A simplified method for identifying the Panax ginseng cultivar Gumpoong based on 26S rDNA.

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.

[1]  Deok-Chun Yang,et al.  Molecular identification of the Korean ginseng cultivar “Chunpoong” using the mitochondrial nad7 intron 4 region , 2009, Mitochondrial DNA.

[2]  Joonki Kim,et al.  Identification of new microsatellite markers in Panax ginseng. , 2007, Molecules and cells.

[3]  Young Chang Kim,et al.  Molecular authentication of ginseng cultivars by comparison of internal transcribed spacer and 5.8S rDNA sequences , 2007, Plant Biotechnology Reports.

[4]  Young-Chang Kim,et al.  Development and characterization of new microsatellite markers for ginseng (Panax ginseng C. A. Meyer) , 2007, Conservation Genetics.

[5]  Young-Chang Kim,et al.  Genetic Relationships of Panax Species by RAPD and ISSR Analyses , 2005 .

[6]  S. Helms Cancer prevention and therapeutics: Panax ginseng. , 2004, Alternative medicine review : a journal of clinical therapeutic.

[7]  허만규,et al.  Molecular Authentication and Genetic Polymorphism of Korean Ginseng (Panax ginseng C. A. Meyer) by Inter-Simple Sequence Repeats (ISSRs) Markers , 2004 .

[8]  Sung-Woo Lee,et al.  Molecular Authentication and Genetic Polymorphism of Korean Ginseng (Panax ginseng C. A. Meyer) by Inter-Simple Sequence Repeats (ISSRs) Markers , 2004 .

[9]  D. Soltis,et al.  The phylogenetic potential of entire 26S rDNA sequences in plants. , 1998, Molecular biology and evolution.

[10]  J. Thompson,et al.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.

[11]  S. Kwok,et al.  A guide to the design and use of mismatched and degenerate primers. , 1994, PCR methods and applications.

[12]  C Summers,et al.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). , 1989, Nucleic acids research.

[13]  J. Hafkenscheid,et al.  A Simplified Method , 1973 .

[14]  D J Moore,et al.  A simplified method of measuring the diameter of the anterior segment of the eye. , 1969, American journal of ophthalmology.