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Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina

The lack of a robust gene transformation tool that allows proper expression of foreign genes and functional testing for the vast number of nuclear genes in dinoflagellates has greatly hampered our understanding of the fundamental biology in this ecologically important and evolutionarily unique linea...

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Autores principales: Sprecher, Brittany N., Zhang, Huan, Lin, Senjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022241/
https://www.ncbi.nlm.nih.gov/pubmed/31963386
http://dx.doi.org/10.3390/microorganisms8010126
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author Sprecher, Brittany N.
Zhang, Huan
Lin, Senjie
author_facet Sprecher, Brittany N.
Zhang, Huan
Lin, Senjie
author_sort Sprecher, Brittany N.
collection PubMed
description The lack of a robust gene transformation tool that allows proper expression of foreign genes and functional testing for the vast number of nuclear genes in dinoflagellates has greatly hampered our understanding of the fundamental biology in this ecologically important and evolutionarily unique lineage of microeukaryotes. Here, we report the development of a dinoflagellate expression vector containing various DNA elements from phylogenetically separate dinoflagellate lineages, an electroporation protocol, and successful expression of introduced genes in an early branching dinoflagellate, Oxyrrhis marina. This protocol, involving the use of Lonza’s Nucleofector and a codon-optimized antibiotic resistance gene, has been successfully used to produce consistent results in several independent experiments for O. marina. It is anticipated that this protocol will be adaptable for other dinoflagellates and will allow characterization of many novel dinoflagellate genes.
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spelling pubmed-70222412020-03-09 Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina Sprecher, Brittany N. Zhang, Huan Lin, Senjie Microorganisms Article The lack of a robust gene transformation tool that allows proper expression of foreign genes and functional testing for the vast number of nuclear genes in dinoflagellates has greatly hampered our understanding of the fundamental biology in this ecologically important and evolutionarily unique lineage of microeukaryotes. Here, we report the development of a dinoflagellate expression vector containing various DNA elements from phylogenetically separate dinoflagellate lineages, an electroporation protocol, and successful expression of introduced genes in an early branching dinoflagellate, Oxyrrhis marina. This protocol, involving the use of Lonza’s Nucleofector and a codon-optimized antibiotic resistance gene, has been successfully used to produce consistent results in several independent experiments for O. marina. It is anticipated that this protocol will be adaptable for other dinoflagellates and will allow characterization of many novel dinoflagellate genes. MDPI 2020-01-16 /pmc/articles/PMC7022241/ /pubmed/31963386 http://dx.doi.org/10.3390/microorganisms8010126 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sprecher, Brittany N.
Zhang, Huan
Lin, Senjie
Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title_full Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title_fullStr Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title_full_unstemmed Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title_short Nuclear Gene Transformation in the Dinoflagellate Oxyrrhis marina
title_sort nuclear gene transformation in the dinoflagellate oxyrrhis marina
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7022241/
https://www.ncbi.nlm.nih.gov/pubmed/31963386
http://dx.doi.org/10.3390/microorganisms8010126
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