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COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants
Advancing basic and applied plant research requires the continuous innovative development of the available technology toolbox. Essential components of this toolbox are methods that simplify the assembly, delivery, and expression of multiple transgenes of interest. To allow simultaneous and direction...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772762/ https://www.ncbi.nlm.nih.gov/pubmed/26973687 http://dx.doi.org/10.3389/fpls.2016.00246 |
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author | Ghareeb, Hassan Laukamm, Sabine Lipka, Volker |
author_facet | Ghareeb, Hassan Laukamm, Sabine Lipka, Volker |
author_sort | Ghareeb, Hassan |
collection | PubMed |
description | Advancing basic and applied plant research requires the continuous innovative development of the available technology toolbox. Essential components of this toolbox are methods that simplify the assembly, delivery, and expression of multiple transgenes of interest. To allow simultaneous and directional multigene assembly on the same plant transformation vector, several strategies based on overlapping sequences or restriction enzymes have recently been developed. However, the assembly of homologous and repetitive DNA sequences can be inefficient and the frequent occurrence of target sequences recognized by commonly used restriction enzymes can be a limiting factor. Here, we noted that recognition sites for the restriction enzyme SfiI are rarely occurring in plant genomes. This fact was exploited to establish a multigene assembly system called “COLORFUL-Circuit.” To this end, we developed a set of binary vectors which provide a flexible and cost efficient cloning platform. The gene expression cassettes in our system are flanked with unique SfiI sites, which allow simultaneous multi-gene cassette assembly in a hosting binary vector. We used COLORFUL-Circuit to transiently and stably express up to four fluorescent organelle markers in addition to a selectable marker and analyzed the impact of assembly design on coexpression efficiency. Finally, we demonstrate the utility of our optimized “COLORFUL-Circuit” system in an exemplary case study, in which we monitored simultaneously the subcellular behavior of multiple organelles in a biotrophic plant–microbe interaction by Confocal Laser Scanning Microscopy. |
format | Online Article Text |
id | pubmed-4772762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47727622016-03-11 COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants Ghareeb, Hassan Laukamm, Sabine Lipka, Volker Front Plant Sci Plant Science Advancing basic and applied plant research requires the continuous innovative development of the available technology toolbox. Essential components of this toolbox are methods that simplify the assembly, delivery, and expression of multiple transgenes of interest. To allow simultaneous and directional multigene assembly on the same plant transformation vector, several strategies based on overlapping sequences or restriction enzymes have recently been developed. However, the assembly of homologous and repetitive DNA sequences can be inefficient and the frequent occurrence of target sequences recognized by commonly used restriction enzymes can be a limiting factor. Here, we noted that recognition sites for the restriction enzyme SfiI are rarely occurring in plant genomes. This fact was exploited to establish a multigene assembly system called “COLORFUL-Circuit.” To this end, we developed a set of binary vectors which provide a flexible and cost efficient cloning platform. The gene expression cassettes in our system are flanked with unique SfiI sites, which allow simultaneous multi-gene cassette assembly in a hosting binary vector. We used COLORFUL-Circuit to transiently and stably express up to four fluorescent organelle markers in addition to a selectable marker and analyzed the impact of assembly design on coexpression efficiency. Finally, we demonstrate the utility of our optimized “COLORFUL-Circuit” system in an exemplary case study, in which we monitored simultaneously the subcellular behavior of multiple organelles in a biotrophic plant–microbe interaction by Confocal Laser Scanning Microscopy. Frontiers Media S.A. 2016-03-01 /pmc/articles/PMC4772762/ /pubmed/26973687 http://dx.doi.org/10.3389/fpls.2016.00246 Text en Copyright © 2016 Ghareeb, Laukamm and Lipka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Ghareeb, Hassan Laukamm, Sabine Lipka, Volker COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title | COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title_full | COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title_fullStr | COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title_full_unstemmed | COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title_short | COLORFUL-Circuit: A Platform for Rapid Multigene Assembly, Delivery, and Expression in Plants |
title_sort | colorful-circuit: a platform for rapid multigene assembly, delivery, and expression in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772762/ https://www.ncbi.nlm.nih.gov/pubmed/26973687 http://dx.doi.org/10.3389/fpls.2016.00246 |
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