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Application of the first internal transcribed spacer (ITS-1) of ribosomal DNA as a molecular marker to population analysis in farrer's scallop Chlamys farreri

机译:核糖体DNA的第一个内部转录间隔子(ITS-1)作为分子标记在法拉扇贝(Chlamys farreri)种群分析中的应用

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Sequence variation of the first internal transcribed spacer of ribosomal DNA (ITS-1) was examined and its application to the study of genetic variation was explored in four populations of farrer's scallop Chlamys farreri. ITS-1 fragments,with a length of about 300 bp,of 78 individuals collected from Dalian, Qingdao, Yantai in China and Korea respectively were amplified via PCR, cloned and sequenced. Intra-genomic variation was examined by sequencing several clones of single individuals. Alignment and polymorphism analysis detected 44 haplotypes and 50 polymorphic sites which consist of 30 substitutions and 20 indels, indicating a high level of polymorphisms. Sequence analysis also showed a very low level of intra-individual variation. All these features validated the feasibility of application of ITS-1 fragment to population analysis. Polymorphism analysis showed that the Korea sample has the richest genetic variation, followed by Yantai and Qingdao samples. AMOVA (analysis of molecular variance) showed that the majority (96.26%) of genetic variation was distributed within populations and 3.74% resulted from among populations, but with P<0.05 (= 0.042), indicating that the populations in this study have significant divergence. This output was basically concordant with the result arising from RAPD data and different from that from mitochondrial 16S rDNA sequence data. Discussion on this inconsistency was made accordingly.
机译:研究了核糖体DNA的第一个内部转录间隔区(ITS-1)的序列变异,并探讨了其在四个法拉扇贝扇贝(Chlamys farreri)种群中的遗传变异研究应用。分别从中国大连,青岛,烟台和韩国采集的78例个体中的ITS-1片段长约300 bp,通过PCR扩增,克隆和测序。通过测序单个个体的几个克隆检查基因组内变异。比对和多态性分析检测到44个单倍型和50个多态性位点,由30个取代和20个插入/缺失组成,表明高水平的多态性。序列分析还显示出非常低的个体内变异水平。所有这些特征证实了将ITS-1片段应用于人群分析的可行性。多态性分析表明,韩国样本的遗传变异最丰富,其次是烟台和青岛样本。 AMOVA(分子变异分析)表明,遗传变异的大部分(96.26%)分布于种群内,而种群间遗传变异占3.74%,但P <0.05(= 0.042),表明该研究人群具有显着差异。 。此输出基本上与RAPD数据产生的结果一致,并且与线粒体16S rDNA序列数据的结果不同。对此进行了讨论。

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