An Hye Suck, Kim Byeong Hak, Lee Jang Wook, Dong Chun Mae, Kim Shin Kwon, Kim Yi Cheong
New Strategy Research Center, National Fisheries Research and Development Institute, Busan 619-705, Korea; E-Mails:
Int J Mol Sci. 2011;12(9):6024-39. doi: 10.3390/ijms12096024. Epub 2011 Sep 16.
Pen shell (Atrina pectinata) is a popular food source with a high commercial value in a number of Asian Pacific areas. The natural A. pectinata population has been declining continuously over the past several decades. Microsatellite DNA markers are a useful DNA-based tool for monitoring the genetic variation of pen shell populations. In this study, 20 polymorphic microsatellite (MS) DNA markers were identified from a partial genomic pen shell DNA library enriched in CA repeats, and used to compare allelic variation between wild and hatchery pen shell populations in Korea. A total of 438 alleles were detected at the 20 MS loci in the two populations. All loci were easily amplified and demonstrated allelic variability, with the number of alleles ranging from 5 to 35 in the wild population and from 5 to 22 in the farmed population. The average observed and expected heterozygosities were 0.69 and 0.82, respectively, in the hatchery samples and 0.69 and 0.83, respectively, in the wild samples. Statistical analysis of fixation index (F(ST)) and analysis of molecular variance (AMOVA) showed minor, but significant, genetic differences between the wild and hatchery populations (F(ST) = 0.0106, CI(95%) = 0.003-0.017). These microsatellite loci may be valuable for future aquaculture and population genetic studies for developing conservation and management plans. Further studies with additional pen shell samples are needed to conclusively determine the genetic diversity between the wild and hatchery populations.
栉江珧(Atrina pectinata)是一种受欢迎的食物来源,在许多亚太地区具有很高的商业价值。在过去几十年中,栉江珧的自然种群数量一直在持续下降。微卫星DNA标记是一种基于DNA的有用工具,可用于监测栉江珧种群的遗传变异。在本研究中,从富含CA重复序列的栉江珧部分基因组DNA文库中鉴定出20个多态性微卫星(MS)DNA标记,并用于比较韩国野生和养殖栉江珧种群之间的等位基因变异。在这两个种群的20个MS位点共检测到438个等位基因。所有位点都易于扩增并表现出等位基因变异性,野生种群中的等位基因数量范围为5至35个,养殖种群中的等位基因数量范围为5至22个。孵化场样本的平均观察杂合度和期望杂合度分别为0.69和0.82,野生样本的平均观察杂合度和期望杂合度分别为0.69和0.83。固定指数(F(ST))的统计分析和分子方差分析(AMOVA)表明,野生和养殖种群之间存在微小但显著的遗传差异(F(ST) = 0.0106,CI(95%) = 0.003 - 0.017)。这些微卫星位点可能对未来的水产养殖和种群遗传学研究有价值,有助于制定保护和管理计划。需要对更多的栉江珧样本进行进一步研究,以最终确定野生和养殖种群之间的遗传多样性。