Plant haemoglobin genes are known to occur in legume and non-legume families and in both nodulating (e.g., Parasponia andersonii) and non-nodulating species (e.g., Trema tomentosa). Their presence in non-nondulating plants raises the possibility that haemoglobins might serve a function in non-symbio
Sucrose-regulated expression of a chimeric potato tuber gene in leaves of transgenic tobacco plants
β Scribed by Herman Wenzler; Gregory Mignery; Linda Fisher; William Park
- Publisher
- Springer
- Year
- 1989
- Tongue
- English
- Weight
- 665 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0167-4412
No coin nor oath required. For personal study only.
β¦ Synopsis
Patatin is a family of lipid acyl hydrolases that accounts for 30 to 40 ~o of the total soluble protein in potato tubers. Class-I patatin genes encode 98 to 99~ of the patatin mRNA in tubers, but are not normally expressed in other tissues. They are not totally 'tuber-specific'; however, since they can be induced to express at high levels in other tissues under conditions of sink limitation or in explants cultured on medium containing elevated levels of sucrose. To examine the evolution of the mechanisms that regulate patatin gene expression, we introduced a chimeric patatin-fl-glucuronidase (GUS) gene containing 2.5 kb of 5' flanking sequence from the Class-I potato patatin gene PS20 into tobacco plants. The construct was not expressed at significant levels in leaves of juvenile plants or plantlets cultured in vitro, but was expressed at high levels in explants cultured on medium containing 0.3 to 0.4 M sucrose. While there were differences in the expression of the chimeric gene between transgenic tobacco and potato plants, the pattern of sucrose induction was very similar. These results suggest that the mechanism that controls patatin gene expression in potato tubers evolved from a widely distributed mechanism in which gene expression is regulated by the level of available photosynthate.
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## Summary This report describes the analysis of transgenic potato plants stably transformed with chimeric genes comprising either a patatin (tuberβspecific) or a STβLS1 (leafβ and stemβspecific) gene promoter and a potato sucrose nonβfermentingβ1 (SNF1)βrelated protein kinase gene (PKIN1) sequence
The gene for human epidermal growth factor (hEGF) was chemically synthesized and used for expression in transgenic potato. The hEGF coding sequence was modified by PCR to introduce ATG start codon and fused either to the 35S cauliflower mosaic virus promoter or to the patatin class I promoter. The h