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Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products
BACKGROUND: Waxy-grain sorghum is used in most of the commercial cereal products in Korea. Worldwide, three waxy mutant alleles have been identified in the sorghum germplasm, and DNA markers for these alleles have been developed to identify the waxy genotype. However, that detection method cannot be...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372279/ https://www.ncbi.nlm.nih.gov/pubmed/25879964 http://dx.doi.org/10.1186/s12896-015-0134-z |
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author | Cho, Jaemin Jung, Taewook Kim, Jungin Song, Seokbo Ko, Jeeyeon Woo, Koansik Lee, Jaesaeng Choe, Myeongeun Oh, Inseok |
author_facet | Cho, Jaemin Jung, Taewook Kim, Jungin Song, Seokbo Ko, Jeeyeon Woo, Koansik Lee, Jaesaeng Choe, Myeongeun Oh, Inseok |
author_sort | Cho, Jaemin |
collection | PubMed |
description | BACKGROUND: Waxy-grain sorghum is used in most of the commercial cereal products in Korea. Worldwide, three waxy mutant alleles have been identified in the sorghum germplasm, and DNA markers for these alleles have been developed to identify the waxy genotype. However, that detection method cannot be used to determine the proportion of waxy content in samples containing both waxy and non-waxy sorghum. This study developed an assay that can be used to detect and quantify the waxy content of mixed cereal samples. RESULTS: All Korean waxy-grain sorghum used in this study contained the wx(a) allele, and one wx(a) allele-containing individual was also heterozygous for the wx(c) allele. No individuals possessed the wx(b) allele. The genotyping results were confirmed by iodine staining and amylose content analysis. Based on the sequence of the wx(a) allele, three different types of primers (wx(a) allele-specific, non-waxy allele-specific, and nonspecific) were designed for a quantitative real-time PCR (qPCR) assay; the primers were evaluated for qPCR using the following criteria: analytical specificity, sensitivity and repeatability. Use of this qPCR assay to analyze mixed cereal products demonstrated that it could accurately detect the waxy content of samples containing both waxy and non-waxy sorghum. CONCLUSIONS: We developed a qPCR assay to identify and quantify the waxy content of mixed waxy and non-waxy sorghum samples as well as mixtures of cereals including sorghum, rice and barley. The qPCR assay was highly specific; the allele-specific primers did not amplify PCR products from non-target templates. It was also highly sensitive, detecting a tiny amount (>0.5%) of waxy sorghum in the mixed samples; and it was simple and repeatable, implying the robust use of the assay. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-015-0134-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4372279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43722792015-03-25 Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products Cho, Jaemin Jung, Taewook Kim, Jungin Song, Seokbo Ko, Jeeyeon Woo, Koansik Lee, Jaesaeng Choe, Myeongeun Oh, Inseok BMC Biotechnol Research Article BACKGROUND: Waxy-grain sorghum is used in most of the commercial cereal products in Korea. Worldwide, three waxy mutant alleles have been identified in the sorghum germplasm, and DNA markers for these alleles have been developed to identify the waxy genotype. However, that detection method cannot be used to determine the proportion of waxy content in samples containing both waxy and non-waxy sorghum. This study developed an assay that can be used to detect and quantify the waxy content of mixed cereal samples. RESULTS: All Korean waxy-grain sorghum used in this study contained the wx(a) allele, and one wx(a) allele-containing individual was also heterozygous for the wx(c) allele. No individuals possessed the wx(b) allele. The genotyping results were confirmed by iodine staining and amylose content analysis. Based on the sequence of the wx(a) allele, three different types of primers (wx(a) allele-specific, non-waxy allele-specific, and nonspecific) were designed for a quantitative real-time PCR (qPCR) assay; the primers were evaluated for qPCR using the following criteria: analytical specificity, sensitivity and repeatability. Use of this qPCR assay to analyze mixed cereal products demonstrated that it could accurately detect the waxy content of samples containing both waxy and non-waxy sorghum. CONCLUSIONS: We developed a qPCR assay to identify and quantify the waxy content of mixed waxy and non-waxy sorghum samples as well as mixtures of cereals including sorghum, rice and barley. The qPCR assay was highly specific; the allele-specific primers did not amplify PCR products from non-target templates. It was also highly sensitive, detecting a tiny amount (>0.5%) of waxy sorghum in the mixed samples; and it was simple and repeatable, implying the robust use of the assay. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-015-0134-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-19 /pmc/articles/PMC4372279/ /pubmed/25879964 http://dx.doi.org/10.1186/s12896-015-0134-z Text en © Cho et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Cho, Jaemin Jung, Taewook Kim, Jungin Song, Seokbo Ko, Jeeyeon Woo, Koansik Lee, Jaesaeng Choe, Myeongeun Oh, Inseok Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title | Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title_full | Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title_fullStr | Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title_full_unstemmed | Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title_short | Development of a waxy gene real-time PCR assay for the quantification of sorghum waxy grain in mixed cereal products |
title_sort | development of a waxy gene real-time pcr assay for the quantification of sorghum waxy grain in mixed cereal products |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372279/ https://www.ncbi.nlm.nih.gov/pubmed/25879964 http://dx.doi.org/10.1186/s12896-015-0134-z |
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