Multicellular living organisms and unmodified parts thereof and – Method of introducing a polynucleotide molecule into or...
Reexamination Certificate
1999-11-08
2004-11-30
Bui, Phuong T. (Department: 1638)
Multicellular living organisms and unmodified parts thereof and
Method of introducing a polynucleotide molecule into or...
C800S286000, C800S287000, C800S298000, C800S295000, C800S320000, C800S320100, C800S320300, C800S320200, C800S312000, C800S316000, C800S322000, C800S306000, C536S023600, C536S024100, C536S024500
Reexamination Certificate
active
06825397
ABSTRACT:
TECHNICAL FIELD
The present invention relates generally to plant molecular biology. More specifically, it relates to nucleic acids and methods for modulating their expression in plants.
BACKGROUND OF THE INVENTION
Major advances in plant transformation have occurred over the last few years. However, in major crop plants, such as maize and soybeans, serious genotype limitations still exist. Transformation of agronomically important maize inbred lines continues to be both difficult and time consuming. Traditionally, the only way to elicit a culture response has been by optimizing medium components and/or explant material and source. This has led to success in some genotypes, but most elite hybrids fail to produce a favorable culture response. While, transformation of model genotypes is efficient, the process of introgressing transgenes into production inbreds is laborious, expensive and time consuming. It would save considerable time and money if genes could be introduced into and evaluated directly in commercial hybrids.
Current methods for genetic engineering in maize require a specific cell type as the recipient of new DNA. These cells are found in relatively undifferentiated, rapidly growing callus cells or on the scutellar surface of the immature embryo (which gives rise to callus). Irrespective of the delivery method currently used, DNA is introduced into literally thousands of cells, yet transformants are recovered at frequencies of 10
−5
relative to transiently-expressing cells. Exacerbating this problem, the trauma that accompanies DNA introduction directs recipient cells into cell cycle arrest and accumulating evidence suggests that many of these cells are directed into apoptosis or programmed cell death. (Reference Bowen et al,
Third International Congress of the International Society for Plant Molecular Biology,
1991, Abstract 1093). Therefore it would be desirable to provide improved methods capable of increasing transformation efficiency in a number of cell types.
Typically a selectable marker is used to recover transformed cells. Traditional selection schemes expose all cells to a phytotoxic agent and rely on the introduction of a resistance gene to recover transformants. Unfortunately, the presence of dying cells may reduce the efficiency of stable transformation. It would therefore be useful to provide a positive selection system for recovering transformants.
In spite of increases in yield and harvested area worldwide, it is predicted that over the next ten years, meeting the demand for corn will require an additional 20% increase over current production (Dowswell, C. R., Paliwal, R. L., Cantrell, R. P., 1996, Maize in the Third World, Westview Press, Boulder, Colo.).
In hybrid crops, including grains, oil seeds, forages, fruits and vegetables, there are problems associated with the development and production of hybrid seeds. The process of cross-pollination of plants is laborious and expensive. In the cross-pollination process, the female plant must be prevented from being fertilized by its own pollen. Many methods have been developed over the years, such as detasseling in the case of corn, developing and maintaining male sterile lines, and developing plants that are incompatible with their own pollen, to name a few. Since hybrids do not breed true, the process must be repeated for the production of every hybrid seed lot.
To further complicate the process, inbred lines are crossed. For example in the case of corn, the inbreds can be low yielding. This provides a major challenge in the production of hybrid seed corn. In fact, certain hybrids cannot be commercialized at all due to the performance of the inbred lines. The production of hybrid seeds is consequently expensive, time consuming and provides known and unknown risks. It would therefore be valuable to develop new methods which contribute to the increase of production efficiency of hybrid seed.
As new traits are added to commercial crops by means of genetic engineering, problems arise in “stacking” traits. In order to develop heritable stacked traits, the traits must be linked because of segregating populations. Improved methods for developing hybrid seed which would not require linking of the traits would significantly shorten the time for developing commercial hybrid seeds.
Gene silencing is another problem in developing heritable traits with genetic engineering. Frequently gene silencing is seen following meiotic divisions. Elimination or reduction of this problem would advance the state of science and industry in this area.
SUMMARY OF THE INVENTION
It is the object of the present invention to provide nucleic acids and polypeptides relating to embryogenesis.
It is another object of the present invention to provide nucleic acids and polypeptides that can be used to identify interacting proteins involved in transcription regulation in embryogenesis.
It is another object of the present invention to provide antigenic fragments of the polypeptides of the present invention.
It is another object of the present invention to provide transgenic plants and plant parts containing the nucleic acids of the present invention.
It is another object of the present invention to provide methods for modulating, in a transgenic plant, the expression of the nucleic acids of the present invention.
It is another object of the present invention to provide a method for improving transformation frequencies.
It is another object of the present invention to provide a method for improving transformation efficiency in cells from various sources.
It is another object of the present invention to provide a method for a positive selection system.
It is another object of the present invention to provide a method for efficiently producing hybrid seed via apomixis.
It is another object of the present invention to provide a method for stacking traits which does not require linking of traits.
It is another object of the present invention to provide a method for reducing the problem of gene silencing.
The present invention relates to a HAP3-type CCAAT-box binding transcriptional activator polynucleotides and polypeptides, and in particular, the leafy cotyledon 1 transcriptional activator (LEC1) polynucleotides and polypeptides. In other aspects the present invention relates to expression cassettes optionally linked in antisense orientation, host cells transfected with at least one expression cassette, and transgenic plants and seeds comprising the expression cassettes. Further aspects of the invention include methods of using the polynucleotides and polypeptides. In a further aspect, the present invention relates to a method of modulating expression of the polynucleotides encoding the polypeptides of the present invention in a plant. Expression of the polynucleotides encoding the proteins of the present invention can be increased or decreased relative to a non-transformed control plant.
REFERENCES:
patent: 5811636 (1998-09-01), Hanna et al.
patent: 6235975 (2001-05-01), Harada et al.
patent: 6320102 (2001-11-01), Harada et al.
patent: WO 98/37184 (1998-08-01), None
patent: WO 99/67405 (1999-12-01), None
Sasaki, T. Acession No. C19737, p. 10, Deposited 1996.*
Kemp, DJ. Accession No. AAN60472, p. 13, Deposited 1991.*
Bork, “Powers and Pitfalls in Sequence Analysis: The 70% Hurdle”, No. 1998, vol. 10, pp. 398-400.*
Lazar et al, “Transforming Growth Factor x: Mutation of Aspartic Acid 47 and leucine 48 Results in Different Biological Activities”, Mar. 1998, Molecular and Cellular Biology, pp. 1247-1252.*
Sequence Search Result, Accession No. Y11210, 1997.*
Sasaki, T. ; AC C19737, “Rice cDNA from panicle at ripning stage”, EBI Database, Oct. 25, 1996 (XP002136426).
Sasaki, T.; AC C28028, Rice cDNA from callus (970724.1345), EBI Database, Aug. 6, 1997 (XP002136427).
West et al., “Leafy Cotyledoni is an Essential Regulator of Late Embryogenesis and Cotyledon Identity in Arabidopis”,The Plant Cell, 6(12):1731-1745, 1994.
Parcy et al., “The Abscisic Acid-Insensitive3, Fusca3 and Leafy Cotyledon1 Loci Act in Concert to Control Multiple Aspect
Cahoon Rebecca E.
Gordon-Kamm William J.
Gregory Carolyn A.
Hoerster George J.
Klein Theodore M.
Bui Phuong T.
Ibrahim Medina A.
Pioneer Hi-Bred International , Inc.
Pioneer Hi-Bred International Inc.
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