生物技术通报 ›› 2016, Vol. 32 ›› Issue (4): 159-167.doi: 10.13560/j.cnki.biotech.bull.1985.2016.04.021

• 研究报告 • 上一篇    下一篇

滇杨遗传多样性的SRAP分析

颜璐茜1，2,李佳蔓1，2,员涛1，2,周安佩1，2,纵丹1，2,李旦3,辛培尧1，2，4,何承忠1，2，4   

  1. 1. 西南林业大学 云南省高校林木遗传改良与繁育重点实验室，昆明 650224;
    2. 西南林业大学 西南地区生物多样性保育国家林业局重点实验室，昆明 650224;
    3. 西南林业大学 云南生物多样性研究院，昆明 650224;
    4. 西南林业大学 西南山地森林资源保育与利用省部共建教育部重点实验室，昆明 650224
  • 收稿日期:2015-04-22 出版日期:2016-04-25 发布日期:2016-04-26
  • 作者简介:颜璐茜，女，硕士研究生，研究方向：植物生物技术；E-mail：695253285@qq.com
  • 基金资助:
    国家林业公益性行业专项（201104076），国家自然科学基金项目（31360184，31460205），云南省中青年学术与技术带头人后备人才培养基金项目（2012HB021），西南林业大学大学生创新基金项目（C14113）

Genetic Diversity Analysis of Populus yunnanensis by SRAP Markers

YAN Lu-xi1，2, LI Jia-man1，2, YUAN Tao1，2 ,ZHOU An-pei1，2 ,ZONG Dan1，2, LI Dan3, XIN Pei-yao1，2，4 ,HE Cheng-zhong1，2，4   

  1. 1. Key Laboratory for Forest Genetic and Tree Improvement & Propagation in Universities of Yunnan Province，Southwest Forestry University，Kunming 650224;
    2. Key Laboratory of Biodiversity Conservation in Southwest China，State Forestry Administration，Southwest Forestry University，Kunming 650224;
    3. Yunnan Academy of Biodiversity，Southwest Forestry University，Kunming 650224;
    4. Key Laboratory for Forest Resources Conservation and Use in the Southwest Mountains of China，Ministry of Education，Southwest Forestry University， Kunming 650224
  • Received:2015-04-22 Published:2016-04-25 Online:2016-04-26

PDF (PC)

339

摘要： 采用SRAP标记分析滇杨的遗传多样性和遗传结构。用筛选出的7对引物组合分析来自7个居群共208个样本，共扩增得到条带146条，多态性条带73条，多态带百分率为50%。滇杨物种水平上的观测等位基因数（Na）为1.500 0，有效等位基因数（Ne）为1.230 9，Nei’s基因多样性指数（H）与Shannon’s信息指数（I）分别为0.136 6与0.210 0。遗传分化系数（Gst）为0.529 4，基因流（Nm）为0.444 4，表明居群间的遗传变异大于居群内，其基因交流处于中等水平。AMOVA分析也表明居群间的变异占总变异的55.61%。UPGMA、PCoA和Bayesian聚类分析结果一致，均显示丽江与曲靖居群、楚雄与昭通居群的亲缘关系较近。Mantel test结果表明滇杨居群间的遗传距离与地理距离不相关。

关键词: 滇杨, 遗传多样性, 遗传结构, SRAP标记

Abstract: To figure out the genetic diversity and genetic structure of Populus yunnanensis，208 samples from 7 populations were analyzed by sequence-related amplified polymorphism（SRAP）markers. With selected 7 pairs of primers，146 bands were obtained，in which 73 fragments（50%）were polymorphic. The values at the species level were 1.500 0 for observed alleles number（Na），1.230 9 for effective alleles number（Ne），0.136 6 for Nei’s genetic diversity index（H），and 0.210 0 for Shannon’s information index（I）. The genetic differentiation coefficient（Gst）was 0.529 4 and gene flow（Nm）was 0.444 4 and on intermediate stage，indicating that genetic variability of P. yunnanensis mainly took place among populations. Similarly，AMOVA showed that the genetic diversity among populations accounted for 55.61% of total. Clustering analysis by UPGMA，PCoA and Bayesian constantly revealed that population Lijiang and Qujing were in close relationship，and the same for population Chuxiong and Zhaotong. In addition，no correlation between the genetic distance and geographical distance was found by Mantel Test.

Key words: Populus yunnanensis, genetic diversity, genetic structure, SRAP marker

网站版权 © 《生物技术通报》编辑部
地址：北京市中关村南大街12号　邮编：100081
电话：86-010-82109925, 82109903　 Email：biotech@caas.cn
本系统由北京玛格泰克科技发展有限公司设计开发