长竹蛏不同地理居群的遗传多样性  

GENETIC DIVERSITY OF DIFFERENT GEOGRAPHICAL POPULATIONS IN SOLEN STRICTUS REVEALED BY ISSR MARKERS

作　　者：陈燕妮[1] 孙振兴[1] 常林瑞[1] 

机构地区：[1]鲁东大学生命科学学院,烟台264025

出　　处：《水生生物学报》2010年第2期270-277,共8页Acta Hydrobiologica Sinica

基　　金：山东省高校实验技术研究项目(2005-396)资助

摘　　要：研究以大连、烟台、莱州、青岛和赣榆近海5个不同地理居群的长竹蛏(Solen strictus Gould)为实验材料,利用ISSR分子标记进行了遗传多样性的研究。结果表明,13个ISSR引物在5个居群中共扩增出200个位点,平均每个引物记录15.4个位点,5个居群的多态位点比例为43.56%—60.43%。长竹蛏在物种水平上的Nei’s基因多样性指数和Shannon’s信息指数分别为0.2854和0.4390,在居群水平上分别为0.1674和0.2530。NJ聚类分析显示,青岛居群与赣榆居群的亲缘关系最近,而烟台居群与其他4个居群的亲缘关系较远。经Mantel检测,长竹蛏5个居群间的遗传距离与地理距离并无相关性(r=-0.0834,P>0.1)。AMOVA分子变异分析表明,长竹蛏的遗传变异有47.71%发生在居群间,52.29%发生在居群内,居群内的遗传变异大于居群间的遗传变异。长竹蛏5个居群间的遗传分化系数(Gst)为0.2889,基因流(Nm)为1.3194。结果表明,长竹蛏具有较高的遗传多样性,但居群间已发生了一定程度的遗传分化。The razor shell Solen strictus is a member of family Solenidae （Veneroida） bivalve. The Solen strictus dis-tributes widely along the coasts of the Bohai Sea and the Yellow Sea in China, where is a commercial important and potential mariculture species. In this study, genetic diversity in five different geographical populations of the Solen strictus were analyzed by the Inter-Simple Sequence Repeat （ISSR） markers. The samples of the five populations were taken from the off-shores of Dalian （DL）, Yantai （YT）, Laizhou （LZ）, Qingdao （QD） and Ganyu （GY）, respectively. The objectives of present study are： 1） use clear amplified ISSR fragments to examine the genetic variation within and among populations of Solen strictus; 2） lay a foundation of selecting the parent Solen strictus for artificial propagation. Total genomic DNA was extracted from vivisectional foot muscle of two-year-old Solen strictus with standard method. DNA samples were stored at ？20 ℃ until use. The ISSR primers were made by Sangon Inc. （Shanghai, China）, and we used 13 primers which were screened from 30 primers. PCR amplification reaction was carried out in a 25 μL mixture that included 1 × PCR buffer, 2.5 mM of MgCl2, 0.25 mM of dNTP, 0.5μM of primer, 1 unit of Taq DNA po-lymerase, and approximately 40 ng of template DNA. The PCR cycling conditions were： preamplification denaturation at 94 ℃ for 5 min followed by 45 cycles, each cycle included 45s denaturation at 94 ℃ , 45s annealing at 52 ℃, 90s extension at 72 ℃ , and then a final extension at 72 ℃ for 10 min, amplified products resolved by electrophoresis in 1.5% agarose gels. Genetic parameters were calculated by using software POPGENE （version 1.32） that included percentages of po-lymorphic loci, observed number of alleles, effective number of alleles, Nei’s gene diversity, Shannon’s informationindex, genetic differentiation coefficient （Gst）, gene flow （Nm） and Nei’s unbiased genetic distances. The genetic varia-tion

关 键 词：长竹蛏 遗传多样性 ISSR标记 

分 类 号：Q347[生物学—遗传学]