US20120144520A1

US20120144520A1 - Plants with Improved Nitrogen Utilization and Stress Tolerance

Info

Publication number: US20120144520A1
Application number: US13/309,308
Authority: US
Inventors: James McLaren; Nicholas Duck; Brian Vande Berg; Alissa Schawalder; Vadim Beilinson; Jill Hinson
Original assignee: Iowa Corn Promotion Board
Current assignee: Iowa Corn Promotion Board
Priority date: 2006-10-27
Filing date: 2011-12-01
Publication date: 2012-06-07
Also published as: US9416367B2; EP2094076A2; WO2008051608A2; WO2008051608A8; BRPI0718276A2; EP2976941A1; CA2667558A1; EP2094076A4; US20150096077A1; US20100162433A1; ZA200902879B; CN101626680B; CN103773800A; CN101626680A

Abstract

The present invention relates to transgenic plants that have increased nitrogen use efficiency, stress tolerance, or both and that have been transformed using a novel vector construct including nucleic acid sequences that modulate nitrogen use in plants. In various embodiments, the vector construct comprises a nucleic acid sequence selected from the group consisting of SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, or 38. The invention also relates to isolated vectors for transforming plants and to antibodies used for detecting transformed plants. The invention also relates to methods of expressing in plants the nucleic acid molecules corresponding to the nucleic acid sequences that modulate nitrogen use in plants or are modulated by nitrogen conditions.

Description

This application claims priority to U.S. application Ser. No. 11/977,768, filed Oct. 26, 2007, which claims priority to U.S. Application Ser. No. 60/854,927, filed Oct. 27, 2006, which is incorporated herein in its entirety by this reference.

BACKGROUND OF THE INVENTION

The invention relates generally to plants with improved nitrogen utilization and stress tolerance, more specifically, to corn plants transformed with a gene that improves stress tolerance and nitrogen uptake, metabolism or both.
Plants require nitrogen during their vegetative and reproductive growth phases. Nitrogen is made available to the plant through soil mineralization, the application of nitrogen fertilizer, or both. It has been estimated, however, that between 50 and 70 percent of nitrogen applied to crops is lost from the plant-soil system [Peoples, M. B. et al., “Minimizing Gaseous Losses of Nitrogen,” In Nitrogen Fertilizer in the Environment (Bacon, P. E., ed.) Marcel Dekker, pp. 565-606 (1995)]. Nitrogen is one of the most expensive plant nutrients to supply, nitrogen fertilizer is not always available at a reasonable cost, and excessive application of nitrogen fertilizer can result in pollution problems in runoff. Corn is an example of an agronomically important plant that often requires nitrogen fertilizers to perform at its genetic potential.
The development of plant varieties that use nitrogen more efficiently will reduce the need for excessive inputs of nitrogen, save production costs for farmers, benefit farmers in developing countries who do not have access to fertilizer inputs, and reduce pollution associated with the application of excessive nitrogen fertilizers. One approach that has been used in the development of plant varieties with improved nitrogen utilization relies on conventional plant breeding techniques. An alternative approach that may be more efficient would use genetic engineering to attempt to transform plants by the introduction of genes that have been identified by various groups as having a potential impact on nitrogen uptake and use.

SUMMARY OF THE INVENTION

The present invention relates to transgenic plants that have increased nitrogen use efficiency, stress tolerance, or both, that have been transformed using a novel vector construct including nucleic acid sequences that modulate nitrogen use in plants. The invention also relates to isolated vectors for transforming plants and to antibodies for detecting expression of the nucleotide sequence of interest in the transformed plants. The invention also relates to methods of expressing in plants the nucleic acid molecules corresponding to the nucleic acid sequences that modulate nitrogen use in plants.
Specifically, vectors for transforming plants have been constructed using nucleotide sequences selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, and SEQ ID NO: 38, as well as variants, fragments, and complements thereof. These vectors include a 5′ DNA promoter sequence and a 3′ terminator sequence, wherein the nucleic acid sequence, the DNA promoter sequence, and the terminator sequence are operatively coupled to permit transcription of the nucleotide sequence. The promoter sequence may be a constitutive plant promoter or a tissue specific promoter.
The invention also includes polyclonal antibodies, comprising polyclonal antibodies to a nucleotide sequence selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36; and SEQ ID NO: 38.
The invention also includes a novel methodology for assaying nitrogen use efficiency.
The invention also includes plants transformed with nucleotide sequences selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, and SEQ ID NO: 38, as well as variants and fragments thereof. The plant is selected from the group consisting of rice, corn, soybean, canola, wheat, alfalfa, barley, rye, cotton, sunflower, peanut, sweet potato, bean, pea, potato, oilseed rape, sorghum, forage grass, pasture grass, turf grass, and sugarcane. The invention also includes a component part of such plants, plant seed produced from such plants, and a plant seed transformed with a vector construct of the present invention.
The invention also includes a host cell transformed with a nucleotide sequence selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36; and SEQ ID NO: 38. The host cell may be a bacterial cell or a plant cell.
The invention also includes a method of expressing a nucleic acid molecule modulated by nitrogen in a plant, said method comprising the steps of providing a transgenic plant or plant seed transformed with a vector construct according to the present invention, and growing the transgenic plant or a plant grown from the transgenic plant seed under conditions effective to express the nucleic acid molecule in said transgenic plant or said plant grown from the transgenic plant seed. Growing of the transgenic plant is effective in reducing nitrogen uptake of said transgenic plant or said plant grown from the transgenic plant seed, in increasing nitrogen uptake of said transgenic plant or said plant grown from the transgenic plant seed, and in increasing efficiency of nitrogen utilization of said transgenic plant or said plant grown from the transgenic plant seed. The invention also includes the foregoing methods wherein a transgenic plant is provided or a transgenic seed is provided. The invention also includes the foregoing method wherein the plant is selected from the group consisting of rice, corn, soybean, canola, wheat, alfalfa, barley, rye, cotton, sunflower, peanut, sweet potato, bean, pea, potato, oilseed rape, sorghum, forage grass, pasture grass, turf grass, sugarcane.
