International Collaborative Study of the Endogenous Reference Gene, Sucrose Phosphate Synthase (SPS), Used for Qualitative and Quantitative Analysis of Genetically Modified Rice

被引:42
作者
Jiang, Lingxi [1 ]
Yang, Litao [1 ]
Zhang, Haibo [1 ]
Guo, Jinchao [1 ]
Mazzara, Marco [2 ]
Van den Eede, Guy [2 ]
Zhang, Dabing [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Bor Luh Food Safety Ctr, GMO Detect Lab, Shanghai 200240, Peoples R China
[2] European Commiss, Joint Res Ctr, Inst Hlth & Consumer Protect, Biotechnol & GMOs Unit, I-21027 Ispra, Italy
关键词
Collaborative trial; sucrose phosphate synthase; endogenous reference gene; Oryza sativa; qualitative and quantitative PCR; POLYMERASE-CHAIN-REACTION; REAL-TIME; PCR DETECTION; MODIFIED ORGANISMS; TRANSGENIC RAPESEED; REACTION SYSTEMS; DNA EXTRACTS; 35S PROMOTER; ZEA-MAYS; QUANTIFICATION;
D O I
10.1021/jf803166p
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
One rice (Oryza sativa) gene, sucrose phosphate synthase (SPS), has been proven to be a suitable endogenous reference gene for genetically modified (GM) rice detection in a previous study. Herein are the reported results of an international collaborative ring trial for validation of the SPS gene as an endogenous reference gene and its optimized qualitative and quantitative polymerase chain reaction (PCR) systems. A total of 12 genetically modified organism (GMO) detection laboratories from seven countries participated in the ring trial and returned their results. The validated results confirmed the species specificity of the method through testing 10 plant genomic DNAs, low heterogeneity, and a stable single-copy number of the rice SPS gene among 7 indica varieties and 5 japonica varieties. The SPS qualitative PCR assay was validated with a limit of detection (LOD) of 0.1%, which corresponded to about 230 copies of haploid rice genomic DNA, while the limit of quantification (LOQ) for the quantitative PCR system was about 23 copies of haploid rice genomic DNA, with acceptable PCR efficiency and linearity. Furthermore, the bias between the test and true values of eight blind samples ranged from 5.22 to 26.53%. Thus, we believe that the SPS gene is suitable for use as an endogenous reference gene for the identification and quantification of GM rice and its derivates.
引用
收藏
页码:3525 / 3532
页数:8
相关论文
共 34 条
[1]  
[Anonymous], 2003, Official Journal of the European Union, VL268, P1
[2]   A real-time quantitative PCR detection method specific to widestrike transgenic cotton (event 281-24-236/3006-210-23) [J].
Baeumler, Stefan ;
Wulff, Doerte ;
Tagliani, Laura ;
Song, Ping .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (18) :6527-6534
[3]   A strategy for designing multi-taxa specific reference gene systems.: Example of application -: ppi phosphofructokinase (ppi-PPF) used for the detection and quantification of three taxa:: Maize (Zea mays), cotton (Gossypium hirsutum) and rice (Oryza sativa) [J].
Chaouachi, Maher ;
Giancola, Sandra ;
Romaniuk, Marcel ;
Laval, Valerie ;
Bertheau, Yves ;
Brunel, Dominique .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (20) :8003-8010
[4]   Validation of a rice specific gene, sucrose phosphate synthase, used as the endogenous reference gene for qualitative and real-time quantitative PCR detection of transgenes [J].
Ding, JY ;
Jia, JW ;
Yang, LT ;
Wen, HB ;
Zhang, CM ;
Liu, WX ;
Zhang, DB .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (11) :3372-3377
[5]  
Feinberg M, 2005, J AOAC INT, V88, P558
[6]  
Fernandez S, 2005, J AOAC INT, V88, P547
[7]   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
[8]   Real-time polymerase chain reaction based assays for quantitative detection of barley, rice, sunflower, and wheat [J].
Hernández, M ;
Esteve, T ;
Pla, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (18) :7003-7009
[9]   Real-time and conventional polymerase chain reaction systems based on the metallo-carboxypeptidase inhibitor gene for specific detection and quantification of potato and tomato in processed food [J].
Hernández, M ;
Ferrando, A ;
Esteve, T ;
Puigdoménech, P ;
Prat, S ;
Pla, M .
JOURNAL OF FOOD PROTECTION, 2003, 66 (06) :1063-1070
[10]   A rapeseed-specific gene, Acetyl-CoA carboxylase, can be used as a reference for qualitative and real-time quantitative PCR detection of transgenes from mixed food samples [J].
Hernández, M ;
Río, A ;
Esteve, T ;
Prat, S ;
Pla, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (08) :3622-3627