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ISSR分析3种类型黄连的遗传多样性和遗传结构 被引量:2

Analysis on genetic diversity and genetic structure among three types of Coptis chinensis by ISSR
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摘要 目的研究3种类型黄连的遗传多样性和遗传结构。方法对3种类型黄连的90个单株进行ISSR分析,运用POPGENE 1.31软件计算相关参数。结果 22个引物共检测到164个位点,其中108个为多态位点;黄连3种类型具有较丰富的遗传多样性,在物种水平上,多态位点百分率(PPB)为65.85%,有效等位基因数(Ne)为1.229 8,Nei’s基因多样度指数(H)为0.144 0,物种水平Shannon’s多样性信息指数(Hsp)为0.230 2;在类型水平上,PPB为55.08%,Ne为1.218 9,H为0.136 0,类型水平Shannon’s多样性信息指数(Hpop)为0.215 1。Nei’s基因多样性指数计算的类型间遗传分化系数与Shannon’s类型分化系数分别为0.056 1和0.065 2,均说明大部分遗传变异存在于类型内;ISSR标记检测到类型间存在着广泛的基因流(Nm=8.405 4),遗传分化程度较低;两两类型间的Nei’s遗传一致度(I)的范围为0.983 1~0.989 7;根据Nei’s遗传距离进行各类型间的UPGMA聚类,基于ISSR分子标记的聚类结果与形态分类基本一致。结论 3种类型的黄连遗传多样性较高,为新品种的培育提供了丰富的遗传基础。 Objective To investigate the genetic diversity and genetic structure among three types of Coptis chinensis by ISSR. Methods Ninety individuals of the three types of C. chinensis were employed for inter-simple sequence repeat (ISSR) analysis. The parameters were calculated by POPGENE 1.31. Results A total of 164 bands were amplified by 22 primers, among which 108 were polymorphic; A relatively high level of genetic diversity was revealed at species level: PPB = 65.85%, Are = 1.229 8, H = 0.144 0, and Hsp = 0.230 2; while at type level, PPB = 55.08%, Ne = 1.218 9, H= 0.136 0, and Hpop = 0.215 1; The Nei's coefficient of genetic differentiation was 0.056 1, which was consistent with the Shannon's coefficient of genetic differentiation (0.065 2). Most of the genetic variation existed among types; The gene flow (Nm = 8.405 4) was high among cultivars, indicating that the degree of genetic differentiation was lower; Genetic similarity coefficient (I) changed from 0.983 1 to 0.989 7. By UPGMA clustering analysis and Nei's genetic distance, the cluster analysis based on ISSR and classification of morphology were almost the same. Conclusion The relatively high genetic diversity of C. chinensis provides the basis for breeding new varieties.
出处 《中草药》 CAS CSCD 北大核心 2012年第8期1595-1598,共4页 Chinese Traditional and Herbal Drugs
基金 国家科技重大专项资助项目(2009ZX09308-002 2012ZX09304006) 国家科技支撑计划资助项目(2011BAI13B02-1) 国家科技攻关计划资助项目(2004BA721A32)
关键词 黄连 遗传多样性 遗传结构 基因流 ISSR Coptis chinensis Franch. genetic diversity genetic structure gene flow ISSR
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  • 1孙红祥,张昌禧,吴远文.黄连属药用植物的数量分类学研究[J].中国药学杂志,1995,30(1):7-9. 被引量:3
  • 2朱强,王有为,齐海涛,王庆.不同品系黄连产量和质量的研究[J].中草药,2006,37(12):1866-1869. 被引量:12
  • 3胡娟:药用黄连的分子系统学和保护遗传学研究[D].2010.
  • 4Cai YF, Li SW, Chen M, etal. Molecular phyloge-ny of Ranunculaceae based on rbcL sequences[J]. Biologia, 2010, 65(6): 997.
  • 5Li R, Fan W, Tian G, et al. The sequence and de novo assembly of the giant panda genome[J]. Na- ture, 2010, 463(7279): 311.
  • 6Smith D R, Quinlan A R, Peckham H E, et al. Rapid whole-genome mutational profiling using next-generation sequencing technologies [ J ]. Ge- nome research, 2008, 18(10): 1638.
  • 7Cheung M S, Down T A, Latorre I, etal. System- atic bias in high-throughput sequencing data and its correction by BEADS[J]. Nucleic acids research, 2011, 39(15): el03.
  • 8Aird D, Ross M G, Chen W S, et al. Analyzing and minimizing PCR amplification bias in Iltumina sequencing libraries[J]. Genome biology, 2011, 12 (2) : R18.
  • 9Bentley D R, Balasubramanian S, Swerdlow H P, et al. Accurate whole human genome sequencing using reversible terminator chemistry[J]. Nature, 2008, 456(7218) : 53.
  • 10王翀,周天华,杨雪,郭晶,赵桂仿.ISSR-PCR鉴别绞股蓝属7种植物[J].中草药,2008,39(4):588-591. 被引量:23

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