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Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes

BACKGROUND: Recently, an integrated DNA walking strategy has been proposed to prove the presence of GMO via the characterisation of sequences of interest, including their transgene flanking regions and the unnatural associations of elements in their transgenic cassettes. To this end, the p35S, tNOS...

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Autores principales: Fraiture, Marie-Alice, Vandamme, Julie, Herman, Philippe, Roosens, Nancy H. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020286/
https://www.ncbi.nlm.nih.gov/pubmed/29945581
http://dx.doi.org/10.1186/s12896-018-0446-x
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author Fraiture, Marie-Alice
Vandamme, Julie
Herman, Philippe
Roosens, Nancy H. C.
author_facet Fraiture, Marie-Alice
Vandamme, Julie
Herman, Philippe
Roosens, Nancy H. C.
author_sort Fraiture, Marie-Alice
collection PubMed
description BACKGROUND: Recently, an integrated DNA walking strategy has been proposed to prove the presence of GMO via the characterisation of sequences of interest, including their transgene flanking regions and the unnatural associations of elements in their transgenic cassettes. To this end, the p35S, tNOS and t35S pCAMBIA elements have been selected as key targets, allowing the coverage of most of GMO, EU authorized or not. In the present study, a bidirectional DNA walking method anchored on the CryAb/c genes is proposed with the aim to cover additional GMO and additional sequences of interest. RESULTS: The performance of the proposed bidirectional DNA walking method anchored on the CryAb/c genes has been evaluated in a first time for its feasibility using several GM events possessing these CryAb/c genes. Afterwards, its sensitivity has been investigated through low concentrations of targets (as low as 20 HGE). In addition, to illustrate its applicability, the entire workflow has been tested on a sample mimicking food/feed matrices analysed in GMO routine analysis. CONCLUSION: Given the successful assessment of its performance, the present bidirectional DNA walking method anchored on the CryAb/c genes can easily be implemented in GMO routine analysis by the enforcement laboratories and allows completing the entire DNA walking strategy in targeting an additional transgenic element frequently found in GMO. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-018-0446-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60202862018-07-06 Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes Fraiture, Marie-Alice Vandamme, Julie Herman, Philippe Roosens, Nancy H. C. BMC Biotechnol Research Article BACKGROUND: Recently, an integrated DNA walking strategy has been proposed to prove the presence of GMO via the characterisation of sequences of interest, including their transgene flanking regions and the unnatural associations of elements in their transgenic cassettes. To this end, the p35S, tNOS and t35S pCAMBIA elements have been selected as key targets, allowing the coverage of most of GMO, EU authorized or not. In the present study, a bidirectional DNA walking method anchored on the CryAb/c genes is proposed with the aim to cover additional GMO and additional sequences of interest. RESULTS: The performance of the proposed bidirectional DNA walking method anchored on the CryAb/c genes has been evaluated in a first time for its feasibility using several GM events possessing these CryAb/c genes. Afterwards, its sensitivity has been investigated through low concentrations of targets (as low as 20 HGE). In addition, to illustrate its applicability, the entire workflow has been tested on a sample mimicking food/feed matrices analysed in GMO routine analysis. CONCLUSION: Given the successful assessment of its performance, the present bidirectional DNA walking method anchored on the CryAb/c genes can easily be implemented in GMO routine analysis by the enforcement laboratories and allows completing the entire DNA walking strategy in targeting an additional transgenic element frequently found in GMO. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-018-0446-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-27 /pmc/articles/PMC6020286/ /pubmed/29945581 http://dx.doi.org/10.1186/s12896-018-0446-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fraiture, Marie-Alice
Vandamme, Julie
Herman, Philippe
Roosens, Nancy H. C.
Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title_full Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title_fullStr Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title_full_unstemmed Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title_short Development and validation of an integrated DNA walking strategy to detect GMO expressing cry genes
title_sort development and validation of an integrated dna walking strategy to detect gmo expressing cry genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020286/
https://www.ncbi.nlm.nih.gov/pubmed/29945581
http://dx.doi.org/10.1186/s12896-018-0446-x
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