首页> 外文期刊>Biochemical Systematics and Ecology >Haplotype-specific single-locus multiplex PCR assay for molecular identification of sea-bob shrimp, Xiphopenaeus kroyeri (Heller, 1862), cryptic species from the Southwest Atlantic using a DNA pooling strategy for simultaneous identification of multiple samples
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Haplotype-specific single-locus multiplex PCR assay for molecular identification of sea-bob shrimp, Xiphopenaeus kroyeri (Heller, 1862), cryptic species from the Southwest Atlantic using a DNA pooling strategy for simultaneous identification of multiple samples

机译:单倍型特异性单位点多重PCR分析,用于鉴定来自西南大西洋的海隐虾Xiphopenaeus kroyeri(Heller,1862)的隐性物种,使用DNA池策略同时鉴定多个样品

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摘要

This work describes a single-locus multiplex PCR assay based on partial COI mitochondrial gene polymorphisms for identification of two Atlantic cryptic species of the sea-bob shrimp, Xiphopenaeus kroyeri (Heller, 1862) that were recently identified using molecular approaches. Reliable identification of cryptic species of Xiphopenaeus spp. has fundamental implications for management and conservation of the sea-bob shrimp fishery stocks. The assay was developed based on sequence polymorphisms of 130 specimens of both species, comprising samples from Venezuela to the southern coast of Brazil, validated by the amplification of 368 adult shrimp samples from nine different locations and confirmed by direct sequencing. The methodology has been optimized to enable the identification of equi-molar mixtures of DNA from up to 10 individuals by PCR reaction, allowing the fast and cheap identification of many specimens for large scale studies on fisheries biology and population genetics. The DNA pooling strategy enabled the identification of a new locality of occurrence of Xiphopenaeus sp. II in the Brazilian coast, Caravelas, indicating that the species distribution may be continuous on the coast, and not disjoint as observed so far
机译:这项工作描述了一种基于部分COI线粒体基因多态性的单基因座多重PCR检测方法,用于鉴定两种最近发现使用分子方法鉴定的海对虾的大西洋隐性物种Xiphopenaeus kroyeri(Heller,1862)。可靠的剑灵隐孢子虫种的鉴定。对海虾虾类渔业资源的管理和保护具有根本意义。该测定法是基于130个两个物种的样本的序列多态性而开发的,包括从委内瑞拉到巴西南部海岸的样本,并通过从9个不同位置扩增368个成年虾样本进行了验证,并通过直接测序进行了确认。该方法已经过优化,可以通过PCR反应从多达10个个体中鉴定出等摩尔的DNA混合物,从而可以快速,廉价地鉴定许多标本,以进行大规模的渔业生物学和种群遗传学研究。 DNA合并策略使得能够鉴定新出现的剑灵藻。巴西卡拉维拉斯海岸的II号,表明该物种在海岸上的分布可能是连续的,并且到目前为止还没有分离

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