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

被引:23
作者
Baeumler, Stefan
Wulff, Doerte
Tagliani, Laura
Song, Ping
机构
[1] Dow AgroSci LLC, Biotechnol Regulatory Sci, Indianapolis, IN 46268 USA
[2] GeneScan Analyt GmbH, Eurofins, D-79108 Freiburg, Germany
关键词
widestrike cotton; GMO detection; quantitative real-time PCR;
D O I
10.1021/jf0610357
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
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-242365/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 <= 0.04% and <= 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).
引用
收藏
页码:6527 / 6534
页数:8
相关论文
共 17 条
[1]  
Arumuganathan K, 1991, PLANT MOL BIOL REP, V9, P208, DOI [DOI 10.1007/BF02672069, 10.1007/BF02672069]
[2]  
*COD AL COMM, 2005, COD COMM METH AN SAM
[3]  
*EUR COUNC, COMM POS AD COUNC MA
[4]   Development and comparison of four real-time polymerase chain reaction systems for specific detection and quantification of Zea mays L. [J].
Hernández, M ;
Duplan, MN ;
Berthier, G ;
Vaïtilingom, M ;
Hauser, W ;
Freyer, R ;
Pla, M ;
Bertheau, Y .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (15) :4632-4637
[5]  
JAMES C, 2005, 34 ISAAA
[6]   India produces homegrown GM cotton [J].
Jayaraman, K .
NATURE BIOTECHNOLOGY, 2004, 22 (03) :255-256
[7]  
Lipp M, 2005, J AOAC INT, V88, P136
[8]   Detection and traceability of genetically modified organisms in the food production chain [J].
Miraglia, M ;
Berdal, KG ;
Brera, C ;
Corbisier, P ;
Holst-Jensen, A ;
Kok, EJ ;
Marvin, HJP ;
Schimmel, H ;
Rentsch, J ;
van Rie, JPPF ;
Zagon, J .
FOOD AND CHEMICAL TOXICOLOGY, 2004, 42 (07) :1157-1180
[9]   Qualitative and quantitative evaluation of the genomic DNA extracted from GMO and Non-GMO foodstuffs with four different extraction methods [J].
Peano, C ;
Samson, MC ;
Palmieri, L ;
Gulli, M ;
Marmiroli, N .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (23) :6962-6968
[10]  
PRAYL C, 2002, PLANT J, V31, P432