Development of a Specific SNP Marker to Identify the Medicinal Plants P. grandiflorum
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초록
The balloon flower (Platycodon grandiflorum A. DC.) is a medicinal and perennial flowering plant. Jangback is an important white-flowertype balloon flower cultivar registered in South Korea, but no molecular marker was available to differentiate it from other white-flowerlines. Therefore, we evaluated five P. grandiflorum white-flower lines and identified a single nucleotide polymorphism (SNP) derivedfrom the chloroplast TrnL-F genomic sequence that specifically differentiated Jangback from the other four genotypes. Cultivar identificationwas achieved by detecting allelic variations of the SNP using amplification refractory mutation system-polymerase chain reaction(ARMS-PCR) analysis and high resolution melting (HRM) curve analysis. The present study describes a rapid and reliable method toauthenticate the medicinally and economically valuable white-flower Jangback cultivar. Our results indicate that the plastid TrnL-F regionprovides for marker assisted identification and selection in intraspecific polymorphism studies, thereby the identified SNP marker providesa robust tool along with ARMS-PCR and HRM curve analysis for rapid and efficient identification of the medicinally valuable Jangbackcultivar.
Abstract
The balloon flower (Platycodon grandiflorum A. DC.) is a medicinal and perennial flowering plant. Jangback is an important white-flowertype balloon flower cultivar registered in South Korea, but no molecular marker was available to differentiate it from other white-flowerlines. Therefore, we evaluated five P. grandiflorum white-flower lines and identified a single nucleotide polymorphism (SNP) derivedfrom the chloroplast TrnL-F genomic sequence that specifically differentiated Jangback from the other four genotypes. Cultivar identificationwas achieved by detecting allelic variations of the SNP using amplification refractory mutation system-polymerase chain reaction(ARMS-PCR) analysis and high resolution melting (HRM) curve analysis. The present study describes a rapid and reliable method toauthenticate the medicinally and economically valuable white-flower Jangback cultivar. Our results indicate that the plastid TrnL-F regionprovides for marker assisted identification and selection in intraspecific polymorphism studies, thereby the identified SNP marker providesa robust tool along with ARMS-PCR and HRM curve analysis for rapid and efficient identification of the medicinally valuable Jangbackcultivar.
참고문헌 (20)
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