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用于基因型定量的数字PCR:面食生产链中的一个案例研究。

Digital PCR for Genotype Quantification: A Case Study in a Pasta Production Chain.

作者信息

Morcia Caterina, Terzi Valeria, Ghizzoni Roberta, Vaiuso Chiara, Delogu Chiara, Andreani Lorella, Venturini Andrea, Carnevali Paola, Pompa Pier Paolo, Tumino Giorgio

机构信息

Consiglio per la ricerca in agricoltura e l'analisi dell'economia agraria-Centro di Ricerca Genomica e Bioinformatica (CREA-GB), Via San Protaso 302, 29017 Fiorenzuola d'Arda, Italy.

Consiglio per la ricerca in agricoltura e l'analisi dell'economia agraria-Centro di Ricerca Difesa e Certificazione (CREA-DC), Via Emilia km 307, 26838 Tavazzano, Italy.

出版信息

Biology (Basel). 2021 May 9;10(5):419. doi: 10.3390/biology10050419.

Abstract

Digital polymerase chain reaction (dPCR) is a breakthrough technology based on the partitioning of the analytical sample and detection of individual end-point amplifications into the separate compartments. Among the numerous applications of this technology, its suitability in mutation detection is relevant and characterized by unprecedented levels of precision. The actual applicability of this analytical technique to quantify the presence of a specific plant genotype, in both raw materials and transformed products, by exploiting a point polymorphism has been evaluated. As proof of concept, an Italian premium pasta production chain was considered and a dPCR assay based on a durum wheat target variety private point mutation was designed and evaluated in supply-chain samples. From the results obtained, the assay can be applied to confirm the presence of a target variety and to quantify it in raw materials and transformed products, such as commercial grain lots and pasta. The performance, costs, and applicability of the assay has been compared to analytical alternatives, namely simple sequence repeats (SSRs) and genotype-by-sequencing based on Diversity Arrays Technology sequencing (DArTseq).

摘要

数字聚合酶链反应(dPCR)是一项突破性技术,它基于对分析样品的分区以及对单个终点扩增产物在单独隔室中的检测。在该技术的众多应用中,其在突变检测方面的适用性备受关注,并且具有前所未有的高精度。通过利用单核苷酸多态性,评估了这种分析技术在定量原材料和转化产品中特定植物基因型存在情况方面的实际适用性。作为概念验证,研究考虑了一条意大利优质面食生产链,并设计了一种基于硬粒小麦目标品种私有单核苷酸突变的dPCR检测方法,并在供应链样品中进行了评估。从获得的结果来看,该检测方法可用于确认目标品种的存在,并对原材料和转化产品(如商业粮批和面食)中的目标品种进行定量。已将该检测方法的性能、成本和适用性与分析替代方法进行了比较,即简单序列重复(SSR)和基于多样性阵列技术测序(DArTseq)的基因型测序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bafd/8151192/6325eaf1b4c8/biology-10-00419-g001.jpg

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