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A simple and efficient method for isolating small RNAs from different plant species

BACKGROUND: Small RNAs emerged over the last decade as key regulators in diverse biological processes in eukaryotic organisms. To identify and study small RNAs, good and efficient protocols are necessary to isolate them, which sometimes may be challenging due to the composition of specific tissues o...

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Autores principales: Rosas-Cárdenas, Flor de Fátima, Durán-Figueroa, Noé, Vielle-Calzada, Jean-Philippe, Cruz-Hernández, Andrés, Marsch-Martínez, Nayelli, de Folter, Stefan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056851/
https://www.ncbi.nlm.nih.gov/pubmed/21349188
http://dx.doi.org/10.1186/1746-4811-7-4
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author Rosas-Cárdenas, Flor de Fátima
Durán-Figueroa, Noé
Vielle-Calzada, Jean-Philippe
Cruz-Hernández, Andrés
Marsch-Martínez, Nayelli
de Folter, Stefan
author_facet Rosas-Cárdenas, Flor de Fátima
Durán-Figueroa, Noé
Vielle-Calzada, Jean-Philippe
Cruz-Hernández, Andrés
Marsch-Martínez, Nayelli
de Folter, Stefan
author_sort Rosas-Cárdenas, Flor de Fátima
collection PubMed
description BACKGROUND: Small RNAs emerged over the last decade as key regulators in diverse biological processes in eukaryotic organisms. To identify and study small RNAs, good and efficient protocols are necessary to isolate them, which sometimes may be challenging due to the composition of specific tissues of certain plant species. Here we describe a simple and efficient method to isolate small RNAs from different plant species. RESULTS: We developed a simple and efficient method to isolate small RNAs from different plant species by first comparing different total RNA extraction protocols, followed by streamlining the best one, finally resulting in a small RNA extraction method that has no need of first total RNA extraction and is not based on the commercially available TRIzol(® )Reagent or columns. This small RNA extraction method not only works well for plant tissues with high polysaccharide content, like cactus, agave, banana, and tomato, but also for plant species like Arabidopsis or tobacco. Furthermore, the obtained small RNA samples were successfully used in northern blot assays. CONCLUSION: Here we provide a simple and efficient method to isolate small RNAs from different plant species, such as cactus, agave, banana, tomato, Arabidopsis, and tobacco, and the small RNAs from this simplified and low cost method is suitable for downstream handling like northern blot assays.
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spelling pubmed-30568512011-03-15 A simple and efficient method for isolating small RNAs from different plant species Rosas-Cárdenas, Flor de Fátima Durán-Figueroa, Noé Vielle-Calzada, Jean-Philippe Cruz-Hernández, Andrés Marsch-Martínez, Nayelli de Folter, Stefan Plant Methods Methodology BACKGROUND: Small RNAs emerged over the last decade as key regulators in diverse biological processes in eukaryotic organisms. To identify and study small RNAs, good and efficient protocols are necessary to isolate them, which sometimes may be challenging due to the composition of specific tissues of certain plant species. Here we describe a simple and efficient method to isolate small RNAs from different plant species. RESULTS: We developed a simple and efficient method to isolate small RNAs from different plant species by first comparing different total RNA extraction protocols, followed by streamlining the best one, finally resulting in a small RNA extraction method that has no need of first total RNA extraction and is not based on the commercially available TRIzol(® )Reagent or columns. This small RNA extraction method not only works well for plant tissues with high polysaccharide content, like cactus, agave, banana, and tomato, but also for plant species like Arabidopsis or tobacco. Furthermore, the obtained small RNA samples were successfully used in northern blot assays. CONCLUSION: Here we provide a simple and efficient method to isolate small RNAs from different plant species, such as cactus, agave, banana, tomato, Arabidopsis, and tobacco, and the small RNAs from this simplified and low cost method is suitable for downstream handling like northern blot assays. BioMed Central 2011-02-24 /pmc/articles/PMC3056851/ /pubmed/21349188 http://dx.doi.org/10.1186/1746-4811-7-4 Text en Copyright ©2011 Rosas-Cárdenas 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
Rosas-Cárdenas, Flor de Fátima
Durán-Figueroa, Noé
Vielle-Calzada, Jean-Philippe
Cruz-Hernández, Andrés
Marsch-Martínez, Nayelli
de Folter, Stefan
A simple and efficient method for isolating small RNAs from different plant species
title A simple and efficient method for isolating small RNAs from different plant species
title_full A simple and efficient method for isolating small RNAs from different plant species
title_fullStr A simple and efficient method for isolating small RNAs from different plant species
title_full_unstemmed A simple and efficient method for isolating small RNAs from different plant species
title_short A simple and efficient method for isolating small RNAs from different plant species
title_sort simple and efficient method for isolating small rnas from different plant species
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056851/
https://www.ncbi.nlm.nih.gov/pubmed/21349188
http://dx.doi.org/10.1186/1746-4811-7-4
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