Identification of Cymbidium spp. by randomly amplified polymorphic DNA markers

碩士 === 國立中興大學 === 園藝學系 === 85 === Morphological traits and randomly amplified polymorphic DNA (RAPD) markerswere used to study the identification and discrimination of Cymbidium species.The purposes of this study were to establish the m...

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Bibliographic Details
Main Authors: Chiou, Chin-Chun, 邱金春
Other Authors: Wang, Tsai-Yih, Tseng, Menq-Jaiu
Format: Others
Language:zh-TW
Published: 1997
Online Access:http://ndltd.ncl.edu.tw/handle/00190219285461565041
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Summary:碩士 === 國立中興大學 === 園藝學系 === 85 === Morphological traits and randomly amplified polymorphic DNA (RAPD) markerswere used to study the identification and discrimination of Cymbidium species.The purposes of this study were to establish the molecular markers for discrimination of the Cymbidium spp. and cultivars and to explore the relationships of genetic linkage among the Cymbidium spp. and cultivars. The data of phenotype characters and growth habit showed that the tenCymbidium spp. can be discriminated followed the order of serrulated marginof leaf, leaf shape, leaf size, and growth habit. However, fifteen cultivars ofCymbidium can only be parly discriminated with leaf stripes and leaf shape. Twenty DNA primers, which generated clear and discriminative polymorphicDNA fragments, were selected from 300 random primers to discriminate ten Cymbidium species. Of 79 polymorphic DNA fragments, 46 fragment were species-specific and 33 fragments were presented between two Cymbidium spp. Therewere averaged 12.5 amplified DNA fragments a-nd 3.9 DNA polymorphic markersgenerated by each primer. The results of linkagof cluster analysis revealedthat the ten Cymbidium spp. can be classified into four groups, the first group includes terrestrial plants of C. rubrigemmum, C. ensifolium var. misericors, C. karan, C. sinense and C.tortisepalum, the second group includes C. lancifolium form aspidistrifolium and C. formosanum, the third group includes epiphytic plants of C. Sensation and C. pumilumm, and the fourth group includes C. dayanum var. austro-japonicum with the lowest similar-ity with other Cymbidium spp. Eleven DNA primers were selected from 300 random primers to discriminate fifteen cultivars of Cymbidium. Of 21 polymorphic DNA fragments which discriminated eleven cultivars of Cymbidiu sinense, 11 fragments were cultivar-specific and 10 were shared among two to four cultivars. There were averaged 11 amplified DNA fragments and 1.9 DNA polymorphic markers gener-ated by each primer. The results of linkage cluster analysis revealed that the eleven cultivars of Cymbidium sinense can be classified into four groups, the first group includes C. sinense and `taur-ji', the second group includes `rueih-baau', `yarng-ming-jiin', `jin- shan', `shyueh-bair-jaau' and`shyuh-huarng', thethird group includes ` shyr-mern', and the fourth groupincludes `jin-huah- shan' and `shih-ba-hsiieh-shih'.