The invention also includes a method of improving the stress tolerance of a plant by expressing a nucleic acid molecule modulated by nitrogen in a plant, said method comprising the steps of providing a transgenic plant or plant seed transformed with a vector construct according to the present invention and growing the transgenic plant or a plant grown from the transgenic plant seed under conditions effective to express the nucleic acid molecule in said transgenic plant or said plant grown from the transgenic plant seed.
The invention also includes a method of altering the morphology of a plant by expressing a nucleic acid molecule modulated by nitrogen in a plant, said method comprising the steps of providing a transgenic plant or plant seed transformed with a vector construct according to the present invention and growing the transgenic plant or a plant grown from the transgenic plant seed under conditions effective to express the nucleic acid molecule in said transgenic plant or said plant grown from the transgenic plant seed.
The invention also includes a vector construct, comprising a nucleotide sequence encoding an amino acid sequence selected from the list consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37 and SEQ ID NO: 37, a 5′ DNA promoter sequence, and a 3′ terminator sequence, wherein the nucleotide sequence, the DNA promoter sequence, and the terminator sequence are operatively coupled to permit transcription of the nucleotide sequence.
The invention also includes a vector construct comprising a nucleotide sequence that is modulated by nitrogen in a plant, wherein said nucleotide sequence is selected from the group consisting of a nucleotide sequence selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36; and SEQ ID NO: 38, and a nucleotide sequence encoding an amino acid sequence selected from the list consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37 and SEQ ID NO: 39, wherein said construct further comprises a 5′ DNA promoter sequence and a 3′ terminator sequence, wherein the nucleotide sequence, the DNA promoter sequence, and the terminator sequence are operatively coupled to permit transcription of the nucleotide sequence.
The invention also includes a vector construct comprising a nucleotide sequence that is modulated by nitrogen in a plant, wherein said nucleotide sequence is selected from the group consisting of a nucleotide sequence selected from the list consisting of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, and SEQ ID NO: 38, a nucleotide sequence having at least 95% sequence identity to the nucleotide sequence of SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 13, SEQ ID NO: 15, SEQ ID NO: 17, SEQ ID NO: 22, SEQ ID NO: 24, SEQ ID NO: 26, SEQ ID NO: 28, SEQ ID NO: 30, SEQ ID NO: 32, SEQ ID NO: 34, SEQ ID NO: 36, or SEQ ID NO: 38, wherein said nucleotide sequence is modulated by nitrogen in a plant, and a nucleotide sequence encoding an amino acid sequence selected from the list consisting of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, and SEQ ID NO: 39, and a nucleotide sequence encoding an amino acid sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 14, SEQ ID NO: 16, SEQ ID NO: 18, SEQ ID NO: 23, SEQ ID NO: 25, SEQ ID NO: 27, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 33, SEQ ID NO: 35, SEQ ID NO: 37, or SEQ ID NO: 39, wherein said nucleotide sequence is modulated by nitrogen in a plant, wherein said construct further comprises a 5′ DNA promoter sequence and a 3′ terminator sequence, wherein the nucleotide sequence, the DNA promoter sequence, and the terminator sequence are operatively coupled to permit transcription of the nucleotide sequence.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

There is a need to develop plant cultivars that absorb and use nitrogen more efficiently. Plant scientists have adopted the shorthand term nitrogen use efficiency (NUE), and a variety of methods of measuring and evaluating NUE have been developed [Craswell, E. T. and Godwin, D. C. (1984) The efficiency of nitrogen fertilizers applied to cereals grown in different climates. In Advances in Plant Nutrition (Vol. 1) (Tinker, P. B. and Lauchli, A., eds), pp. 1-55, Praeger Publishers; Steenbjerg, F. and Jakobsen, S. T. (1963) Plant nutrition and yield curves. Soil Sci. 95, 69-90; Siddiqi, M. Y. and Glass, D. M. (1981) Utilization index: a modified approach to the estimation and comparison of nutrient utilization efficiency in plants. J. Plant Nutr. 4, 289-302; Moll, R. H. et al. (1982) Analysis and interpretation of factors which contribute to efficiency of nitrogen utilization. Agron. J. 74, 562-564]. There are differences in the definitions. Some definitions are based on total biomass while others are based on the weight of grain yielded. Another set of definitions uses the efficiency of extracting nitrogen from the soil. The efficiency with which applied nitrogen is used to improve grain yield may be measured by agronomic efficiency (AE), the product of physiological efficiency and utilization efficiency, or NUEg which is the product of uptake efficiency and utilization efficiency. Other definitions take physiological factors into account.
As used in this specification, the term nitrogen use efficiency, or NUE, is defined to include a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (for example, may include a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, chlorophyll content), or where the plant is shown to provide the same or elevated yield at lower nitrogen fertilization levels, or where the plant is shown to provide elevated yields at the same nitrogen fertilization levels when compared to a plant that has not been transformed with an nitrogen-modulated nucleic acid construct of the invention. A “measurable change” can include an increase or a decrease in the amount of any component (“metabolic pool”) of the nitrogen assimilation pathway. A change can include either a decrease or an increase in one or more metabolic pools in the pathway, or a decrease in one or more pools with a concomitant increase in one or more other pool(s). For example, the level of one pool (e.g., glutamate) can decrease while the level of another pool (e.g., glutamine) can increase.
An increase in nitrogen utilization efficiency can be associated with about a 5%, about a 10%, 15%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 125%, 150%, about a 200% or greater measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathway. In one embodiment, the transgenic plants of the invention have an increased nitrogen uptake from the environment when compared to a plant that does not contain a nitrogen-modulated sequence of the invention. In another embodiment, the transgenic plants of the invention have a decreased nitrogen uptake from the environment when compared to a plant that does not contain a nitrogen-modulated sequence of the invention. By “nitrogen modulating sequence” is intended a nucleotide or amino acid sequence that is modulated (e.g., increased or decreased, or upregulated or downregulated) in response to exposure to nitrogen.
The present invention further provides a method of improving stress tolerance in a plant by expressing a nitrogen-modulated nucleotide sequence within the plant. In one embodiment, the nitrogen-modulated nucleotide sequence is SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, or 38, or variants and fragments thereof. In another embodiment, the nitrogen-modulated nucleotide sequence is a nucleotide sequence that encodes SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, or 39, or variants and fragments thereof.
