Integrative Biology Journals

Plant Diversity ›› 2007, Vol. 29 ›› Issue (06): 619-624.

• Articles • Previous Articles     Next Articles

Genetic Diversity of Jatropha curcas (Euphorbiaceae) Collected from Southern Yunnan, Detected by Inter-simple Sequence Repeat ( ISSR)

XIANG Zhen-Yong1 ,2 , 3 , SONG Song-Quan2 , WANG Gui-Juan2 ,
CHEN Mao-Sheng2 , YANG Cheng-Yuan2 , LONG Chun-Lin1   

  1. 1 Kunming Institute of Botany , Chinese Academy of Sciences , Kunming 650204 , China ;
    2 Xishuangbanna Tropical Botanical Garden , Chinese Academy of Sciences, Mengla 666303 , China ;
    3 College of Landscape and Horticulture , Yunnan Agriculture University , Kunming 650201 , China
  • Received:2007-04-12 Online:2007-12-25 Published:2007-12-25
  • Contact: LONG Chun-Lin

云南南部不同种源地小桐子遗传多样性的ISSR 分析

向振勇1 , 2 , 3 , 宋松泉2 , 王桂娟2 , 陈茂盛2 , 杨成源2 , 龙春林1   

  1. 1 中国科学院昆明植物研究所, 云南昆明 650204 ; 2 中国科学院西双版纳热带植物园, 云南勐腊 666303; 3 云南农业大学园林园艺学院, 云南昆明 650201
  • 通讯作者: 龙春林

Abstract:

The genetic diversity of 158 individuals from eight semi-wild populations from Yunnan Province was estimated using ISSR method (8 primers). The results revealed an extraordinarily high level of genetic diversity ( at species level,
percentage of polymorphic loci PPB = 91.04% , effective number of alleles Ne = 1.5244 , Nei′s (1973 ) gene diversity He= 0.3070, and Shannon′s information index Ho = 0 . 4618 ; at population level, PPB = 55. 04% , Ne = 1.3826, Nei′s (1973) gene diversity He = 0.2171, and Shannon′s information index Ho = 0.3178). The level of genetic differentiation between populations is lower than that among populations . The low level of genetic differentiation among populations was detected, based on Nei′s genetic diversity analysis (29.44%), and AMOVA (36.50%). There is no associations between geographical distance and genetic identity.We suggest that Jatropha curcas of Yunnan Province might not be introduced from the same place.

Key words: Jatropha curcas

摘要: 应用ISSR 分子标记方法对采自云南的8 个居群的小桐子( Jatropha curcas) 共158 个个体进行遗传多样性分析。8 个ISSR 引物共扩增到了67 个位点, 其中61 个是多态性位点。分析结果表明: (1) 云南小桐子的遗传多样性水平很高。在物种水平上, 平均每个位点的多态位点百分率PPB = 91.04% , 有效等位基因数Ne = 1.5244, Nei′s 基因多样性指数He= 0.3070, Shannon 多样性信息指数Ho = 0.4618; 在居群水平上, PPB = 55.04%, Ne = 1.3826, He = 0.2171, Shannon 多样性信息指数Ho = 0.3178。(2) 居群间的遗传分化低于居群内的遗传分化。基于Nei's 遗传多样性分析得出的居群间遗传多样性分化系数Gst = 0.2944。AMOVA分析显示: 云南小桐子的遗传变异主要存在于居群内, 占总变异的63.50%, 居群间的遗传变异占36.50%。(3) 居群间的地理距离及遗传一致度并不存在相关性。鉴于以上指标, 我们推测云南小桐子可能来自不同的地区。

关键词: 小桐子, 遗传变异, ISSR

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