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High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes

BACKGROUND: Manipulation of the amylose-amylopectin ratio in cereal starch has been identified as a major target for the production of starches with novel functional properties. In wheat, silencing of starch branching enzyme genes by a transgenic approach reportedly caused an increase of amylose con...

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Autores principales: Botticella, Ermelinda, Sestili, Francesco, Hernandez-Lopez, Antonio, Phillips, Andrew, Lafiandra, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228712/
https://www.ncbi.nlm.nih.gov/pubmed/22074448
http://dx.doi.org/10.1186/1471-2229-11-156
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author Botticella, Ermelinda
Sestili, Francesco
Hernandez-Lopez, Antonio
Phillips, Andrew
Lafiandra, Domenico
author_facet Botticella, Ermelinda
Sestili, Francesco
Hernandez-Lopez, Antonio
Phillips, Andrew
Lafiandra, Domenico
author_sort Botticella, Ermelinda
collection PubMed
description BACKGROUND: Manipulation of the amylose-amylopectin ratio in cereal starch has been identified as a major target for the production of starches with novel functional properties. In wheat, silencing of starch branching enzyme genes by a transgenic approach reportedly caused an increase of amylose content up to 70% of total starch, exhibiting novel and interesting nutritional characteristics. In this work, the functionality of starch branching enzyme IIa (SBEIIa) has been targeted in bread wheat by TILLING. An EMS-mutagenised wheat population has been screened using High Resolution Melting of PCR products to identify functional SNPs in the three homoeologous genes encoding the target enzyme in the hexaploid genome. RESULTS: This analysis resulted in the identification of 56, 14 and 53 new allelic variants respectively for SBEIIa-A, SBEIIa-B and SBEIIa-D. The effects of the mutations on protein structure and functionality were evaluated by a bioinformatic approach. Two putative null alleles containing non-sense or splice site mutations were identified for each of the three homoeologous SBEIIa genes; qRT-PCR analysis showed a significant decrease of their gene expression and resulted in increased amylose content. Pyramiding of different single null homoeologous allowed to isolate double null mutants showing an increase of amylose content up to 21% compared to the control. CONCLUSION: TILLING has successfully been used to generate novel alleles for SBEIIa genes known to control amylose content in wheat. Single and double null SBEIIa genotypes have been found to show a significant increase in amylose content.
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spelling pubmed-32287122011-12-02 High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes Botticella, Ermelinda Sestili, Francesco Hernandez-Lopez, Antonio Phillips, Andrew Lafiandra, Domenico BMC Plant Biol Research Article BACKGROUND: Manipulation of the amylose-amylopectin ratio in cereal starch has been identified as a major target for the production of starches with novel functional properties. In wheat, silencing of starch branching enzyme genes by a transgenic approach reportedly caused an increase of amylose content up to 70% of total starch, exhibiting novel and interesting nutritional characteristics. In this work, the functionality of starch branching enzyme IIa (SBEIIa) has been targeted in bread wheat by TILLING. An EMS-mutagenised wheat population has been screened using High Resolution Melting of PCR products to identify functional SNPs in the three homoeologous genes encoding the target enzyme in the hexaploid genome. RESULTS: This analysis resulted in the identification of 56, 14 and 53 new allelic variants respectively for SBEIIa-A, SBEIIa-B and SBEIIa-D. The effects of the mutations on protein structure and functionality were evaluated by a bioinformatic approach. Two putative null alleles containing non-sense or splice site mutations were identified for each of the three homoeologous SBEIIa genes; qRT-PCR analysis showed a significant decrease of their gene expression and resulted in increased amylose content. Pyramiding of different single null homoeologous allowed to isolate double null mutants showing an increase of amylose content up to 21% compared to the control. CONCLUSION: TILLING has successfully been used to generate novel alleles for SBEIIa genes known to control amylose content in wheat. Single and double null SBEIIa genotypes have been found to show a significant increase in amylose content. BioMed Central 2011-11-10 /pmc/articles/PMC3228712/ /pubmed/22074448 http://dx.doi.org/10.1186/1471-2229-11-156 Text en Copyright ©2011 Botticella 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 Research Article
Botticella, Ermelinda
Sestili, Francesco
Hernandez-Lopez, Antonio
Phillips, Andrew
Lafiandra, Domenico
High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title_full High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title_fullStr High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title_full_unstemmed High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title_short High resolution melting analysis for the detection of EMS induced mutations in wheat SbeIIa genes
title_sort high resolution melting analysis for the detection of ems induced mutations in wheat sbeiia genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228712/
https://www.ncbi.nlm.nih.gov/pubmed/22074448
http://dx.doi.org/10.1186/1471-2229-11-156
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