As used herein, the term “stress” or “stress condition” refers to the exposure of a plant, plant cell, or the like, to a physical or chemical agent or condition that has an adverse effect on metabolism, growth, development, propagation and/or survival of the plant (collectively “growth”). A stress can be imposed on a plant due, for example, to an environmental factor such as water (e.g., flooding, drought, dehydration), anaerobic conditions (e.g., a low level of oxygen), abnormal osmotic conditions, salinity or temperature (e.g., hot/heat, cold, freezing, frost), a deficiency of nutrients such as nitrogen or exposure to pollutants, or by a hormone, second messenger or other molecule. Anaerobic stress, for example, is due to a reduction in oxygen levels (hypoxia or anoxia) sufficient to produce a stress response. A flooding stress can be due to prolonged or transient immersion of a plant, plant part, tissue or isolated cell in a liquid medium such as occurs during monsoon, wet season, flash flooding or excessive irrigation of plants, or the like. A cold stress or heat stress can occur due to a decrease or increase, respectively, in the temperature from the optimum range of growth temperatures for a particular plant species. Such optimum growth temperature ranges are readily determined or known to those skilled in the art. Dehydration stress can be induced by the loss of water, reduced turgor, or reduced water content of a cell, tissue, organ or whole plant. Drought stress can be induced by or associated with the deprivation of water or reduced supply of water to a cell, tissue, organ or organism. Saline stress (salt stress) can be associated with or induced by a perturbation in the osmotic potential of the intracellular or extracellular environment of a cell. Osmotic stress also can be associated with or induced by a change, for example, in the concentration of molecules in the intracellular or extracellular environment of a plant cell, particularly where the molecules cannot be partitioned across the plant cell membrane.
Transformation of Bacterial or Plant Cells
Provided herein are novel nucleotide sequences that modulate nitrogen utilization efficiency in plants. Also provided are amino acid sequences of the nitrogen-modulated proteins of the invention.
The nitrogen-modulated nucleotide sequences of the invention may be modified to obtain or enhance expression in plant cells. The nitrogen-modulated sequences of the invention may be provided in expression cassettes for expression in the plant of interest. “Plant expression cassette” includes DNA constructs that are capable of resulting in the expression of a protein from an open reading frame in a plant cell. The cassette will include in the 5′-3′ direction of transcription, a transcriptional initiation region (i.e., promoter) operably-linked to a DNA sequence of the invention, and a transcriptional and translational termination region (i.e., termination region) functional in plants. The cassette may additionally contain at least one additional gene to be cotransformed into the organism, such as a selectable marker gene. Alternatively, the additional gene(s) can be provided on multiple expression cassettes. Such an expression cassette is provided with a plurality of restriction sites for insertion of the nitrogen-modulated sequence to be under the transcriptional regulation of the regulatory regions.
By “promoter” is intended a nucleic acid sequence that functions to direct transcription of a downstream coding sequence. The promoter, together with other transcriptional and translational regulatory nucleic acid sequences (also termed as “control sequences”), are necessary for the expression of a DNA sequence of interest. Preferably, the promoter is one that is known to stimulate transcription in the organism into which the nucleotide sequence of the invention is being introduced.
The promoter may be native or analogous, or foreign or heterologous, to the plant host and/or to the DNA sequence of the invention. Additionally, the promoter may be the natural sequence or alternatively a synthetic sequence. Where the promoter is “native” or “homologous” to the plant host, it is intended that the promoter is found in the native plant into which the promoter is introduced. Where the promoter is “foreign” or “heterologous” to the DNA sequence of the invention, it is intended that the promoter is not the native or naturally occurring promoter for the operably linked DNA sequence of the invention. “Heterologous” generally refers to the nucleic acid sequences that are not endogenous to the cell or part of the native genome in which they are present, and have been added to the cell by infection, transfection, microinjection, electroporation, microprojection, or the like. By “operably linked” is intended a functional linkage between a promoter and a second sequence, wherein the promoter sequence initiates and mediates transcription of the DNA sequence corresponding to the second sequence. Generally, “operably linked” means that the nucleic acid sequences being linked are contiguous and, where necessary to join two protein coding regions, contiguous and in the same reading frame.
In one embodiment, the promoter is a constitutive promoter. Suitable constitutive promoters for use in plants include: the promoters from plant viruses, such as the peanut chlorotic streak caulimovirus (PC1SV) promoter (U.S. Pat. No. 5,850,019); the 35S promoter from cauliflower mosaic virus (CaMV) (Odell et al. (1985) Nature 313:810-812); promoters of Chlorella virus methyltransferase genes (U.S. Pat. No. 5,563,328) and the full-length transcript promoter from figwort mosaic virus (FMV) (U.S. Pat. No. 5,378,619); the promoters from such genes as rice actin (McElroy et al. (1990) Plant Cell 2:163-171); ubiquitin (Christensen et al. (1989) Plant Mol. Biol. 12:619-632 and Christensen et al. (1992) Plant Mol. Biol. 18:675-689), including the TrpPro5 promoter (U.S. patent application Ser. No. 10/377,318; filed Mar. 16, 2005); pEMU (Last et al. (1991) Theor. Appl. Genet. 81:581-588); MAS (Velten et al. (1984) EMBO J. 3:2723-2730); maize H3 histone (Lepetit et al. (1992) Mol. Gen. Genet. 231:276-285 and Atanassova et al. (1992) Plant J. 2(3):291-300); Brassica napus ALS3 (PCT application WO 97/41228); and promoters of various Agrobacterium genes (see U.S. Pat. Nos. 4,771,002; 5,102,796; 5,182,200; and 5,428,147).
In another embodiment, the promoter is a tissue-specific promoter. A list of commonly-used tissue-specific promoters can be found in Reviewed in Moore et al. (2006) Plant J. 45(4):651-683, which is herein incorporated by reference in its entirety.
