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A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes

BACKGROUND: Plant protoplasts, a proven physiological and versatile cell system, are widely used in high-throughput analysis and functional characterization of genes. Green protoplasts have been successfully used in investigations of plant signal transduction pathways related to hormones, metabolite...

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Autores principales: Zhang, Yang, Su, Jianbin, Duan, Shan, Ao, Ying, Dai, Jinran, Liu, Jun, Wang, Peng, Li, Yuge, Liu, Bing, Feng, Dongru, Wang, Jinfa, Wang, Hongbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203094/
https://www.ncbi.nlm.nih.gov/pubmed/21961694
http://dx.doi.org/10.1186/1746-4811-7-30
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author Zhang, Yang
Su, Jianbin
Duan, Shan
Ao, Ying
Dai, Jinran
Liu, Jun
Wang, Peng
Li, Yuge
Liu, Bing
Feng, Dongru
Wang, Jinfa
Wang, Hongbin
author_facet Zhang, Yang
Su, Jianbin
Duan, Shan
Ao, Ying
Dai, Jinran
Liu, Jun
Wang, Peng
Li, Yuge
Liu, Bing
Feng, Dongru
Wang, Jinfa
Wang, Hongbin
author_sort Zhang, Yang
collection PubMed
description BACKGROUND: Plant protoplasts, a proven physiological and versatile cell system, are widely used in high-throughput analysis and functional characterization of genes. Green protoplasts have been successfully used in investigations of plant signal transduction pathways related to hormones, metabolites and environmental challenges. In rice, protoplasts are commonly prepared from suspension cultured cells or etiolated seedlings, but only a few studies have explored the use of protoplasts from rice green tissue. RESULTS: Here, we report a simplified method for isolating protoplasts from normally cultivated young rice green tissue without the need for unnecessary chemicals and a vacuum device. Transfections of the generated protoplasts with plasmids of a wide range of sizes (4.5-13 kb) and co-transfections with multiple plasmids achieved impressively high efficiencies and allowed evaluations by 1) protein immunoblotting analysis, 2) subcellular localization assays, and 3) protein-protein interaction analysis by bimolecular fluorescence complementation (BiFC) and firefly luciferase complementation (FLC). Importantly, the rice green tissue protoplasts were photosynthetically active and sensitive to the retrograde plastid signaling inducer norflurazon (NF). Transient expression of the GFP-tagged light-related transcription factor OsGLK1 markedly upregulated transcript levels of the endogeneous photosynthetic genes OsLhcb1, OsLhcp, GADPH and RbcS, which were reduced to some extent by NF treatment in the rice green tissue protoplasts. CONCLUSIONS: We show here a simplified and highly efficient transient gene expression system using photosynthetically active rice green tissue protoplasts and its broad applications in protein immunoblot, localization and protein-protein interaction assays. These rice green tissue protoplasts will be particularly useful in studies of light/chloroplast-related processes.
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spelling pubmed-32030942011-10-28 A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes Zhang, Yang Su, Jianbin Duan, Shan Ao, Ying Dai, Jinran Liu, Jun Wang, Peng Li, Yuge Liu, Bing Feng, Dongru Wang, Jinfa Wang, Hongbin Plant Methods Methodology BACKGROUND: Plant protoplasts, a proven physiological and versatile cell system, are widely used in high-throughput analysis and functional characterization of genes. Green protoplasts have been successfully used in investigations of plant signal transduction pathways related to hormones, metabolites and environmental challenges. In rice, protoplasts are commonly prepared from suspension cultured cells or etiolated seedlings, but only a few studies have explored the use of protoplasts from rice green tissue. RESULTS: Here, we report a simplified method for isolating protoplasts from normally cultivated young rice green tissue without the need for unnecessary chemicals and a vacuum device. Transfections of the generated protoplasts with plasmids of a wide range of sizes (4.5-13 kb) and co-transfections with multiple plasmids achieved impressively high efficiencies and allowed evaluations by 1) protein immunoblotting analysis, 2) subcellular localization assays, and 3) protein-protein interaction analysis by bimolecular fluorescence complementation (BiFC) and firefly luciferase complementation (FLC). Importantly, the rice green tissue protoplasts were photosynthetically active and sensitive to the retrograde plastid signaling inducer norflurazon (NF). Transient expression of the GFP-tagged light-related transcription factor OsGLK1 markedly upregulated transcript levels of the endogeneous photosynthetic genes OsLhcb1, OsLhcp, GADPH and RbcS, which were reduced to some extent by NF treatment in the rice green tissue protoplasts. CONCLUSIONS: We show here a simplified and highly efficient transient gene expression system using photosynthetically active rice green tissue protoplasts and its broad applications in protein immunoblot, localization and protein-protein interaction assays. These rice green tissue protoplasts will be particularly useful in studies of light/chloroplast-related processes. BioMed Central 2011-09-30 /pmc/articles/PMC3203094/ /pubmed/21961694 http://dx.doi.org/10.1186/1746-4811-7-30 Text en Copyright ©2011 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Zhang, Yang
Su, Jianbin
Duan, Shan
Ao, Ying
Dai, Jinran
Liu, Jun
Wang, Peng
Li, Yuge
Liu, Bing
Feng, Dongru
Wang, Jinfa
Wang, Hongbin
A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title_full A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title_fullStr A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title_full_unstemmed A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title_short A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
title_sort highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203094/
https://www.ncbi.nlm.nih.gov/pubmed/21961694
http://dx.doi.org/10.1186/1746-4811-7-30
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