Abstract
The pattern and expression level of β-glucuronidase (gus) reporter gene regulated by six heterologous promoters were studied in transgenic Populus tremula × P. alba plants obtained by Agrobacterium-mediated transformation. Binary vector constructs used contained the following promoter sequences: the CaMV35S from cauliflower mosaic virus; its duplicated version fused to the enhancer sequence from alfalfa mosaic virus; CsVMV from cassava vein mosaic virus; ubiquitin 3 from Arabidopsis thaliana (UBQ3); S-adenosyl-L-methionine synthetase (Sam-s) from soybean; and the rolA from Agrobacterium rhizogenes. Histochemical staining of root, stem and leaf tissues showed phloem and xylem-specific gus expression under rolA promoter, and constitutive expression with the other putative constitutive promoters. Quantitative GUS expression of 10 – 15 independently transformed in vitro grown plants, containing each promoter, was determined by fluorimetric GUS assays. The UBQ3-gus fusion induced the highest average expression level, although an extensive variation in expression levels was observed between independent transgenic lines for all the constructs tested.
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Abbreviations
- 35S-D:
-
duplicated version of CaMV35S promoter fused to the enhancer sequence from alfalfa mosaic virus
- CaMV35S:
-
35S promoter from cauliflower mosaic virus
- CsVMV:
-
promoter from cassava vein mosaic virus
- EDTA:
-
ethylene diamine tetraacetic acid
- GUS:
-
β-glucuronidase
- MU:
-
4-methylumbelliferone
- MUG:
-
4-methylumbelliferyl-β-D-glucuronide
- rolA:
-
promoter from rolA gene from Agrobacterium rhizogenes
- Sam-s:
-
promoter from S-adenosyl-L-methionine synthetase gene from Glycine max
- UBQ3:
-
promoter from ubiquitin 3 gene from Arabidopsis thaliana
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Studart-Guimaraes, C., Lacorte, C. & Brasileiro, A.C.M. Evaluation of heterologous promoters in transgenic Populus tremula × P. alba plants. Biol Plant 50, 15–20 (2006). https://doi.org/10.1007/s10535-005-0069-7
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DOI: https://doi.org/10.1007/s10535-005-0069-7