Often, such constructs will also contain 5′ and 3′ untranslated regions. Such constructs may contain a “signal sequence” or “leader sequence” to facilitate co-translational or post-translational transport of the peptide of interest to certain intracellular structures such as the chloroplast (or other plastid), endoplasmic reticulum, or Golgi apparatus, or to be secreted. For example, the gene can be engineered to contain a signal peptide to facilitate transfer of the peptide to the endoplasmic reticulum. By “signal sequence” is intended a sequence that is known or suspected to result in cotranslational or post-translational peptide transport across the cell membrane. In eukaryotes, this typically involves secretion into the Golgi apparatus, with some resulting glycosylation. By “leader sequence” is intended any sequence that when translated, results in an amino acid sequence sufficient to trigger co-translational transport of the peptide chain to a sub-cellular organelle. Thus, this includes leader sequences targeting transport and/or glycosylation by passage into the endoplasmic reticulum, passage to vacuoles, plastids including chloroplasts, mitochondria, and the like. It may also be preferable to engineer the plant expression cassette to contain an intron, such that mRNA processing of the intron is required for expression.
By “3′ untranslated region” is intended a nucleotide sequence located downstream of a coding sequence. Polyadenylation signal sequences and other sequences encoding regulatory signals capable of affecting the addition of polyadenylic acid tracts to the 3′ end of the mRNA precursor are 3′ untranslated regions. By “5′ untranslated region” is intended a nucleotide sequence located upstream of a coding sequence.
Other upstream or downstream untranslated elements include enhancers. Enhancers are nucleotide sequences that act to increase the expression of a promoter region. Enhancers are well known in the art and include, but are not limited to, the SV40 enhancer region and the 35S enhancer element.
The termination region may be native with the transcriptional initiation region, may be native with the nitrogen-modulated sequence of the present invention, or may be derived from another source. Convenient termination regions are available from the Ti-plasmid of A. tumefaciens, such as the octopine synthase and nopaline synthase termination regions, or the potato proteinase inhibitor II sequence (PinII) as described in Liu et al. (2004) Acta Biochim Biophys Sin 36(8):553-558. See also Guerineau et al. (1991) Mol. Gen. Genet. 262:141-144; Proudfoot (1991) Cell 64:671-674; Sanfacon et al. (1991) Genes Dev. 5:141-149; Mogen et al. (1990) Plant Cell 2:1261-1272; Munroe et al. (1990) Gene 91:151-158; Ballas et al. (1989) Nucleic Acids Res. 17:7891-7903; and Joshi et al. (1987) Nucleic Acid Res. 15:9627-9639.
Where appropriate, the gene(s) may be optimized for increased expression in the transformed host cell. That is, the genes can be synthesized using host cell-preferred codons for improved expression, or may be synthesized using codons at a host-preferred codon usage frequency. Generally, the GC content of the gene will be increased. See, for example, Campbell and Gowri (1990) Plant Physiol. 92:1-11 for a discussion of host-preferred codon usage. Methods are known in the art for synthesizing host-preferred genes. See, for example, U.S. Pat. Nos. 6,320,100; 6,075,185; 5,380,831; and 5,436,391, U.S. Published Application Nos. 20040005600 and 20010003849, and Murray et al. (1989) Nucleic Acids Res. 17:477-498, herein incorporated by reference.
In one embodiment, the nucleic acids of interest are targeted to the chloroplast for expression. In this manner, where the nucleic acid of interest is not directly inserted into the chloroplast, the expression cassette will additionally contain a nucleic acid encoding a transit peptide to direct the gene product of interest to the chloroplasts. Such transit peptides are known in the art. See, for example, Von Heijne et al. (1991) Plant Mol. Biol. Rep. 9:104-126; Clark et al. (1989) J. Biol. Chem. 264:17544-17550; Della-Cioppa et al. (1987) Plant Physiol. 84:965-968; Romer et al. (1993) Biochem. Biophys. Res. Commun. 196:1414-1421; and Shah et al. (1986) Science 233:478-481.
The nucleic acids of interest to be targeted to the chloroplast may be optimized for expression in the chloroplast to account for differences in codon usage between the plant nucleus and this organelle. In this manner, the nucleic acids of interest may be synthesized using chloroplast-preferred codons. See, for example, U.S. Pat. No. 5,380,831, herein incorporated by reference.
Typically this “plant expression cassette” will be inserted into a “plant transformation vector.” By “transformation vector” is intended a DNA molecule that is necessary for efficient transformation of a cell. Such a molecule may consist of one or more expression cassettes, and may be organized into more than one “vector” DNA molecule. For example, binary vectors are plant transformation vectors that utilize two non-contiguous DNA vectors to encode all requisite cis- and trans-acting functions for transformation of plant cells (Hellens and Mullineaux (2000) Trends in Plant Science 5:446-451). “Vector” refers to a nucleic acid construct designed for transfer between different host cells. “Expression vector” refers to a vector that has the ability to incorporate, integrate and express heterologous DNA sequences or fragments in a foreign cell.
This plant transformation vector may be comprised of one or more DNA vectors needed for achieving plant transformation. For example, it is a common practice in the art to utilize plant transformation vectors that are comprised of more than one contiguous DNA segment. These vectors are often referred to in the art as “binary vectors.” Binary vectors as well as vectors with helper plasmids are most often used for Agrobacterium-mediated transformation, where the size and complexity of DNA segments needed to achieve efficient transformation is quite large, and it is advantageous to separate functions onto separate DNA molecules. Binary vectors typically contain a plasmid vector that contains the cis-acting sequences required for T-DNA transfer (such as left border and right border), a selectable marker that is engineered to be capable of expression in a plant cell, and a “nucleotide sequence of interest” (a nucleotide sequence engineered to be capable of expression in a plant cell for which generation of transgenic plants is desired). Also present on this plasmid vector are sequences required for bacterial replication. The cis-acting sequences are arranged in a fashion to allow efficient transfer into plant cells and expression therein. For example, the selectable marker gene and the gene of interest are located between the left and right borders. Often a second plasmid vector contains the trans-acting factors that mediate T-DNA transfer from Agrobacterium to plant cells. This plasmid often contains the virulence functions (Vir genes) that allow infection of plant cells by Agrobacterium, and transfer of DNA by cleavage at border sequences and vir-mediated DNA transfer, as is understood in the art (Hellens and Mullineaux (2000) Trends in Plant Science, 5:446-451). Several types of Agrobacterium strains (e.g. LBA4404, GV3101, EHA101, EHA105, etc.) can be used for plant transformation. The second plasmid vector is not necessary for transforming the plants by other methods such as microprojection, microinjection, electroporation, polyethylene glycol, etc.
