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Analysis of Population Structure and Genetic Diversity in Balloon Flower (Platycodon grandiflorum (Jacq.) A. DC.) Germplasm Using Simple Sequence Repeat (SSR) Markers
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  • Analysis of Population Structure and Genetic Diversity in Balloon Flower (Platycodon grandiflorum (Jacq.) A. DC.) Germplasm Using Simple Sequence Repeat (SSR) Markers
  • Analysis of Population Structure and Genetic Diversity in Balloon Flower (Platycodon grandiflorum (Jacq.) A. DC.) Germplasm Using Simple Sequence Repeat (SSR) Markers
저자명
Lee. Gi-An,Song. Jae Young,Sung. Jung Suk,Choi. Yu-Mi,Lee. Jung-Ro,Lee. Sok-Young,Kim. Chang-Yung,Kim. Yeon-Gyu,Lee. Myung-Chul
간행물명
Journal of crop science and biotechnology
권/호정보
2012년|15권 4호|pp.281-287 (7 pages)
발행정보
한국작물학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Balloon flower (Platycodon grandiflorum A. DC) is widely distributed in South Korea and there are some local landraces that are cultivated as a vegetable crop or medicinal plant. Making use of the gene resources of wild-type and landraces is a way to increase the genetic diversity of the cultivars. However, few tools or information are available on an efficient identification system for maintaining and management of these landraces. To improve the genetic resources for balloon flower, 22 simple sequence repeat (SSR) markers, also known as microsatellite markers, were evaluated in a collection of 42 balloon flower landraces, 34 of which were from Korea and eight from China. All microsatellite markers produced the 107 alleles ranging from 2 to 10 with a mean of 4.864 alleles per each locus ($N_A$). The values of observed heterozygosity ($H_O$) and expected heterozygosity ($H_E$) ranged from 0.00 to 0.667 (mean of 0.285) and from 0.024 to 0.741 (mean of 0.416), respectively. An average value of polymorphic information contents (PIC) were 0.382 with a range of 0.023 to 0.703. Results of population structure and phylogenetic and principal coordinate analysis (PCoA) indicated that P. grandiflorum germplasm formed two largely distinct clusters according to their origins and the genetic differentiation. There was a high level of genotypic diversity at broad geographic regions between Korea and China, but the low genetic differentiation was found within the collections from Korea. The results of the genetic diversity will be useful for the selection of the parents for developing balloon flower breeding and the multi-locus SSR markers developed herein will be a valuable resource for germplasm assessments, evaluation of genetic diversity, and population genetic studies of balloon flower.