Chemistry: molecular biology and microbiology – Process of mutation – cell fusion – or genetic modification – Introduction of a polynucleotide molecule into or...
Reexamination Certificate
1999-10-12
2001-10-02
McElwain, Elizabeth F. (Department: 1638)
Chemistry: molecular biology and microbiology
Process of mutation, cell fusion, or genetic modification
Introduction of a polynucleotide molecule into or...
C800S306000, C435S419000, C435S420000, C435S430100, C435S470000
Reexamination Certificate
active
06297056
ABSTRACT:
FIELD OF THE INVENTION
The field of the invention relates to the genetic engineering of plants, particularly methods for genetically transforming Brassica plants.
BACKGROUND OF THE INVENTION
Among the genera of cruciferous plants, the majority of the species cultivated by man are from the genus Brassica. Plants from this genus are used as a source of vegetables, condiments, vegetable oil and animal feeds. Some Brassica plants that are used for vegetable production include cabbage, cauliflower, broccoli, kale, kohlrabi, leaf mustard and rutabaga. Seeds of
B. hirta
are used to produce the popular American condiment, yellow mustard. However, on a world-wide basis, the most economically important use of Brassica species is for the production of seed-derived, vegetable oils. The predominant Brassica species grown for oil production is
B. napus.
Seeds of
B. napus
are referred to as rapeseed. Seeds of other Brassica species, particularly those grown for seed oil production, are also often referred to as rapeseed. Brassica species that are grown primarily for oil production are often called oilseed rape. In North America, canola, a type of oilseed rape that has been selected for low levels of erucic acid and glucosinolates in seeds, is the predominant Brassica plant grown for the production of vegetable oil for human consumption. While low-erucic-acid rapeseed oils, such as canola oil, may be favored for human consumption, high-erucic-acid rapeseed oils are desirable for a variety of industrial applications including the production of cosmetics, lubricants, plasticizers and surfactants.
Because of the agricultural and industrial importance of plants from the genus Brassica, plant breeders are working to develop new varieties with improved agronomic characteristics. While traditional breeding approaches are certainly important, significant improvements in cultivated Brassica varieties have been made recently through the introduction of recombinant DNA into the Brassica genome by genetic transformation methods. A number of genetically modified Brassica varieties have already reached farmers' fields in North America. Transgenic canola varieties, genetically modified for resistance to herbicides, have rapidly gained favor with agricultural producers across the canola-growing regions of the United States and Canada. The phenomenal success of the transgenic canola varieties in North America has led to an acceleration in the development of new transgenic varieties of canola. Novel, recombinant DNA-based strategies for incorporating new traits, such as disease and insect resistance, modified seed oil composition and modified seed protein composition, are being developed for canola and other Brassica species. All of the these strategies depend on genetic transformation methods to introduce the recombinant DNA into the genomes of Brassica plants.
Currently, the most favored methods for transforming Brassica species involve the use of Agrobacterium. While the Agrobacterium-based transformation methods provide a reliable means for introducing foreign DNA into dicots, there are a number of disadvantages to methods of plant transformation that involve the use of Agrobacterium. First, an undesired consequence of all Agrobacterium-based methods is the introduction of at least one T-DNA border into the genome of the recipient plant. While the T-DNA border is an essential element of the genetic mechanism by which Agrobacterium transfers DNA to a plant cell, the T-DNA border is not essential for the expression foreign genes in the recipient plant. Additionally, the accumulation of multiple T-DNA borders throughout the genome of a plant may have deleterious effects on the plant or its progeny. Second, the co-cultivation of plant tissues with Agrobacterium may slow the regeneration of a transformed plant from a transformed cell. After the co-cultivation phase, Agrobacterium must be eliminated from cultures of the plant tissues. High levels of bactericidal agents must be applied to the plant cultures to kill the Agrobacterium. While the levels of bactericidal agents applied to the cultures are generally not lethal to the plant tissues, the presence of the bactericidal agents in the cultures may negatively impact plant growth and thus, slow the regeneration of transformed plants. Third, prior to DNA transfer to a plant, natural genetic processes might occur in Agrobacterium such as genetic recombination and DNA rearrangements that may have undesired effects on the DNA fragment that is transferred to the plant. Such undesired effects may alter or eliminate the intended genetic function of the introduced DNA fragment.
Efficient Brassica transformation methods that do not involve the use of Agrobacterium are desired. While non-Agrobacterium-based, Brassica transformation methods have been reported, the efficiency of such methods, in general, has been insufficient for routine use in commercial Brassica improvement programs. To meet the increasing demands of agriculture in the world today, the pace of development of new transgenic varieties of canola and other Brassica species must be accelerated. Increasing the pace of Brassica variety development depends on the availability of reliable and efficient methods for the transformation and regeneration of transformed Brassica plants.
SUMMARY OF THE INVENTION
Methods are provided for producing transgenic Brassica plants. The methods find use in agriculture, particularly in the development of improved varieties of Brassica plants through the incorporation of new agronomic traits. The methods involve introducing a DNA construct by microprojectile bombardment into a Brassica cell that is capable of regenerating into a fertile, stably transformed Brassica plant and regenerating such a Brassica plant from the cell.
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Chen et al. 1994. A combined use of microprojectile bombardment and DNA imbibition enhances transformation frequency of canola (Brassica napusL.). Theor. App. Genet. 88:187-192.*
Loh et al. 1983. Cytokinins and the regeneration of plantlets from secondary embryoids of winter oilseed rape,Brassica napusssp.oleifera. New Phytol. vol. 95:349-358.*
Moloney et al., High Efficiency Transformation ofBassica NapusUsing Agrobacterium Vectors, Plant Cell Reports, 1989, pp. 238-242, vol. 8.
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Arnoldo MaryAnne
Bower Michael S.
Burnett Laurie A.
Ide Christine L.
Le Mai N.
Alston & Bird LLP
Collins Cynthia
McElwain Elizabeth F.
Pioneer Hi-Bred International , Inc.
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