Altered or Improved Variants Useful in the Constructs of the Invention
It is recognized that nucleotide and amino acid sequences useful in the present invention may be altered by various methods, and that these alterations may result in sequences encoding proteins with amino acid sequences different than that encoded by the nitrogen-modulated sequences disclosed herein.
Nucleotide sequences useful in the present invention include the sequences set forth in SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, and 38, and variants, fragments, and complements thereof. As used herein, the term “nucleotide sequence” or “nucleic acid molecule” is intended to include DNA molecules (e.g., cDNA or genomic DNA) and RNA molecules (e.g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs. The nucleic acid molecules can be single-stranded or double-stranded, but preferably are double-stranded DNA. By “complement” is intended a nucleotide sequence that is sufficiently complementary to a given nucleotide sequence such that it can hybridize to the given nucleotide sequence to thereby form a stable duplex. The corresponding amino acid sequences for the nitrogen-modulated proteins encoded by these nucleotide sequences are set forth in SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, and 39, as well as variants and fragments thereof. The invention also encompasses the use of nucleic acid molecules comprising nucleotide sequences encoding partial-length nitrogen-modulated proteins, and complements thereof.
Nucleic acid molecules that are fragments of these nitrogen-modulated nucleotide sequences are also useful in the present invention. By “fragment” is intended a portion of a nucleotide sequence encoding a nitrogen-modulated protein. A fragment of a nucleotide sequence may encode a biologically active portion of a nitrogen-modulated protein, or it may be a fragment that can be used as a hybridization probe or PCR primer using methods disclosed below. Nucleic acid molecules that are fragments of a nitrogen-modulated nucleotide sequence comprise at least about 15, 20, 50, 75, 100, 200, 300, 350, or at least about 400 contiguous nucleotides, or up to the number of nucleotides present in a full-length nitrogen-modulated nucleotide sequence disclosed herein depending upon the intended use. By “contiguous” nucleotides is intended nucleotide residues that are immediately adjacent to one another.
Polypeptides that are fragments of these nitrogen-modulated polypeptides are also useful in the present invention. By “fragment” is intended a portion of an amino acid sequence encoding a nitrogen-modulated protein as set forth SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, or 39, and that retains nitrogen utilization efficiency. A biologically active portion of a nitrogen-modulated protein can be a polypeptide that is, for example, 10, 25, 50, 100, 125, 150, 175, 200, 250, 300, 350, 400 or more amino acids in length. Such biologically active portions can be prepared by recombinant techniques and evaluated for nitrogen utilization efficiency. As used here, a fragment comprises at least 8 contiguous amino acids of SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, or 39. The invention encompasses other fragments, however, such as any fragment in the protein greater than about 10, 20, 30, 50, 100, 150, 200, 250, 300, 350, or 400 amino acids.
The invention also encompasses the use of variant nucleic acid molecules, or variant amino acid sequences, in the methods and compositions of the inventions. “Variants” of the nitrogen-modulated nucleotide sequences include those sequences that encode a nitrogen-modulated protein disclosed herein but that differ conservatively because of the degeneracy of the genetic code, as well as those that are sufficiently identical as discussed above. Naturally occurring allelic variants can be identified with the use of well-known molecular biology techniques, such as polymerase chain reaction (PCR) and hybridization techniques as outlined below. Variant nucleotide sequences also include synthetically derived nucleotide sequences that have been generated, for example, by using site-directed mutagenesis but which still encode the nitrogen-modulated proteins disclosed in the present invention as discussed below. Variant proteins useful in the present invention are biologically active, that is they retain the desired biological activity of the native protein, that is, nitrogen utilization efficiency.
By “variants” is intended proteins or polypeptides having an amino acid sequence that is at least about 60%, 65%, about 70%, 75%, 80%, 85%, or 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% identical to the amino acid sequence of SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, or 39. Variants also include polypeptides encoded by a nucleic acid molecule that hybridizes to the nucleic acid molecule of SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, or 38, or a complement thereof, under stringent conditions. Variants include polypeptides that differ in amino acid sequence due to mutagenesis. Variant proteins encompassed by the present invention are biologically active, that is they continue to possess the desired biological activity of the native protein, that is, retain nitrogen utilization efficiency.
Preferred nitrogen-modulated proteins useful in the present invention are encoded by a nucleotide sequence sufficiently identical to the nucleotide sequence of SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, or 38. The term “sufficiently identical” is intended an amino acid or nucleotide sequence that has at least about 60% or 65% sequence identity, about 70% or 75% sequence identity, about 80% or 85% sequence identity, or about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity compared to a reference sequence using one of the alignment programs described herein using standard parameters. One of skill in the art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning, and the like.
To determine the percent identity of two amino acid sequences or of two nucleic acids, the sequences are aligned for optimal comparison purposes. The percent identity between the two sequences is a function of the number of identical positions shared by the sequences (i.e., percent identity=number of identical positions/total number of positions (e.g., overlapping positions)×100). In one embodiment, the two sequences are the same length. The percent identity between two sequences can be determined using techniques similar to those described below, with or without allowing gaps. In calculating percent identity, typically exact matches are counted.
