PLANT BIOTECHNOLOGY REPORTS
卷 16, 期 1, 页码 113-121

出版社

SPRINGER
DOI: 10.1007/s11816-021-00726-w

关键词

Protoplast; Transient expression; Polyethylene glycol; Zoysiagrass; Zoysia japonica

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2019R1A6A1A11052070, 2020R1I1A1A01057891, 2018R1C1B5086056, 2021R1A2C1012991]
  2. National Research Foundation of Korea [2018R1C1B5086056, 2020R1I1A1A01057891, 2021R1A2C1012991] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Transient expression of genes in zoysiagrass protoplasts is a valuable tool for rapidly investigating gene function and improving economic value through genetic manipulation. The technique shows high transfection efficiency and feasibility for cellular, biochemical, and molecular analyses in zoysiagrass protoplasts, providing insights for identifying valuable genes in Z. japonica or related species.
Transient expression of genes in protoplasts is a versatile technique for rapid functional characterization of genes by assessing protein localization or effector-reporter responses. In addition, protoplasts have been widely used for generating transgenic or gene-edited plants in model or crop plants. Zoysiagrass (Zoysia japonica Steud.) is one of the most economically important turf plants used in many living places or natural fields, but its management is labor-intensive. Therefore, genetic manipulation using valuable genes is highly demanded in zoysiagrass. Although transient expression systems in zoysiagrass facilitates the identification of valuable zoysiagrass genes, transient expression use in the zoysiagrass protoplasts is yet to be reported. Here we describe the methodology and feasibility for transient expression of genes in the zoysiagrass protoplasts isolated from green leaves. We obtained more than 70% of transfection efficiency in the zoysiagrass protoplasts using polyethylene glycol-mediated transfection. Additionally, we showed the feasibility of cellular, biochemical, and molecular approaches using the zoysiagrass protoplasts transiently expressing genes of interest through fluorescent microscopic observation, immunoblot analysis, and luciferase-based promoter activity assay. Along with the genome draft of the Zoysia family, transient expression will be a valuable tool to rapidly investigate gene functions. An initial assessment of gene function using protoplasts facilitate the identification of valuable genes that can improve the economic value of the Z. japonica or its closely related species by gene manipulation.

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