Abstract

Each plant cell has hundreds of copies of the chloroplast genome and chloroplast transgenes do not undergo silencing. Therefore, chloroplast transformation has many powerful potential agricultural and industrial applications. We previously succeeded in integrating exogenous genes into the chloroplast genome using peptide–DNA complexes composed of plasmid DNA and a fusion peptide consisting of a cell-penetrating peptide (CPP) and a chloroplast transit peptide (cpPD complex). However, how cpPD complexes are transported into the chloroplast from outside the cell remains unclear. Here, to characterize the route by which these cpPD complexes move into chloroplasts, we tracked their movement from the extracellular space to the chloroplast stroma using a fluorescent label and confocal laser scanning microscopy (CLSM). Upon infiltration of cpPD complexes into the extracellular space of Arabidopsis thaliana leaves, the complexes reached the chloroplast surface within 6h. The cpPD complexes reached were engulfed by the chloroplast outer envelope membrane and gradually integrated into the chloroplast. We detected several cpPD complexes localized around chloroplast nucleoids and observed the release of DNA from the cpPD. Our results thus define the route taken by the cpPD complexes for gene delivery from the extracellular space to the chloroplast stroma.

Highlights

  • Chloroplasts have a small genome, the remnants of the endosymbiotic cyanobacterium genome

  • To understand how the peptide-pDNA complex is internalized into a cell and delivered to chloroplast nucleoids, we tracked the peptide-pDNA complex using imaging technology with the previously designed peptide, KH-AtOEP34 [protein sequence: (KH)-AtOEP34, and the plasmid PpsbA-aadA-sGFP-TpsbA (Yoshizumi et al, 2018)

  • Confocal microscopy analysis and the generation of full z-stack images revealed that cpPD-Cy3 complexes penetrate into cells and chloroplasts within 6 h after their infiltration into the extracellular space

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Summary

Introduction

Chloroplasts have a small genome, the remnants of the endosymbiotic cyanobacterium genome. The chloroplast genome has become an ideal bioengineering target to produce high-value commodities, such as vitamins, vaccines, as well as medical and agricultural compounds, at large scales (Verma et al, 2008; Maliga and Bock, 2011; Jin and Daniell, 2015; Adem et al, 2017). Several methods have been reported for chloroplast transformation in various plant species, such as polyethylene glycol (PEG) treatment of protoplasts or biolistic bombardment of leaves, suspension cell cultures, and embryogenic callus tissue (Golds et al, 1993; Svab and Maliga, 1993; Bock, 2015). Chloroplast transformation efficiency is low and a simple and efficient method that can be applied to various plant species would enable broad application of this technology

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