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Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”

BACKGROUND: Korean ginseng (Panax ginseng) is a well-known medicinal plant of Oriental medicine that is still in practice today. Until now, a total of 11 Korean ginseng cultivars with unique features to Korean ginseng have been developed based on the pure-line-selection method. Among them, a new cul...

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Autores principales: Yang, Dong-Uk, Kim, Min-Kyeoung, Mohanan, Padmanaban, Mathiyalagan, Ramya, Seo, Kwang-Hoon, Kwon, Woo-Saeng, Yang, Deok-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223065/
https://www.ncbi.nlm.nih.gov/pubmed/28123319
http://dx.doi.org/10.1016/j.jgr.2015.12.007
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author Yang, Dong-Uk
Kim, Min-Kyeoung
Mohanan, Padmanaban
Mathiyalagan, Ramya
Seo, Kwang-Hoon
Kwon, Woo-Saeng
Yang, Deok-Chun
author_facet Yang, Dong-Uk
Kim, Min-Kyeoung
Mohanan, Padmanaban
Mathiyalagan, Ramya
Seo, Kwang-Hoon
Kwon, Woo-Saeng
Yang, Deok-Chun
author_sort Yang, Dong-Uk
collection PubMed
description BACKGROUND: Korean ginseng (Panax ginseng) is a well-known medicinal plant of Oriental medicine that is still in practice today. Until now, a total of 11 Korean ginseng cultivars with unique features to Korean ginseng have been developed based on the pure-line-selection method. Among them, a new cultivar namely G-1 with different agricultural traits related to yield and content of ginsenosides, was developed in 2012. METHODS: The aim of this study was to distinguish the new ginseng cultivar G-1 by identifying the unique single-nucleotide polymorphism (SNP) at its 45S ribosomal DNA and Panax quinquefolius region than other Korean ginseng cultivars using multiplex amplification-refractory mutation system–polymerase chain reaction (ARMS-PCR). RESULTS: A SNP at position of 45S ribosomal DNA region between G-1, P. quinquefolius, and the other Korean ginseng cultivars was identified. By designing modified allele-specific primers based on this site, we could specifically identified G-1 and P. quinquefolius via multiplex PCR. The unique primer for the SNP yielded an amplicon of size 449 bp in G-1 cultivar and P. quinquefolius. This study presents an effective method for the genetic identification of the G-1 cultivar and P. quinquefolius. CONCLUSION: The results from our study shows that this SNP-based approach to identify the G-1 cultivar will be a good way to distinguish accurately the G-1 cultivar and P. quinquefolius from other Korean ginseng cultivars using a SNP at 45S ribosomal DNA region.
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spelling pubmed-52230652017-01-25 Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1” Yang, Dong-Uk Kim, Min-Kyeoung Mohanan, Padmanaban Mathiyalagan, Ramya Seo, Kwang-Hoon Kwon, Woo-Saeng Yang, Deok-Chun J Ginseng Res Research Article BACKGROUND: Korean ginseng (Panax ginseng) is a well-known medicinal plant of Oriental medicine that is still in practice today. Until now, a total of 11 Korean ginseng cultivars with unique features to Korean ginseng have been developed based on the pure-line-selection method. Among them, a new cultivar namely G-1 with different agricultural traits related to yield and content of ginsenosides, was developed in 2012. METHODS: The aim of this study was to distinguish the new ginseng cultivar G-1 by identifying the unique single-nucleotide polymorphism (SNP) at its 45S ribosomal DNA and Panax quinquefolius region than other Korean ginseng cultivars using multiplex amplification-refractory mutation system–polymerase chain reaction (ARMS-PCR). RESULTS: A SNP at position of 45S ribosomal DNA region between G-1, P. quinquefolius, and the other Korean ginseng cultivars was identified. By designing modified allele-specific primers based on this site, we could specifically identified G-1 and P. quinquefolius via multiplex PCR. The unique primer for the SNP yielded an amplicon of size 449 bp in G-1 cultivar and P. quinquefolius. This study presents an effective method for the genetic identification of the G-1 cultivar and P. quinquefolius. CONCLUSION: The results from our study shows that this SNP-based approach to identify the G-1 cultivar will be a good way to distinguish accurately the G-1 cultivar and P. quinquefolius from other Korean ginseng cultivars using a SNP at 45S ribosomal DNA region. Elsevier 2017-01 2015-12-21 /pmc/articles/PMC5223065/ /pubmed/28123319 http://dx.doi.org/10.1016/j.jgr.2015.12.007 Text en Copyright © 2016, The Korean Society of Ginseng, Published by Elsevier. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Yang, Dong-Uk
Kim, Min-Kyeoung
Mohanan, Padmanaban
Mathiyalagan, Ramya
Seo, Kwang-Hoon
Kwon, Woo-Saeng
Yang, Deok-Chun
Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title_full Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title_fullStr Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title_full_unstemmed Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title_short Development of a single-nucleotide-polymorphism marker for specific authentication of Korean ginseng (Panax ginseng Meyer) new cultivar “G-1”
title_sort development of a single-nucleotide-polymorphism marker for specific authentication of korean ginseng (panax ginseng meyer) new cultivar “g-1”
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223065/
https://www.ncbi.nlm.nih.gov/pubmed/28123319
http://dx.doi.org/10.1016/j.jgr.2015.12.007
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