Evaluation of the reliability of maize reference assays for GMO quantification

被引:17
作者
Papazova, Nina [1 ]
Zhang, David [2 ]
Gruden, Kristina [3 ]
Vojvoda, Jana [3 ]
Yang, Litao [4 ]
Gasparic, Meti Buh [3 ]
Blejec, Andrej [3 ]
Fouilloux, Stephane [2 ]
De Loose, Marc [1 ]
Taverniers, Isabel [1 ]
机构
[1] Inst Agr & Fisheries Res ILVO, B-9820 Merelbeke, Belgium
[2] Lab BioGEVES, GEVES Domaine Magneraud, F-17700 Surgeres, France
[3] Natl Inst Biol, Dept Biotechnol & Syst Biol, Ljubljana 1000, Slovenia
[4] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, GMO Detect Lab, SJTU Bor Luh Food Safety Ctr, Shanghai 200240, Peoples R China
关键词
GMO; Real-time PCR quantification; Endogenous target taxon; Reference assay; Reliability; GENETICALLY-MODIFIED MAIZE; ZEA-MAYS; DNA; QUANTITATION; DIVERSITY; GENE; SYSTEMS; REGIONS;
D O I
10.1007/s00216-009-3386-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A reliable PCR reference assay for relative genetically modified organism (GMO) quantification must be specific for the target taxon and amplify uniformly along the commercialised varieties within the considered taxon. Different reference assays for maize (Zea mays L.) are used in official methods for GMO quantification. In this study, we evaluated the reliability of eight existing maize reference assays, four of which are used in combination with an event-specific polymerase chain reaction (PCR) assay validated and published by the Community Reference Laboratory (CRL). We analysed the nucleotide sequence variation in the target genomic regions in a broad range of transgenic and conventional varieties and lines: MON 810 varieties cultivated in Spain and conventional varieties from various geographical origins and breeding history. In addition, the reliability of the assays was evaluated based on their PCR amplification performance. A single base pair substitution, corresponding to a single nucleotide polymorphism (SNP) reported in an earlier study, was observed in the forward primer of one of the studied alcohol dehydrogenase 1 (Adh1) (70) assays in a large number of varieties. The SNP presence is consistent with a poor PCR performance observed for this assay along the tested varieties. The obtained data show that the Adh1 (70) assay used in the official CRL NK603 assay is unreliable. Based on our results from both the nucleotide stability study and the PCR performance test, we can conclude that the Adh1 (136) reference assay (T25 and Bt11 assays) as well as the tested high mobility group protein gene assay, which also form parts of CRL methods for quantification, are highly reliable. Despite the observed uniformity in the nucleotide sequence of the invertase gene assay, the PCR performance test reveals that this target sequence might occur in more than one copy. Finally, although currently not forming a part of official quantification methods, zein and SSIIb assays are found to be highly reliable in terms of nucleotide stability and PCR performance and are proposed as good alternative targets for a reference assay for maize.
引用
收藏
页码:2189 / 2201
页数:13
相关论文
共 30 条
  • [1] [Anonymous], 2003, Stigmatisation et discrimination, P1
  • [2] Arumuganathan K., 1991, PLANT MOL BIOL REP, V9, P229, DOI [DOI 10.1007/BF02672073, 10.1007/BF02672073]
  • [3] Insertion-deletion polymorphisms in 3′ regions of maize genes occur frequently and can be used as highly informative genetic markers
    Bhattramakki, D
    Dolan, M
    Hanafey, M
    Wineland, R
    Vaske, D
    Register, JC
    Tingey, SV
    Rafalski, A
    [J]. PLANT MOLECULAR BIOLOGY, 2002, 48 (05) : 539 - 547
  • [4] A single nucleotide polymorphism (SNP839) in the adh1 reference gene affects the quantitation of genetically modified maize (Zea mays L.)
    Broothaerts, Wim
    Corbisier, Philippe
    Schimmel, Heinz
    Trapmann, Stefanie
    Vincent, Sandra
    Emons, Hendrik
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (19) : 8825 - 8831
  • [5] Quantification of the detrimental effect of a single primer-template mismatch by real-time PCR using the 16S rRNA gene as an example
    Bru, D.
    Martin-Laurent, F.
    Philippot, L.
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (05) : 1660 - 1663
  • [6] Evolution of DNA sequence nonhomologies among maize inbreds
    Brunner, S
    Fengler, K
    Morgante, M
    Tingey, S
    Rafalski, A
    [J]. PLANT CELL, 2005, 17 (02) : 343 - 360
  • [7] CEDDIA M, 2008, 23443 EUR EN
  • [8] 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)
    Chaouachi, Maher
    Giancola, Sandra
    Romaniuk, Marcel
    Laval, Valerie
    Bertheau, Yves
    Brunel, Dominique
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (20) : 8003 - 8010
  • [9] Emrich SJ, 2007, GENETICS, V175, P429, DOI 10.1534/genetics.106.064006
  • [10] Assessment of Primer/Template Mismatch Effects on Real-Time PCR Amplification of Target Taxa for GMO Quantification
    Ghedira, Rim
    Papazova, Nina
    Vuylsteke, Marnik
    Ruttink, Tom
    Taverniers, Isabel
    De Loose, Marc
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2009, 57 (20) : 9370 - 9377