Transgenic approaches to increase dehydration-stress tolerance in plants

Plant productivity is strongly influenced by abiotic stress conditions induced by drought, high salt and low temperature. Plants respond to these conditions with an array of biochemical and physiological adaptations, at least some of which are the result of changes in gene expression. Transgenic approaches offer a powerful means of gaining valuable information to better understand the mechanisms governing stress tolerance. They also offer new opportunities to improve dehydration-stress tolerance in crops by incorporating a gene involved in stress protection into species that lack them. In this review, we discuss progress made towards understanding the molecular elements involved in dehydration-stress responses that have been used to improve salt or drought tolerance following several transgenic approaches. Further, we discuss various strategies being used to produce transgenic plants with increased tolerance to dehydration stress. These include the overproduction of enzymes responsible for biosynthesis of osmolytes, late-embryogenesis-abundant proteins and detoxification enzymes. At this time, there is a need for a careful appraisal of the genes to be selected and promoter elements to be used, because constitutive expression of these genes may not be desirable in all applications. In this context, the advantages and limitations of transgenic approaches currently being used are discussed together with the importance of using stress-inducible promoters and the introduction of multiple genes for the improvement of dehydration-stress tolerance.     

Tobacco matrix attachment region sequence increased transgene expression levels in rice plants

In this study, six plasmids were constructed to study the effects of the tobacco Rb7 matrix attachment region (MAR) sequence on rice transgene expression. Among them, each of four plasmids contained two identical copies of the MAR sequence flanking two different reporter genes, which encode the green fluorescent protein and -glucuronidase. Two control plasmids contained no MAR sequences. Microprojectile bombardment was used to separately introduce these six plasmids into rice calli. Transgenic rice plants were regenerated, and gene expression was measured in rice leaf extracts of two-month-old transgenic plants. By comparing transgenic plants with the corresponding control plants, transgenic plants harboring each of four plasmids that included the MAR sequence resulted in average gene expression levels enhanced by 3.3-fold, 18-fold, 376-fold and 650-fold. These results suggest that the same MAR sequence can affect the expression of different genes to different extents. One goal of plant scientists and breeders is to maximize expression levels of transgenes, especially in the production of transgene-encoded protein. Therefore, inclusion of the Rb7 MAR sequence would be beneficial.     

Wheat LEA genes, PMA80 and PMA1959, enhance dehydration tolerance of transgenic rice (Oryza sativa L.)

Drought and salt stresses are two major factors that lower plant productivity. Transgenic approaches offer powerful means to better understand and then minimize loss of yield due to these abiotic stresses. In this study, we have generated transgenic rice plants expressing a wheat LEA group 2 protein (PMA80) gene, and separately the wheat LEA group 1 protein (PMA1959) gene. Molecular analysis of the transgenic plants revealed the stable integration of the transgenes. Immunoblot analysis showed the presence of the LEA group 2 protein (39 kDa) and the LEA group 1 protein (25 kDa) in most of the plant lines. Second-generation transgenic plants were subjected to dehydration or salt stress. The results showed that accumulation of either PMA80 or PMA1959 correlates with increased tolerance of transgenic rice plants to these stresses.