CAJ | 학술논문

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.
연구이대련、연태、래주、청도화공유근해5개불동지리거군적장죽정(Solen strictus Gould)위실험재료,이용ISSR분자표기진행료유전다양성적연구.결과표명,13개ISSR인물재5개거군중공확증출200개위점,평균매개인물기록15.4개위점,5개거군적다태위점비례위43.56%-60.43%.장죽정재물충수평상적Nei's기인다양성지수화Shannon's신식지수분별위0.2854화0.4390,재거군수평상분별위0.1674화0.2530.NJ취류분석현시,청도거군여공유거군적친연관계최근,이연태거군여기타4개거군적친연관계교원.경Mantel검측,장죽정5개거군간적유전거리여지리거리병무상관성(r=-0.0834,P>0.1).AMOVA분자변이분석표명,장죽정적유전변이유47.71%발생재거군간,52.29%발생재거군내,거군내적유전변이대우거군간적유전변이.장죽정5개거군간적유전분화계수(Gst)위0.2889,기인류(Nm)위1.3194.결과표명,장죽정구유교고적유전다양성,단거군간이발생료일정정도적유전분화.
The razor shell Solen strictus is a member of family Solenidae (Veneroida) bivalve. The Solen strictus distributes 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 ofSolen 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 polymerase, and approximately 40 ng of template DNA. The PCR cycling conditions were: preamplification denaturation at 94℃ for 5 rain 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 polymorphic loci, observed number of alleles, effective number of alleles, Nei's gene diversity, Shannon's information index, genetic differentiation coefficient (Gst), gene flow (Nm) and Nei's unbiased genetic distances. The genetic variation within and among populations of the SoWn strictus was estimated by an analysis of molecular variance (AMOVA) using software WINAMOVA (version 1.55). The dendrogram was constructed on Nei's unbiased genetic distance and neighbor-joining (NJ) cluster analysis which was determined for the five populations and the 100 individuals from these populations by software MEGA (version 4.0), respectively. The Mantel test was taken for correlation between genetic and geographic distance with software TFPGA (version 1.3).The results showed that total of 200 loci from five populations were amplified with 13 primers, average 15.4 loci each primer. The proportion of polymorphie loci in the five populations ranged from 43.56% to 60.43 %. The Nei's gene diversity and Shannon's information index of SoWn strictus was 0.2854 and 0.4390 at species level, 0.1674 and 0.2530 at population level, respectively. NJ cluster analysis indicated that QD population and GY population were the nearest in genetic relationships, and the genetic distance between YT population and other four populations were farther.There was no correlation between genetic and geographic distance among the five populations studied by the Mantel test (r=-0.0834, P>0.1). The AMOVA demonstrated that the among-population component accounted for 47.71% of the total variation, while the within-population component accounted for 52.29%. The within-population genetic variation was apparently larger than the among-population. The genetic differentiation coefficient (Gst) and the gene flow (Nm) were 0.2889 and 1.3194, respectively among the five populations.These data indicates that the genetic diversity of Solen strictus is relatively high, and there is genetic differentiation of some extent among the five populations of Solen strictus. The genetic differentiation among populations could be attributed to the limited remotion and the discontiguous habitat. Anyhow, the results of above research will be helpful for the conservation and utilization of resources, and provide a basis for artificial propagation of Solen strictus.