Screening and construct-specific detection methods of transgenic Huafan No 1 tomato by conventional and real-time PCR
文献类型: 外文期刊
第一作者: Yang, LT
作者: Yang, LT;Shen, HF;Pan, AH;Chen, JX;Huang, C;Zhang, DB
作者机构:
关键词: Huafan No 1 tomato;conventional and real-time PCR;genetically modified organisms;screening and construct-specific detection
期刊名称:JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE ( 影响因子:3.638; 五年影响因子:3.802 )
ISSN: 0022-5142
年卷期: 2005 年 85 卷 13 期
页码:
收录情况: SCI
摘要: Genetically modified (GM) tomatoes have been approved for commercialization in many countries since the first GM tomato FLAVR SAVR was permitted for planting in 1994. In China, GM tomato Huafan No I with a character of long shelf-life was the first GM plant which was approved for commercialization in 1996. To meet the requirement of the GM tomatoes labeling policy that has been actualized in China since 2001, screening and construct-specific PCR detection methods for detecting the universal elements transformed into tomato, such as cauliflower mosaic virus 35S (CaMV35s) promoter and the nopaline synthase (NOS) terminator of Agrobacterium tumefaciens, and the specifically inserted heterologous DNA sequence between CaMV35s promoter and anti-sense ethylene-forming enzyme (EFE) gene were set up. To make the detection methods normative, a novel single copy tomato gene LAT52 was also used as an endogenous reference gene in the PCR detection systems. The limit of detection of screening and construct specific detection methods for Huafan No 1 was 68 haploid genome copies in conventional PCR detection, and three copies in TaqMan real-time PCR detection. The limit of quantitation of screening quantitative PCR assays for Huafan No 1 was three copies and was 25 copies for construct-specific quantitative PCR. Two samples with known Huafan No I tomato content were detected using the established conventional and real-time PCR systems, and these results also indicated that the established Huafan No I screening and construct-specific PCR detection systems were reliable, sensitive and accurate. (c) 2005 Society of Chemical Industry.
分类号:
- 相关文献
作者其他论文 更多>>
-
Oral immunization of mice with plant-derived fimbrial adhesin FaeG induces systemic and mucosal K88ad enterotoxigenic Escherichia coli-specific immune responses
作者:Liang, WQ;Huang, YH;Yang, XH;Zhou, Z;Pan, AH;Qian, BJ;Huang, C;Chen, JX;Zhang, DB
关键词:enterotoxigenic Escherichia coli;proteinaceous fimbriae;recombinant FaeG;transgenic tobacco
-
Duplication and expression analysis of multicopy miRNA gene family members in Arabidopsis and rice
作者:Jiang, DH;Yin, CS;Yu, AP;Zhou, XF;Liang, WQ;Yuan, Z;Xu, Y;Yu, QB;Wen, TQ;Zhang, DB
关键词:gene duplication;microRNA;multicopy
-
Event-specific qualitative and quantitative PCR detection of MON863 maize based upon the 3 '-transgene integration sequence
作者:Yang, LT;Xu, SC;Yin, CS;Zhang, KW;Wang, ZY;Zhang, DB
关键词:qualitative and quantitative PCR;GMOs;event-specific detection;MON863;TAIL-PCR;transgene integration
-
Identification of products formed in side reactions in ractopamine synthesis with electrospray ionization-mass spectrometry
作者:Chen, JX;Chen, ZL;Ma, AD;Chen, WM;Yang, ZL
关键词:electrospray ionization-mass spectrometry;collisional activation;ractopamine synthesis;side reaction products
-
Validation of a cotton-specific gene, Sad1, used as an endogenous reference gene in qualitative and real-time quantitative PCR detection of transgenic cottons
作者:Yang, LT;Chen, JX;Huang, C;Liu, YH;Jia, SR;Pan, LW;Zhang, DB
关键词:Gossypium hirsutum;stearoyl-acyl carrier protein desaturase gene;endogenous reference gene;genetically modified organism;conventional and real-time PCR
-
Estimating the copy number of transgenes in transformed rice by real-time quantitative PCR
作者:Yang, LT;Ding, JY;Zhang, CM;Jia, JW;Weng, HB;Liu, WX;Zhang, DB
关键词:transgenic rice;TaqMan real-time PCR;GUS;HPT;copy number
-
Genetic analysis and mapping of rice (Oryza sativa L.) male-sterile (OsMS-L) mutant
作者:Liu, HS;Chu, HW;Li, H;Wang, HM;Wei, JL;Li, N;Ding, SY;Huang, H;Ma, H;Huang, CF;Luo, D;Yuang, Z;Liu, JH;Zhang, DB
关键词:rice (Oryza sativa L.);mutants;male-sterility;gene mapping;molecular marker