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Living Modified Organism (LMO)
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Purple Tomato
EN
Del/Ros1
No
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Organization:Norfolk Plant Sciences (NPS)Private sector (business and industry)Norfolk Plant Sciences Ltd, John Innes Centre, Colney LaneNorwich, Norfolk
NR4 7UH, United Kingdom of Great Britain and Northern IrelandPhone: +44 (0)1603 255839,Fax:Email: info@norfolkplantsciences.com,Website: http://www.norfolkplantsciences.com/,
The tomato (Solanum lycopersicum) was engineered to have a purple coloration and contain increased levels of antioxidants. To achieve this, the tomato expresses the Antirrhinum majus transcription factors ROSEA1 and DELILA, which interact to upregulate the the genes associated with anthocyanin biosynthesis in the tomato. As such, the levels of tomato anthocyanins delphinidin 3-O-(coumaroyl) rutinoside-5-O-glucoside and petunidin 3-O-(coumaroyl) rutinoside-5-O-glucoside are elevated in the flesh of the modified tomato fruit, resulting in a deep purple colour. In addition to the transcription factors, the modified tomato also contains an Escherichia coli neomycin phosphotransferase II gene cassette, which was used for neomycin selection during transformation.
The term “Recipient organism” refers to an organism (either already modified or non-modified) that was subjected to genetic modification, whereas “Parental organisms” refers to those that were involved in cross breeding or cell fusion.
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BCH-ORGA-SCBD-12079-5 Organism Solanum lycopersicum (Tomato, SOLLC)Crops
MicroTom variety
EN
pDEL.ROS
EN
- Agrobacterium-mediated DNA transfer
0.708 kb
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0.795 kb
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0.180 kb
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Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
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BCH-GENE-SCBD-100290-6 CaMV 35S terminator | Cauliflower mosaic virus (CaMV)Terminator
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BCH-GENE-SCBD-263014-1 Rosea1 | Antirrhinum majus (Common Snapdragon, Snapdragon)Protein coding sequence | Changes in quality and/or metabolite content (Antioxidants, Pigmentation / Coloration)
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BCH-GENE-SCBD-104862-2 E8 gene promoter | Solanum lycopersicum (Tomato, SOLLC)Promoter
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BCH-GENE-SCBD-263013-2 Delila | Antirrhinum majus (Common Snapdragon, Snapdragon)Protein coding sequence | Changes in quality and/or metabolite content (Antioxidants, Pigmentation / Coloration)
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BCH-GENE-SCBD-100271-5 Octopine Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminator
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BCH-GENE-SCBD-15001-5 Neomycin Phosphotransferase II | Escherichia coli (ECOLX)Protein coding sequence | Resistance to antibiotics (Kanamycin)
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BCH-GENE-SCBD-100270-6 Nopaline Synthase Gene Promoter | Agrobacterium tumefaciens (Agrobacterium)Promoter
The modified tomato contains three gene cassettes: Antirrhinum majus rosea1 (ros1), A. majus delila (del) and Escherichia coli neomycin phosphotransferase II (nptII).
The ros1 coding sequence is under control of a tomato E8 promoter and Cauliflower mosaic virus (CaMV) 35S terminator. The E8 promoter is a fruit specific promoter and thus expression of ROS1 will be restricted to the fruit.
The del coding sequence is under control of a tomato E8 promoter and CaMV 35S terminator. The E8 promoter is a fruit specific promoter and thus expression of DEL will be restricted to the fruit.
The nptII coding sequence is under control of an Agrobacterium tumefaciens nopaline synthase promoter and octopine synthase terminator.
Note:
The ros1 coding sequence is under control of a tomato E8 promoter and Cauliflower mosaic virus (CaMV) 35S terminator. The E8 promoter is a fruit specific promoter and thus expression of ROS1 will be restricted to the fruit.
The del coding sequence is under control of a tomato E8 promoter and CaMV 35S terminator. The E8 promoter is a fruit specific promoter and thus expression of DEL will be restricted to the fruit.
The nptII coding sequence is under control of an Agrobacterium tumefaciens nopaline synthase promoter and octopine synthase terminator.
Note:
- Sequencing analysis indicated that the T-DNA was inserted into Chromosome 4 of the tomato genome (between basepair position 62904677 and 62904771). The insertion of the T-DNA resulted in a 94 basepair deletion of the tomato genome.
- Sequencing analysis also indicated that no vector backbone sequences were integrated into the tomato genome.
- Northern blot analysis indicated that the following enzymes were upregulated: phenylalanine ammonia lyase; 4-coumarate 3-hydroxylase; flavanone-3-hydroxylase; flavonoid-3'5'-hydroxylase; anthocyanidin synthase; flavonoid 3-O-glucosyltransferase; anthocyanin acyltransferase; flavonoid-5-glucosyltransferase; glutathione S-transferase and putative anthocyanin transporter
EN
- Food
EN
EN
- APHIS - Information supporting a regulatory status review of tomato genetically engineered to produce increased level of anthocyanins [PDF - 5.82 MB] [ English ]
- Norfolk Plant Sciences - Big Purple Tomato [ English ]
- NCBI GenBank - Plant binary expression vector pDEL.ROS, complete sequence [ English ]
- European Nucleotide Archive - Illumina HiSeq X Ten paired end sequencing - Purple tomato [ English ]
- Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors.pdf [ English ]
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