Cluster analysis of Chinese Hedychium based on SRAP markers

被引:3
作者
Gao, Li-Xia [2 ]
Hu, Xiu [2 ]
Liu, Nian [1 ]
Huang, Bang-Hai [3 ]
Li, Zheng-Jun [4 ]
Li, Yan [4 ]
机构
[1] Zhongkai Univ Agr & Technol, Guangzhou 510225, Guangdong, Peoples R China
[2] Chinese Acad Sci, S China Bot Garden, Guangzhou 510650, Peoples R China
[3] Guangzhou Municipal Ctr Promot Agr Technol, Guangzhou 510520, Guangdong, Peoples R China
[4] Zaozhuang Agr Technol Extens Ctr, Zaozhuang 277100, Shandong, Peoples R China
关键词
China; Cluster analysis; Hedychium; SRAP;
D O I
10.3724/SP.J.1002.2008.08012
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The traditional taxonomy of Hedychium was based on the bracts arrangement, imbricate or tubular, and this genus was divided into two subgenera. However, that was queried in recent years. The phylogenetic relationship of a total of 22 samples representing 19 species and I variety of Hedychium was investigated using SRAP technique. SRAP analysis produced 152 bands by using the 28 most informative primer pairs, 135 (88.8%) of which were polymorphic. Clustering analysis indicated that: (1) Hedychium from China can be divided into three groups. Plants in group I are short and distributed in limestone. Plants in group II are tall and seldom distributed in limestone. Plants in group III are with only one flower per bract, while plants in other two groups are with two or more flowers per bract. This result supports Wood's subdivision based on internal transcribed spacer sequence. (2) Wu's treatment by reducing H. emeiense Z. Y. Zhu to be a synonym of H. flavescens is supported. (3) H. flavum Roxb. and H. panzhuum Z. Y. Zhu are shown to be the same species, and H. panzhuum is reduced to be a synonym of H. flavum (4) The edaphic conditions are believed to be very important for the adaptation and evolution of Hedychium. In this paper, it is suggested that Hedychium be divided into two groups according to the number of flowers per bract.
引用
收藏
页码:899 / 905
页数:7
相关论文
共 27 条
[11]  
[李隆云 LI Longyun], 2008, [中国中药杂志, China Journal of Chinese Materia Medica], V33, P117
[12]  
Li Yan, 2005, Acta Horticulturae Sinica, V32, P643
[13]  
Lin Zhong-Xu, 2004, Acta Genetica Sinica, V31, P622
[14]   RAPID ISOLATION OF HIGH MOLECULAR-WEIGHT PLANT DNA [J].
MURRAY, MG ;
THOMPSON, WF .
NUCLEIC ACIDS RESEARCH, 1980, 8 (19) :4321-4325
[15]   ITS sequence data support a single origin for North American Astereae (Asteraceae) and reflect deep geographic divisions in Aster s.L. [J].
Noyes, RD ;
Rieseberg, LH .
AMERICAN JOURNAL OF BOTANY, 1999, 86 (03) :398-412
[16]   Genetic diversity of oilseed Brassica napus inbred lines based on sequence-related amplified polymorphism and its relation to hybrid performance [J].
Riaz, A ;
Li, G ;
Quresh, Z ;
Swati, MS ;
Quiros, CF .
PLANT BREEDING, 2001, 120 (05) :411-415
[17]  
SCHUMANN K, 2004, PFLANZENREICH, P46
[18]  
Sneath P. H. A., 1973, NUMERICAL TAXONOMY
[19]   Analysis of genetic diversity in Ganoderma population with a novel molecular marker SRAP [J].
Sun, Shu-Jing ;
Gao, Wei ;
Lin, Shu-Qian ;
Zhu, Jian ;
Xie, Bao-Gui ;
Lin, Zhi-Bin .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2006, 72 (03) :537-543
[20]  
Tong Hao-wen, 1997, Acta Palaeontologica Sinica, V36, P387