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  4. 蝴蝶蘭基因體研究計畫─以核糖體RNA基因為蝴蝶蘭屬植物的分子標誌
 
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蝴蝶蘭基因體研究計畫─以核糖體RNA基因為蝴蝶蘭屬植物的分子標誌

Date Issued
2005
Date
2005
Author(s)
高燕玉
DOI
922317B002021
URI
http://ntur.lib.ntu.edu.tw//handle/246246/5049
Abstract
18S-5.8S-26S (45S) and 5S rDNAs are organized into clusters of tandem repeat with each repeat consisting of a transcribed region, and an intergenic spacer (IGS). In the transcribed region of 45S rDNA, on either side of 5.8S rDNA are found internal transcribed spacers (ITS), described as ITS1 and ITS2. The ITS and IGS have sequences diverged more than the transcribed region, and the presence of highly conserved sequences flanking each of ITS and IGS make them easy to amplify and useful for phylogenetic analyses of interspecies. In this study, the IGS sequences of 28 Phalaenopsis species and one Doritis species were amplified by the polymerase chain reaction (PCR) which used specific primers devised by 5S rDNA transcribed region of P. aphrodite. The neighbor-joining tree constructed from IGS consensus sequences divides the 28 Phalaenopsis species into seven groups. The species from four groups coincided with the results from the IGS and ITS sequences analyses. Additionally, species in IGS phylogenetic tree were in agreement with traditional taxonomic status.
Subjects
Phalaenopsis
IGS
phylogeny
Publisher
臺北市:國立臺灣大學分子與細胞生物學研究所
Type
report
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922317B002021.pdf

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