Whole genome sequence analysis of unidentified genetically modified papaya for development of a specific detection method

被引:5
作者
Nakamura, Kosuke [1 ]
Kondo, Kazunari [1 ]
Akiyama, Hiroshi [1 ]
Ishigaki, Takumi [1 ]
Noguchi, Akio [1 ]
Katsumata, Hiroshi [2 ]
Takasaki, Kazuto [2 ]
Futo, Satoshi [2 ]
Sakata, Kozue [1 ]
Fukuda, Nozomi [1 ]
Mano, Junichi [3 ]
Kitta, Kazumi [3 ]
Tanaka, Hidenori [4 ]
Akashi, Ryo [4 ]
Nishimaki-Mogami, Tomoko [1 ]
机构
[1] Natl Inst Hlth Sci, Setagaya Ku, 1-18-1 Kamiyoga, Tokyo 1588501, Japan
[2] FASMAC CO LTD, 5-1-3 Midorigaoka, Atsugi, Kanagawa 2430041, Japan
[3] Natl Agr & Food Res Org, Natl Food Res Inst, Analyt Sci Div, 2-1-12 Kannondai, Tsukuba, Ibaraki 3058642, Japan
[4] Miyazaki Univ, Grad Sch Agr, 1-1 Gakuen Kibanadai Nishi, Miyazaki 8892192, Japan
关键词
Genetically modified; Transgenic sequence; Next-generation sequencer; Genome sequence; Real-time PCR; Carica papaya L; PCR DETECTION METHODS; RINGSPOT VIRUS; MODIFIED ORGANISMS; SCREENING METHOD; RECOMBINANT-DNA; FOOD-PRODUCTS; T-DNA; RESISTANT; IDENTIFICATION; STRAINS;
D O I
10.1016/j.foodchem.2016.02.157
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Identification of transgenic sequences in an unknown genetically modified (GM) papaya (Carica papaya L.) by whole genome sequence analysis was demonstrated. Whole genome sequence data were generated for a GM-positive fresh papaya fruit commodity detected in monitoring using real-time polymerase chain reaction (PCR). The sequences obtained were mapped against an open database for papaya genome sequence. Transgenic construct-and event-specific sequences were identified as a GM papaya developed to resist infection from a Papaya ringspot virus. Based on the transgenic sequences, a specific real-time PCR detection method for GM papaya applicable to various food commodities was developed. Whole genome sequence analysis enabled identifying unknown transgenic construct-and event-specific sequences in GM papaya and development of a reliable method for detecting them in papaya food commodities. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:272 / 279
页数:8
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