Literature DB >> 16939306

A real-time quantitative PCR detection method specific to widestrike transgenic cotton (event 281-24-236/3006-210-23).

Stefan Baeumler1, Dörte Wulff, Laura Tagliani, Ping Song.   

Abstract

In compliance with global regulations on transgenic crops, a real-time quantitative PCR method specific to Widestrike transgenic cotton (event 281-24-236/3006-210-23, OECD Unique Identifier DAS-24236-5/DAS-21023-5) was established on the basis of the DNA sequences in the junction between the transgene insert and cotton genome. The optimized method consists of a DNA extraction method for cotton seeds and three PCR systems corresponding to a cotton-specific endogenous reference DNA sequence SAH7 (Sinapis Arabidopsis Homolog 7) and specific detection of event 281-24-236 and event 3006-210-23. The method performance including specificity, sensitivity, accuracy, and precision was determined at a dynamic range of Widestrike DNA levels from 0.04% to 5.0%. The limits of detection (LOD) and quantification (LOQ) were < or =0.04% and < or =0.09%, respectively, at 100 ng of DNA sample per reaction. The quantification results using either the event 281-24-236 or 3006-210-23 system were consistent, and the relative deviation from the expected (true) value was in the range of +/-25%. The robustness of the method was demonstrated by a series of tests with deviations from the optimized assay parameters such as annealing temperature, extension time, PCR instrument, interlaboratory transferability, etc. All the measurements from these tests met the criteria set by EU JRC-CRL (European Commission Joint Research Centre-Community Reference Lab). This real-time quantitative PCR method is accurate and robust, and is recommended as a global benchmark method for the detection and quantification of Widestrike cotton. The method including description, protocol, and performance results is available on the JRC-CRL website (http://gmo-crl.jrc.it/statusofdoss.htm).

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Year:  2006        PMID: 16939306     DOI: 10.1021/jf0610357

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  5 in total

Review 1.  Review of methods for the detection and quantification of adulteration of rice: Basmati as a case study.

Authors:  Lakshminarayana R Vemireddy; V V Satyavathi; E A Siddiq; J Nagaraju
Journal:  J Food Sci Technol       Date:  2014-09-26       Impact factor: 2.701

2.  Digital PCR (dPCR) and qPCR mediated determination of transgene copy number in the forage legume white clover (Trifolium repens).

Authors:  Rafael Narancio; Ulrik John; John Mason; Paula Giraldo; German Spangenberg
Journal:  Mol Biol Rep       Date:  2021-04-16       Impact factor: 2.316

3.  Sensitivity of a real-time PCR method for the detection of transgenes in a mixture of transgenic and non-transgenic seeds of papaya (Carica papaya L.).

Authors:  Madhugiri Nageswara-Rao; Charles Kwit; Sujata Agarwal; Mariah T Patton; Jordan A Skeen; Joshua S Yuan; Richard M Manshardt; C Neal Stewart
Journal:  BMC Biotechnol       Date:  2013-09-01       Impact factor: 2.563

4.  Identification of the Pol Gene as a Species-Specific Diagnostic Marker for Qualitative and Quantitative PCR Detection of Tricholoma matsutake.

Authors:  Luying Shan; Dazhou Wang; Yinjiao Li; Shi Zheng; Wentao Xu; Ying Shang
Journal:  Molecules       Date:  2019-01-28       Impact factor: 4.411

Review 5.  How to deal with the upcoming challenges in GMO detection in food and feed.

Authors:  Sylvia R M Broeders; Sigrid C J De Keersmaecker; Nancy H C Roosens
Journal:  J Biomed Biotechnol       Date:  2012-10-21
  5 in total

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