The determination of percent identity between two sequences can be accomplished using a mathematical algorithm. A nonlimiting example of a mathematical algorithm utilized for the comparison of two sequences is the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87:2264, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-5877. Such an algorithm is incorporated into the BLASTN and BLASTX programs of Altschul et al. (1990) J. Mol. Biol. 215:403. BLAST nucleotide searches can be performed with the BLASTN program, score=100, wordlength=12, to obtain nucleotide sequences homologous to nitrogen-modulated nucleic acid molecules of the invention. BLAST protein searches can be performed with the BLASTX program, score=50, wordlength=3, to obtain amino acid sequences homologous to nitrogen-modulated protein molecules of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (1997) Nucleic Acids Res. 25:3389. Alternatively, PSI-Blast can be used to perform an iterated search that detects distant relationships between molecules. See Altschul et al. (1997) supra. When utilizing BLAST, Gapped BLAST, and PSI-Blast programs, the default parameters of the respective programs (e.g., BLASTX and BLASTN) can be used. See www.ncbi.nlm.nih.gov. Another non-limiting example of a mathematical algorithm utilized for the comparison of sequences is the ClustalW algorithm (Higgins et al. (1994) Nucleic Acids Res. 22:4673-4680). ClustalW compares sequences and aligns the entirety of the amino acid or DNA sequence, and thus can provide data about the sequence conservation of the entire amino acid sequence. The ClustalW algorithm is used in several commercially available DNA/amino acid analysis software packages, such as the ALIGNX module of the Vector NTI Program Suite (Invitrogen Corporation, Carlsbad, Calif.). After alignment of amino acid sequences with ClustalW, the percent amino acid identity can be assessed. A non-limiting example of a software program useful for analysis of ClustalW alignments is GENEDOC™. GENEDOC™ (Karl Nicholas) allows assessment of amino acid (or DNA) similarity and identity between multiple proteins. Another non-limiting example of a mathematical algorithm utilized for the comparison of sequences is the algorithm of Myers and Miller (1988) CABIOS 4:11-17. Such an algorithm is incorporated into the ALIGN program (version 2.0), which is part of the GCG sequence alignment software package (available from Accelrys, Inc., 9865 Scranton Rd., San Diego, Calif., USA). When utilizing the ALIGN program for comparing amino acid sequences, a PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4 can be used.
A preferred program is GAP version 10, which used the algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443-453. GAP Version 10 may be used with the following parameters: % identity and % similarity for a nucleotide sequence using GAP Weight of 50 and Length Weight of 3, and the nwsgapdna.cmp scoring matrix; % identity and % similarity for an amino acid sequence using GAP Weight of 8 and Length Weight of 2, and the BLOSUM62 Scoring Matrix. Equivalent programs may also be used. By “equivalent program” is intended any sequence comparison program that, for any two sequences in question, generates an alignment having identical nucleotide or amino acid residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.
The skilled artisan will further appreciate that changes can be introduced by mutation into the nucleotide sequences of the invention thereby leading to changes in the amino acid sequence of the encoded nitrogen-modulated protein, without altering the biological activity of the protein. Thus, variant isolated nucleic acid molecules can be created by introducing one or more nucleotide substitutions, additions, or deletions into the corresponding nucleotide sequence disclosed herein, such that one or more amino acid substitutions, additions or deletions are introduced into the encoded protein. Mutations can be introduced by standard techniques, such as site-directed mutagenesis and PCR-mediated mutagenesis. Such variant nucleotide sequences are also encompassed by the present invention.
For example, conservative amino acid substitutions may be made at one or more predicted, preferably nonessential amino acid residues. A “nonessential” amino acid residue is a residue that can be altered from the wild-type sequence of a nitrogen-modulated protein without altering the biological activity, whereas an “essential” amino acid residue is required for biological activity. A “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Amino acid substitutions may be made in nonconserved regions that retain function. In general, such substitutions would not be made for conserved amino acid residues, or for amino acid residues residing within a conserved motif, where such residues are essential for protein activity. However, one of skill in the art would understand that functional variants may have minor conserved or nonconserved alterations in the conserved residues. Examples of residues that are conserved and that may be essential for protein activity include, for example, residues that are identical between all proteins contained in an alignment of similar or related sequences known to be involved in nitrogen assimilation. Examples of residues that are conserved but that may allow conservative amino acid substitutions and still retain activity include, for example, residues that have only conservative substitutions between all proteins contained in an alignment of similar or related sequences known to be involved in nitrogen assimilation.
Alternatively, variant nucleotide sequences can be made by introducing mutations randomly along all or part of the coding sequence, such as by saturation mutagenesis, and the resultant mutants can be screened for ability to confer nitrogen utilization efficiency to identify mutants that retain activity. Following mutagenesis, the encoded protein can be expressed recombinantly, and the activity of the protein can be determined using standard assay techniques.
Using methods such as PCR, hybridization, and the like, corresponding nitrogen-modulated sequences can be identified, such sequences having substantial identity to the sequences of the invention. See, for example, Sambrook J., and Russell, D. W. (2001) Molecular Cloning: A Laboratory Manual. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.) and Innis, et al. (1990) PCR Protocols: A Guide to Methods and Applications (Academic Press, NY). In a hybridization method, all or part of the nitrogen-modulated nucleotide sequence can be used to screen cDNA or genomic libraries. Methods for construction of such cDNA and genomic libraries are generally known in the art and are disclosed in Sambrook and Russell, 2001, supra.
Variants and fragments of the nucleotide or amino acid sequences of the present invention generally will encode protein fragments that retain the biological activity of the full-length nitrogen-modulated protein; i.e., retain nitrogen utilization efficiency. By “retains nitrogen utilization efficiency” is intended that the variant or fragment will have at least about 30%, at least about 50%, at least about 70%, or at least about 80% of the nitrogen utilization efficiency of the full-length nitrogen-modulated protein disclosed herein as SEQ ID NO: 3, 5, 8, 10, 12, 14, 16, 18, 23, 25, 27, 29, 31, 33, 35, 37, or 39, or the full-length nitrogen-modulated nucleotide sequence disclosed herein as SEQ ID NO: 2, 4, 7, 9, 11, 13, 15, 17, 22, 24, 26, 28, 30, 32, 34, 36, or 38. Methods for monitoring nitrogen utilization efficiency include detecting a change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (for example, a measurable change in nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content) or detecting the ability of a plant to provide the same or elevated yield at lower nitrogen fertilization levels, or the ability of a plant to provide elevated yields at the same nitrogen fertilization levels when compared to a plant that does not contain or express a nitrogen-modulated sequence of the invention.
