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DOI: 10.1055/s-0029-1186161
© Georg Thieme Verlag KG Stuttgart · New York
A Simplified Method for Identifying the Panax ginseng Cultivar Gumpoong Based on 26S rDNA
Publikationsverlauf
received June 6, 2009
revised July 29, 2009
accepted August 27, 2009
Publikationsdatum:
29. September 2009 (online)

Abstract
Molecular identification of Panax ginseng (Korean ginseng) cultivars is very important for their management. We have developed a simple and reliable method for specific identification of the superior cultivar “Gumpoong.” The 26S rDNA was targeted for our molecular analysis, and a single-nucleotide polymorphism (SNP) was identified between Gumpoong and the other cultivars within the sequence data. From this SNP site, a modified allele-specific primer and a novel primer set have been developed to identify the Gumpoong cultivar via multiplex PCR. The established multiplex PCR method was determined to be effective, and the SNP marker showed high specificity to Gumpoong. Therefore, the described method may serve as a useful tool for rapid selection of Gumpoong cultivar.
Key words
Panax ginseng - Araliaceae - Gumpoong cultivar - 26S rDNA - SNP - multiplex PCR
References
- 1 Helms S. Cancer prevention and therapeutics: Panax ginseng. Altern Med Rev. 2004; 9 259-274
- 2 Ma K H, Dixit A, Kim Y C, Lee D Y, Kim T S, Cho E G, Park Y J. Development and characterization of new microsatellite markers for ginseng (Panax ginseng C. A. Meyer). Conserv Genet. 2007; 8 1507-1509
- 3 Wang H T, Sun H, Kwon W S, Jin H Z, Yang D C. Molecular identification of the Korean ginseng cultivar “Chunpoong” using the mitochondrial nad7 intron 4 region. Mitochondrial DNA. 2009; 20 41-45
- 4 Lee S S, Lee J H, Ahn I O. Characteristics of new cultivars in Panax ginseng C.A. Meyer. Proc Ginseng Soc Conf. 2005; 18 3-18
- 5 In D S, Kim Y C, Bang K H, Chung J W, Kim O T, Hyun D Y, Cha S W, Kim T S, Seong N S. Genetic relationships of Panax species by RAPD and ISSR analysis. Korean J Med Crop Sci. 2005; 13 249-253
- 6 Bang K H, Lee S W, Hyun D Y, Cho J H, Cha S W, Seong N S, Huh M K. Molecular authentication and genetic polymorphism of Korean ginseng (Panax ginseng C. A. Meyer) by inter-simple sequence repeats (ISSRs) markers. J Life Sci. 2004; 14 425-428
- 7 Kim O T, Bang K H, In D S, Lee J W, Kim Y C, Shin Y S, Hyun D Y, Lee S S, Cha S W, Seong N S. Molecular authentication of ginseng cultivars by comparison of internal transcribed spacer and 5.8S rDNA sequences. Plant Biotechnol Rep. 2007; 1 163-167
- 8 Kim J, Jo B H, Lee K L, Yoon E S, Ryu G H, Chung K W. Identification of new microsatellite markers in Panax ginseng. Mol Cells. 2007; 24 60-68
-
9 Little S.
ARMS analysis of point mutations. Taylor GR Laboratory methods for the detection of mutations and polymorphisms in DNA. Boca Raton; CRC Press 1997: 45-51 - 10 Kuzoff R K, Sweere J A, Soltis D E, Soltis P S, Zimmer E A. The phylogenetic potential of entire 26S rDNA sequences in plants. Mol Biol Evol. 1998; 15 251-263
- 11 Thompson J D, Gibson T J, Plewniak F, Jeanmougin F, Higgins D G. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997; 25 4876-4882
- 12 Newton C R, Graham A, Heptinstall L E, Powell S J, Summers C, Kalsheker N, Smith J C, Markham A F. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res. 1989; 17 2503-2516
- 13 Kwok S, Chang S Y, Sninsky J J, Wang A. A guide to the design and use of mismatched and degenerate primers. PCR Methods Appl. 1994; 3 S39-S47
Prof. Dr. Deok-Chun Yang
Korean Ginseng Center for Most Valuable Products &
Ginseng Genetic Resource Bank
Kyung Hee University
Yongin
446–701 Gyunggi-do
Republic of Korea
Telefon: + 82 3 12 01 26 88
Fax: + 82 3 12 02 26 87
eMail: deokchunyang@yahoo.co.kr