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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >The problems and promise of DNA barcodes for species diagnosis of primate biomaterials
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The problems and promise of DNA barcodes for species diagnosis of primate biomaterials

机译:DNA条形码在灵长类生物材料物种诊断中的问题和希望

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摘要

The Integrated Primate Biomaterials and Information Resource (www.IPBIR.org) provides essential research reagents to the scientific community by establishing, verifying, maintaining, and distributing DNA and RNA derived from primate cell cultures. The IPBIR uses mitochondrial cytochrome c oxidase subunit I sequences to verify the identity of samples for quality control purposes in the accession, cell culture, DNA extraction processes and prior to shipping to end users. As a result, IPBIR is accumulating a database of 'DNA barcodes' for many species of primates. However, this quality control process is complicated by taxon specific patterns of 'universal primer' failure, as well as the amplification or co-amplification of nuclear pseudogenes of mitochondrial origins. To overcome these difficulties, taxon specific primers have been developed, and reverse transcriptase PCR is utilized to exclude these extraneous sequences from amplification. DNA barcoding of primates has applications to conservation and law enforcement. Depositing barcode sequences in a public database, along with primer sequences, trace files and associated quality scores, makes this species identification technique widely accessible. Reference DNA barcode sequences should be derived from, and linked to, specimens of known provenance in web-accessible collections in order to validate this system of molecular diagnostics.
机译:灵长类动物生物材料和信息资源综合资源(www.IPBIR.org)通过建立,验证,维护和分配源自灵长类动物细胞培养物的DNA和RNA,为科学界提供了重要的研究试剂。 IPBIR使用线粒体细胞色素C氧化酶亚基I序列来验证样品的身份,以便在入库,细胞培养,DNA提取过程中以及运输给最终用户之前进行质量控制。结果,IPBIR正在积累许多灵长类动物的“ DNA条码”数据库。但是,这种质量控制过程由于“通用引物”失效的分类单元特定模式以及线粒体起源的核假基因的扩增或共扩增而变得复杂。为了克服这些困难,已经开发了分类群特异性引物,并且利用逆转录酶PCR从扩增中排除了这些无关序列。灵长类动物的DNA条形码可应用于保护和执法。将条形码序列以及引物序列,跟踪文件和相关的质量得分存储在公共数据库中,使得该物种识别技术可广泛使用。参考DNA条码序列应源自可访问网络的馆藏中已知来源的标本,并与之链接,以验证该分子诊断系统。

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