The polypeptide sequences useful in the present invention may be altered in various ways including amino acid substitutions, deletions, truncations, and insertions. Methods for such manipulations are generally known in the art. For example, amino acid sequence variants of the nitrogen-modulated proteins disclosed herein can be prepared by mutations in the nucleotide sequences. This may also be accomplished by one of several forms of mutagenesis and/or in directed evolution. In some aspects, the changes encoded in the amino acid sequence will not substantially affect function of the protein. Such variants will possess the desired nitrogen utilization efficiency. However, it is understood that the ability of the nitrogen-modulated sequences of the invention to alter or improve nitrogen utilization may be further improved by one use of such techniques upon the compositions of this invention. For example, one may express the nucleotide sequences disclosed herein in host cells that exhibit high rates of base misincorporation during DNA replication, such as XL-1 Red (Stratagene, La Jolla, Calif.). After propagation in such strains, one can isolate the DNA (for example by preparing plasmid DNA, or by amplifying by PCR and cloning the resulting PCR fragment into a vector), transform it into plants as described elsewhere herein, and measure nitrogen utilization efficiency.
Alternatively, alterations may be made to the protein sequence of many proteins at the amino or carboxy terminus without substantially affecting activity. This can include insertions, deletions, or alterations introduced by modern molecular methods, such as PCR, including PCR amplifications that alter or extend the protein coding sequence by virtue of inclusion of amino acid encoding sequences in the oligonucleotides utilized in the PCR amplification. Alternatively, the protein sequences added can include entire protein-coding sequences, such as those used commonly in the art to generate protein fusions. Such fusion proteins are often used to (1) increase expression of a protein of interest, (2) introduce a binding domain, enzymatic activity, or epitope to facilitate either protein purification, protein detection, or other experimental uses known in the art, or, (3) target secretion or translation of a protein to a subcellular organelle, such as the periplasmic space of gram-negative bacteria, or the endoplasmic reticulum of eukaryotic cells, the latter of which often results in glycosylation of the protein.
Variant nucleotide and amino acid sequences of the present invention also encompass sequences derived from mutagenic and recombinogenic procedures such as DNA shuffling. With such a procedure, one or more different nitrogen-modulated protein coding regions can be used to create a new nitrogen-modulated protein possessing the desired properties. In this manner, libraries of recombinant polynucleotides are generated from a population of related sequence polynucleotides comprising sequence regions that have substantial sequence identity and can be homologously recombined in vitro or in vivo. For example, using this approach, sequence motifs encoding a domain of interest may be shuffled between the nitrogen-modulated sequence useful in the present invention and other known nitrogen-modulated sequences to obtain a new sequence coding for a protein with an improved property of interest, such as improved nitrogen utilization. Strategies for such DNA shuffling are known in the art. See, for example, Stemmer (1994) Proc. Natl. Acad. Sci. USA 91:10747-10751; Stemmer (1994) Nature 370:389-391; Crameri et al. (1997) Nature Biotech. 15:436-438; Moore et al. (1997) J. Mol. Biol. 272:336-347; Zhang et al. (1997) Proc. Natl. Acad. Sci. USA 94:4504-4509; Crameri et al. (1998) Nature 391:288-291; and U.S. Pat. Nos. 5,605,793 and 5,837,458.
Plant Transformation
Methods of the invention involve introducing a nucleotide construct into a plant. By “introducing” is intended to present to the plant the nucleotide construct in such a manner that the construct gains access to the interior of a cell of the plant. The methods of the invention do not require that a particular method for introducing a nucleotide construct to a plant is used, only that the nucleotide construct gains access to the interior of at least one cell of the plant. Methods for introducing nucleotide constructs into plants are known in the art including, but not limited to, stable transformation methods, transient transformation methods, and virus-mediated methods.
In general, plant transformation methods involve transferring heterologous DNA into target plant cells (e.g. immature or mature embryos, suspension cultures, undifferentiated callus, protoplasts, etc.), followed by applying a maximum threshold level of appropriate selection (depending on the selectable marker gene) to recover the transformed plant cells from a group of untransformed cell mass. Explants are typically transferred to a fresh supply of the same medium and cultured routinely. Subsequently, the transformed cells are differentiated into shoots after placing on regeneration medium supplemented with a maximum threshold level of selecting agent (i.e., antibiotics, such as spectinomycin and kanamycin). The shoots are then transferred to a selective rooting medium for recovering rooted shoot or plantlet. The transgenic plantlet then grow into mature plant and produce fertile seeds (e.g. Hiei et al. (1994) The Plant Journal 6:271-282; Ishida et al. (1996) Nature Biotechnology 14:745-750). Explants are typically transferred to a fresh supply of the same medium and cultured routinely. A general description of the techniques and methods for generating transgenic plants are found in Ayres and Park (1994) Critical Reviews in Plant Science 13:219-239 and Bommineni and Jauhar (1997) Maydica 42:107-120. Since the transformed material contains many cells, both transformed and non-transformed cells are present in any piece of subjected target callus or tissue or group of cells. The ability to kill non-transformed cells and allow transformed cells to proliferate results in transformed plant cultures. Often, the ability to remove non-transformed cells is a limitation to rapid recovery of transformed plant cells and successful generation of transgenic plants. Molecular and biochemical methods can then be used to confirm the presence of the integrated heterologous gene of interest in the genome of transgenic plant.
Generation of transgenic plants may be performed by one of several methods, including but not limited to introduction of heterologous DNA by Agrobacterium into plant cells (Agrobacterium-mediated transformation), bombardment of plant cells with heterologous foreign DNA adhered to particles, and various other non-particle direct-mediated methods (e.g. Hiei et al. (1994) The Plant Journal 6:271-282; Ishida et al. (1996) Nature Biotechnology 14:745-750; Ayres and Park (1994) Critical Reviews in Plant Science 13:219-239; Bommineni and Jauhar (1997) Maydica 42:107-120) to transfer DNA.
Methods for transformation of chloroplasts are known in the art. See, for example, Svab et al. (1990) Proc. Natl. Acad. Sci. USA 87:8526-8530; Svab and Maliga (1993) Proc. Natl. Acad. Sci. USA 90:913-917; Svab and Maliga (1993) EMBO J. 12:601-606. The method relies on particle gun delivery of DNA containing a selectable marker and targeting of the DNA to the plastid genome through homologous recombination. Additionally, plastid transformation can be accomplished by transactivation of a silent plastid-borne transgene by tissue-preferred expression of a nuclear-encoded and plastid-directed RNA polymerase. Such a system has been reported in McBride et al. (1994) Proc. Natl. Acad. Sci. USA 91:7301-7305.
