Genetic manipulation of carotenoid biosynthesis in higher plants has been the objective of a number of biotechnology programs,
e.g. the Golden Rice Program. However, tomato (
Solanum
lycopersicum L.), which naturally accumulates lycopene in fruits, has attracted the attention of many groups who have manipulated it to
increase or diversify carotenoid accumulation. One of the most significant achievements was “HighCaro (HC),” a transgenic
tomato plant constitutively expressing the tomato
lycopene beta-cyclase (t
Lcy-b), that produces orange fruits due to the complete conversion of lycopene to
β-carotene. In this article we report the results of a field trial conducted in Metaponto (Italy) on HC and on two control
genotypes to evaluate the stability of the transgenic trait and their yield performances. Transcriptional regulation of eight
genes involved in carotenogenesis was assayed by quantitative real-time PCR (qRT-PCR) analysis on fruits collected at four
distinct development stages. Statistical analysis results demonstrated that in field conditions the transgene maintained its
ability to induce the conversion of lycopene to
β-carotene. Moreover, agronomic performances and fruit quality in the transgenic line were not impaired by this metabolic disturbance.
Results of qRT-PCR analysis suggested that transcription of
PSY-1,
PDS and
ZDS genes were developmentally regulated in both genotypes. Unexpectedly,
Lcy-b expression in transgenic fruits was also developmentally regulated, despite the fact that the gene was driven by a constitutive
promoter. Our data provide evidence that in photosynthetic cells a strict and aspecific mechanism controls the level of transcripts
until the onset of chromoplasts differentiation, at which point a gene-specific control on transcription takes place.
Keywords Genetically modified tomato - Lycopene beta-cyclase - Open-field evaluation - Carotenoids - Quantitative real-time PCR analysis