Development of an EST-SSR marker in Panax ginseng

Cheng-jun Yang, W. Jun, Li-qiang Mu, Shao-Chen Li, GuanJun Liu, Chang-Qun Hu
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引用次数: 8

Abstract

A total of 791 microsatellites (SSRs) were isolated from 7055 Panax ginseng expressed sequence tags (ESTs). According to primer design criteria, 68 primer pairs for EST-SSR were designed. Under an appropriate polymerase chain reaction (PCR) system, all EST-SSR primer pairs were screened against genomic DNA of Ji'anchangbo and Fusong'ermaya from Panax ginseng , and 43 EST-SSR primer pairs out of the above 68 resulted in PCR products. Then, all 43 pairs were detected in nine P. ginseng , two Panax quinquefolius and two Acanthopanax senticosus cultivars for polymorphisms, and 26 pairs (60.47%) were found to be polymorphic, accounting for 38.23% of the total number of designed primer pairs. These results demonstrate the possibility of developing EST-SSR markers using P. ginseng ESTs.
人参EST-SSR标记的开发
从7055个人参表达序列标签(ESTs)中共分离到791个微卫星(SSRs)。根据引物设计标准,共设计了68对EST-SSR引物。采用合适的聚合酶链反应(PCR)系统对所有EST-SSR引物进行筛选,筛选出68对EST-SSR引物中43对为PCR产物。在9个人参、2个西洋参和2个刺五加品种中检测到全部43对引物的多态性,其中26对(60.47%)为多态性,占设计引物总数的38.23%。这些结果证明了利用人参ESTs开发EST-SSR标记的可能性。
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