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利用 454 高通量测序评估超大型磷虾线粒体基因组的群体水平变异。

Assessing population-level variation in the mitochondrial genome of Euphausia superba using 454 next-generation sequencing.

机构信息

Cooperative Institute for Marine Resources Studies, Hatfield Marine Science Center, Oregon State University, Newport, OR, USA.

出版信息

Mol Biol Rep. 2012 May;39(5):5755-60. doi: 10.1007/s11033-011-1385-y. Epub 2012 Jan 5.

Abstract

The Antarctic krill (Euphausia superba Dana 1852) is widely distributed throughout the Southern Ocean, where it provides a key link between primary producers and upper trophic levels and supports a major commercial fishery. Despite its ecological and commercial importance, genetic population structure of the Antarctic krill remains poorly described. In an attempt to illuminate genetic markers for future population and phylogenetic analysis, five E. superba mitogenomes, from samples collected west of the Antarctic Peninsula, were sequenced using new 454 next-generation sequencing techniques. The sequences, of lengths between 13,310 and 13,326 base pairs, were then analyzed in the context of two previously-published near-complete sequences. Sequences revealed relatively well-conserved partial mitochondrial genomes which included complete sequences for 11 of 13 protein-coding genes, 16 of 23 tRNAs, and the large ribosomal subunit. Partial sequences were also recovered for cox1 and the small ribosomal subunit. Sequence analysis suggested that the cox2, nad5, and nad6 genes would be the best candidates for future population genetics analyses, due to their high number of variable sites. Future work to reveal the noncoding control region remains.

摘要

南极磷虾(Euphausia superba Dana 1852)广泛分布于南大洋,在那里它将初级生产者和上层营养级联系起来,并支持着一个主要的商业渔业。尽管南极磷虾具有生态和商业上的重要性,但它的遗传种群结构仍然描述得很差。为了阐明未来种群和系统发育分析的遗传标记,我们使用新的 454 新一代测序技术,对来自南极半岛西部的样本中的 5 个南极磷虾线粒体基因组进行了测序。这些序列长度在 13310 到 13326 个碱基对之间,然后在两个先前发表的近完整序列的背景下进行了分析。序列显示了相对保守的部分线粒体基因组,其中包括 13 个蛋白质编码基因中的 11 个、23 个 tRNA 中的 16 个以及大亚基核糖体的完整序列。cox1 和小亚基核糖体的部分序列也被回收。序列分析表明,cox2、nad5 和 nad6 基因由于其可变位点数量多,将是未来种群遗传学分析的最佳候选基因。未来的工作仍然需要揭示非编码控制区。

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