首页> 外文期刊>中国海洋湖沼学报(英文版) >Isolation and characterization of genic microsatellites from de novo assembly transcriptome in the bivalve Ruditapes philippinarum
【24h】

Isolation and characterization of genic microsatellites from de novo assembly transcriptome in the bivalve Ruditapes philippinarum

机译:菲律宾双壳贝类从头组装转录组中基因微卫星的分离和鉴定

获取原文
获取原文并翻译 | 示例
       

摘要

The marine bivalve Ruditapes philippinarum (Veneridae) has always been an economically important aquaculture species. In this study, 106831 unigenes and 2664 SSR loci (1 locus/40 sequences) were achieved from the de novo assembly transcriptome. Among all the SSRs, tri-nucleotides (46.40%) was the most, followed by di-nucleotides (32.43%). Meanwhile,AAC/GTT (19.82%) was the most common SSR loci searched. After polymorphism detection using 32 wild R. philippinarum individuals, 34 polymorphic and 3 monomorphic SSR loci were screened, and the genetic index of them was calculated. The results show that PIC of 30 polymorphic SSR loci was at medium and high levels (PIC>0.25). However, there were five SSR polymorphic loci (e.g. MG871423, MG871428, MG871429, MG871434, MG871435) deviating from the Hardy-Weinberg equilibrium after the Bonferroni correction (adjusted P=0.001471). The Na value (number of alleles per locus) ranged from 2 to 7. In addition, the Ho (observed heterozygosities) and He (expected heterozygosities) were 0.1000-1.0000 and 0.1913-0.7236, respectively. Therefore, RNA-Seq was shown as a fast and cost-effective method for genic SSR development in non-model species. Meanwhile, the 37 loci from R. philippinarum will further enrich the genetic information and advance the population conservation and restoration.
机译:海洋双壳类菲律宾蛤仔(Rudetapes philippinarum)一直是经济上重要的水产养殖品种。在这项研究中,从头组装转录组获得了106831个单基因和2664个SSR基因座(1个基因座/ 40个序列)。在所有的SSR中,三核苷酸(46.40%)最多,其次是二核苷酸(32.43%)。同时,AAC / GTT(19.82%)是搜索到的最常见的SSR基因座。在利用32个野生菲律宾墨鱼个体进行多态性检测之后,筛选了34个多态性和3个单态SSR基因座,并计算了它们的遗传指数。结果表明,30个多态性SSR基因座的PIC处于中高水平(PIC> 0.25)。但是,在Bonferroni校正后,有五个SSR多态性位点(例如MG871423,MG871428,MG871429,MG871434,MG871435)偏离了Hardy-Weinberg平衡(调整后的P = 0.001471)。 Na值(每个基因座的等位基因数)范围为2至7。此外,Ho(观察到的杂合子)和He(预期杂合子)分别为0.1000-1.0000和0.1913-0.7236。因此,RNA-Seq被证明是一种在非模型物种中进行基因SSR开发的快速且经济高效的方法。同时,来自菲律宾墨鱼的37个基因座将进一步丰富遗传信息,促进种群的保护和恢复。

著录项

  • 来源
    《中国海洋湖沼学报(英文版)》 |2019年第3期|1071-1079|共9页
  • 作者单位

    Fujian Provincial Key Laboratory of Marine Fishery Resources and Eco-Environment, Xiamen 361021, China;

    Fisheries College, Jimei University, Xiamen 361021, China;

    Fujian Provincial Key Laboratory of Marine Fishery Resources and Eco-Environment, Xiamen 361021, China;

    Fisheries College, Jimei University, Xiamen 361021, China;

    Fujian Provincial Key Laboratory of Marine Fishery Resources and Eco-Environment, Xiamen 361021, China;

    Fisheries College, Jimei University, Xiamen 361021, China;

    Fujian Provincial Key Laboratory of Marine Fishery Resources and Eco-Environment, Xiamen 361021, China;

    Fisheries College, Jimei University, Xiamen 361021, China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号