Abstract

Green fluorescent protein (GFP) has been widely used for monitoring gene expression and protein localization in diverse organisms. However, highly sensitive imaging equipment, like fluorescence microscope, is usually required for the visualization of GFP, limitings its application to fixed locations in samples. A reporter that can be visualized in real-time regardless the shape, size and location of the target samples will increase the flexibility and efficiency of research work. Here, we report the application of a GFP-like protein, called eYGFPuv, in both transient expression and stable transformation, in two herbaceous plant species (Arabidopsis and tobacco) and two woody plant species (poplar and citrus). We observed bright fluorescence under UV light in all of the four plant species without any effects on plant growth or development. eYGFPuv was shown to be effective for imaging transient expression in leaf and root tissues. With a focus on in vitro transformation, we demonstrated that the transgenic events expressing 1x eYGFPuv could be easily identified visually during the callus stage and the shoot stage, enabling early and efficient selection of transformants. Furthermore, whole-plant level visualization of eYGFPuv revealed its ubiquitous stability in transgenic plants. In addition, our transformation experiments showed that eYGFPuv can also be used to select transgenic plants without antibiotics. This work demonstrates the feasibility of utilizing 1x eYGFPuv in studies of gene expression and plant transformation in diverse plants.

Highlights

  • Reporter genes and systems have been playing essential roles in biological sciences

  • In this study, we demonstrate that green fluorescence can be seen under UV light by naked eyes at both the tissue and the whole-plant level through transient gene expression and stable transformation of 1x eYGFPuv in herbaceous and woody plants

  • In the in vitro transformation, 1x eYGFPuv can be used as a selectable marker for in vivo selection of transformants through live imaging without the need for destructive sampling required by PCR-based genotyping or GUS staining, saving time and cost (Fig. 7A)

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Summary

Introduction

Various reporter genes have been developed and adapted to a diverse set of organisms, e.g., lacZ in microbes[1], β-glucuronidase (GUS) in plants[2], luciferase (LUC)[3] and green fluorescent protein (GFP)[4] in both prokaryotic and eukaryotic organisms, to name a few. Multiple GFPuv-related studies have been reported in plants, its applications have been limited. Agrobacterium-mediated in planta transformation and tissue-culture-based transformation are the most commonly used methods for plant genetic engineering[10,11,12,13]. One unavoidable issue related to tissue-culturebased transformation and in planta transformation with antibiotic resistance genes as selectable markers is falsepositive transformant shoots or escapees on selection media[14,15]. Efforts to eliminate falsepositive transformants, typically by using GUS assay and PCR analysis of target DNAs, have been deployed

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