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两个大珠母贝群体遗传多样性的ISSR分析 被引量:13

ISSR analysis of genetic diversity in two populations of pearl oyster Pinctada maxima
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摘要 用ISSR标记技术对我国两个大珠母贝Pinctada maxima群体的遗传多样性进行分析。7条ISSR引物在两个群体中共得到91个清晰的扩增位点。总多态位点百分率为100%,H=0.2832,I=0.4372,总的遗传变异中有21.54%的变异存在于两个群体之间,而78.46%的遗传变异是发生在群体内。海南群体的遗传多样性水平(PPB=91.21%,I=0.4144±0.2364,H=0.2715±0.1790)高于广西群体(PPB=82.42%,I=0.3621±0.2534,H=0.2356±0.1837),广西群体的单态位点数(15个)明显高于海南群体(8个)。NJ聚类分析表明两群体各自聚类成一簇。研究结果表明我国大珠母贝的遗传多样性水平较高。 Genetic diversity within and between two geographical populations of Pinctada maxima from Hainan and Guangxi provinces in China was determined using inter simple sequence repeats (ISSR). Seven primers produced 91 bands across a total of 80 individuals. The genetic diversity was high at species level (PPB = 100%, H = 0. 283 2, and I = 0. 437 2), 21.54% of the total genetic variation resided between the two populations and 78.46% within the populations. Higher genetic diversity level was observed in the Hainan population (PPB = 91.21%, H = 0. 271 5, and I = 0. 414 4) compared with the Guangxi population (PPB = 82.42%, H = 0. 235 6, and I = 0. 362 1); however, the number of monomorphic sites of the Guangxi population (15) was greater than that of the Hainan population (8). NJ Cluster analysis divided the populations into two main groups. The results of this study suggested that there is a higher genetic diversity level in P. maxima populations in China and greater genetic variation between the Guangxi and Hainan populations.
出处 《热带海洋学报》 CAS CSCD 北大核心 2008年第3期61-65,共5页 Journal of Tropical Oceanography
基金 "863"项目(2002AA603022) 中国科学院南海海洋研究所创新项目(LYQY200316)
关键词 大珠母贝Pinctada MAXIMA 遗传多样性 ISSR Pinctada maxima genetic diversity ISSR
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参考文献14

  • 1ROSE R A, BAKER S B. Larval and spat culture of the western Australian silver-or gold-lip pearl oyster, Pinctada maxima Jameson (Mollusca: Pteriidae) [J]. Aquaculture, 1994, 126:35-50.
  • 2TAYLOR J J, SOUTHGATE P C, ROBERT R A, et al. Assessment of artificial substrates for collection of hatcheryreared silver lip pearl oyster (Pinctada maxima, Jameson) spat[J]. Aquaculture, 1998, 152:219-230.
  • 3邓陈茂,梁飞龙,符韶.大珠母贝人工苗养成的研究[J].海洋科学,2000,24(10):11-13. 被引量:28
  • 4JOHNSON M S, JOLL L M. Genetic subdivision of the pearl oyster Pinctada maxima (Jameson, 1901) (Mollusca: Pteriidae) in northern Australian [J]. Freshwater Res, 1993, 44:519- 526.
  • 5BENZIE J A, SMITH C, SUGAMA K, et al. Mitochondrial DNA reveals genetic differentiation between Australian and Indonesian pearl oyster Pinctada maxima (Jameson1901) populations[J]. J Shellfish Res, 2003, 22 (3): 781- 787.
  • 6SMITH C, BENZIE J A H, WILSON K J. Isolation and characterization of eight microsatellite loci from silver- lipped pearl oyster Pinctada maxima [J ]. Molecular Ecology Notes, 2003, 3 (1): 125 -127.
  • 7RATNAPARKHE M B, TEKEOGLU M, MUEHLBAUER F J. Inter-simple-sequence repeat (ISSR) polymorphisms are useful for finding markers associated with disease resistance gene elusters[J].Theor Appl Genet, 1998, 98: 515- 519.
  • 8MATTIONAI C, CASASOLI M, GONZALEZ M, et al. Comparison of ISSR and RAPD markers to characterize three Chilean Nothofagus species[J]. Theor Appl Genet, 2002, 104: 1064-1070.
  • 9ADAMS R P, SCHWARZBACH A E, PANDEY R N. The concordance of tetraploid, ISSR and RAPD markers, and ITS sequence data sets among genotypes: an example from Juniperus[J]. Biochem Systematics and Ecol, 2003, 31: 375-387.
  • 10谢佳燕,张知彬.ISSR标记技术及其在遗传多样性研究中的应用[J].兽类学报,2004,24(1):71-77. 被引量:38

二级参考文献22

  • 1权洁霞.梭鱼和中国对虾的遗传多样性以及对虾总科12种虾的分子系统进化.青岛海洋大学博士论文[M].,2000..
  • 2Smith P L, Gaffney PM, Purves M. Genetic markers for identification of Patagonian and toothfish, Journal of Fish,2001,58:1 190-1 194.
  • 3Gustine D L, Voigt P W, Brummer C, et al. Genetic variation of RAPD markers for Narth American white clover collections and cultivars. Crop Sci, 2002,42:343-347.
  • 4Burr K, Harper R, Linacre A. One-step isolation of plant DNA suitable for PCR amplification. Plant Molecular Biology Reporter, 2001, 19:367-371.
  • 5Steiner J J ,Poklemba C J ,Jellstrom, et al. A rapid one-tube genomic DNA extraction process for PCR and RAPD analyses Nucleic Acids Research, 1995, 23(13) : 2 569-2 570.
  • 6Apostol B L, Black IV W C, Reiter P, et al. Population genetics with RAPD-PCR markers: the breeding structure of Aedes aegypti in Puerto Rico[J]. Heredity, 1996, 76:325-334.
  • 7Lynch M.. The similarity index and DNA fingerprinting[J]. Mol Biol Evol, 1990, 7:478-484.
  • 8Wachirs F N, Waugh R, Hackett C A. Detection of genetic in tea (Camellia sinensis) using RAPD makers[J].Genome, 1995,38:201-210.
  • 9蒙钊美,珍珠养殖理论与技术,1996年,33页
  • 10谢玉坎,珍珠科学,1995年,37页

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