Method of enhancing plant resistance to geminiviruses by...

Multicellular living organisms and unmodified parts thereof and – Method of introducing a polynucleotide molecule into or... – The polynucleotide confers pathogen or pest resistance

Reexamination Certificate

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C800S278000, C800S306000, C800S298000, C800S295000, C800S320100, C800S320200, C800S320300, C800S320000, C800S317200, C800S317300, C800S312000

Reexamination Certificate

active

06777587

ABSTRACT:

BACKGROUND
Plant pathogens are of great economic importance, as plant disease accounts for a significant fraction of crop losses. The present invention provides a method of making plants with enhanced resistance to infection with plant pathogens, including viral pathogens, bacterial pathogens, and fungal pathogens.
SUMMARY OF THE INVENTION
The present invention provides a method of preparing plants with enhanced resistance to infection with plant pathogens. The method comprises transforming a plant cell with a DNA construct which comprises an exogenous SNF-1 transgene, i.e., a DNA which encodes an SNF-1 protein kinase or the catalytic domain of such kinase. The transgene also comprises a promoter which regulates expression of the SNF-1 kinase or the catalytic domain. The promoter is operably linked to the DNA sequence which encodes the SNF-1 kinase or catalytic domain. The method further comprises the step of generating a transformed plant from the transformed plant cell. The transformed plant expresses the SNF-1 kinase or the catalytic domain and, thus, contains an SNF-1 kinase or catalytic domain that is encoded by the SNF-1 transgene as well as the SNF-1 kinase that is encoded by the plants own SNF-1 gene. Such plants are referred to as “overexpressors.” The present method is especially useful for producing plants with enhanced resistance to plant pathogens, particularly viral pathogens, more particularly Geminiviruses. It is expected that the present method is also useful for producing plants with enhanced resistance to abiotic stress. Examples of abiotic stress are ozone, heat stress, and salt stress.
The present invention also provides a plant cell having a SNF-1 transgene stably integrated into its genome. The transgene comprises a DNA sequence encoding a SNF-1 kinase or the catalytic domain of such kinase and a promoter which controls expression of the DNA coding sequence in the plant cell. The present invention also relates to cell cultures consisting of such transformed cells, plants regenerated from such transformed cells and seeds of such transformed plants.


REFERENCES:
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Broun et al, Catalytic Plasticity of Fatty Acid Modification Enzymes Underlying Chemical Diversity of Plant Lipids, Nov. 1998, Science vol. 282, pp. 1315-1317.*
Lacombe et al, “The Identity of Plant Glutamate Receptors”, May 2001, Science vol. 292, pp. 1486-1487.*
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“Gene Regulation in Geminivirus” by Bisaro, International Workshop on Bemisia and Geminiviruses, San Jan, Puerto Rico, Jun. 7-12, 1998.
“The Role of Geminivirus Protein (TrAP) in Host Defence Suppression” by Bisaro, et al., The Thirteenth John Innes Symposium, Norfolk, UK, Jul. 20-23, 1999.
“Geminvirus Transactivator May Disable a Host Defense Response” by Bisaro, et al., 7thInternational Congress of Plant Pathology, Edinburgh, Scotland, Aug. 9-16, 1998.
“Structure and expression of a gene fromArabidopsis thalianaencoding a protein related to SNF1 protein kinase” by LeGuen, et al.,Gene, 120 (1992) 249-254.
“Regulatory interaction of PRL1 WD protein with Arabidopsis SNF1-like protein kinase” by Bhalerao, et al.,Proc. natl. Acad. Sci. USA, vol. 96, pp. 5323-5327, Apr. 1999.
“Two SNF1-Related Protein Kinases from Spinach Leaf Phosphorylate and Inactivate 1-Hydroxy-3-Methylgluataryl-Coenzyme A Reductase, Nitrate Reductase, and Sucrose Phosphate Synthase in Vitro” by Sugden, et al.,Plant Physiology, May 1999, vol. 120, pp. 257-274.

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