Transformation of bacterial cells is accomplished by one of several techniques known in the art, including but not limited to electroporation or chemical transformation (see, for example, Ausubel, ed. (1994) Current Protocols in Molecular Biology, John Wiley and Sons, Inc., Indianapolis, Ind.). Markers conferring resistance to toxic substances are useful in identifying transformed cells (having taken up and expressed the test DNA) from non-transformed cells (those not containing or not expressing the test DNA).
In one aspect of the invention, the nucleotide sequences of the invention are useful as markers to assess transformation of bacterial or plant cells. In this manner, transformation is assessed by monitoring nitrogen utilization efficiency as described above.
Transformation of plant cells can be accomplished in similar fashion. By “plant” is intended whole plants, or component parts including plant organs (e.g., leaves, stems, roots, etc.), seeds, plant cells, propagules, embryos and progeny of the same. Plant cells can be differentiated or undifferentiated (e.g. callus, suspension culture cells, protoplasts, leaf cells, root cells, phloem cells, pollen). “Transgenic plants” or “transformed plants” or “stably transformed” plants or cells or tissues refer to plants that have incorporated or integrated exogenous nucleic acid sequences or DNA fragments into the plant cell. By “stable transformation” is intended that the nucleotide construct introduced into a plant integrates into the genome of the plant and is capable of being inherited by progeny thereof.
The cells that have been transformed may be grown into plants in accordance with conventional ways. See, for example, McCormick et al. (1986) Plant Cell Reports 5:81-84. These plants may then be grown, and either pollinated with the same transformed strain or different strains, and the resulting hybrid having constitutive expression of the desired phenotypic characteristic identified. Two or more generations may be grown to ensure that expression of the desired phenotypic characteristic is stably maintained and inherited and then seeds harvested to ensure expression of the desired phenotypic characteristic has been achieved. In this manner, the present invention provides transformed seed (also referred to as “transgenic seed”) having a nucleotide construct of the invention, for example, an expression cassette of the invention, stably incorporated into their genome.
Methods to Increase Plant Yield by Modulating Nitrogen Utilization
Methods for increasing plant yield are provided. The methods comprise introducing into a plant or plant cell a nitrogen-modulated nucleotide sequence disclosed herein such that an increase in nitrogen utilization efficiency corresponds to an increase in plant yield. As defined herein, the “yield” of the plant refers to the quality and/or quantity of biomass produced by the plant. By “biomass” is intended any measured plant product. An increase in biomass production is any improvement in the yield of the measured plant product. Increasing plant yield has several commercial applications. For example, increasing plant leaf biomass may increase the yield of leafy vegetables for human or animal consumption. Additionally, increasing leaf biomass can be used to increase production of plant-derived pharmaceutical or industrial products. An increase in yield can comprise any statistically significant increase including, but not limited to, at least a 1% increase, at least a 3% increase, at least a 5% increase, at least a 10% increase, at least a 20% increase, at least a 30%, at least a 50%, at least a 70%, at least a 100% or a greater increase.
Plants
The present invention may be used for transformation of any plant species, including, but not limited to, monocots and dicots. Examples of plants of interest include, but are not limited to, corn (maize), sorghum, wheat, sunflower, tomato, crucifers, peppers, potato, cotton, rice, soybean, sugarbeet, sugarcane, tobacco, barley, and oilseed rape, Brassica sp., alfalfa, rye, millet, safflower, peanuts, sweet potato, cassaya, coffee, coconut, pineapple, citrus trees, cocoa, tea, banana, avocado, fig, guava, mango, olive, papaya, cashew, macadamia, almond, oats, vegetables, grasses (such as turf grasses, forage grasses, or pasture grasses), ornamentals, fruit trees, and conifers.
Vegetables include, but are not limited to, onions, tomatoes, lettuce, green beans, lima beans, peas, and members of the genus Curcumis such as cucumber, cantaloupe, and muskmelon. Ornamentals include, but are not limited to, azalea, hydrangea, hibiscus, roses, tulips, daffodils, petunias, carnation, poinsettia, and chrysanthemum. Preferably, plants of the present invention are crop plants (for example, maize, sorghum, wheat, sunflower, tomato, crucifers, peppers, potato, cotton, rice, soybean, sugarbeet, sugarcane, tobacco, barley, oilseed rape, etc.).
This invention is particularly suitable for any member of the monocot plant family including, but not limited to, maize, rice, barley, oats, wheat, sorghum, rye, sugarcane, pineapple, yams, onion, banana, coconut, and dates.
Evaluation of Plant Transformation
Following introduction of heterologous foreign DNA into plant cells, the transformation or integration of heterologous gene in the plant genome is confirmed by various methods such as analysis of nucleic acids, proteins and metabolites associated with the integrated gene.
PCR analysis is a rapid method to screen transformed cells, tissue or shoots for the presence of incorporated nucleotide sequences at the earlier stage before transplanting into the soil (Sambrook and Russell (2001) Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.). PCR is carried out using oligonucleotide primers specific to the gene of interest or Agrobacterium vector background, etc.
Plant transformation may be confirmed by Southern blot analysis of genomic DNA (Sambrook and Russell, 2001, supra). In general, total DNA is extracted from the transformant, digested with appropriate restriction enzymes, fractionated in an agarose gel and transferred to a nitrocellulose or nylon membrane. The membrane or “blot” is then probed with, for example, radiolabeled ³²P target DNA fragments to confirm the integration of the introduced gene in the plant genome according to standard techniques (Sambrook and Russell, 2001, supra).
In Northern analysis, RNA is isolated from specific tissues of transformant, fractionated in a formaldehyde agarose gel, blotted onto a nylon filter according to standard procedures that are routinely used in the art (Sambrook and Russell, 2001, supra). Expression of RNA encoded by the nucleotide sequence of the invention is then tested by hybridizing the filter to a radioactive probe derived from a polynucleotide of the invention, by methods known in the art (Sambrook and Russell, 2001, supra)
Western blot and biochemical assays and the like may be carried out on the transgenic plants to determine the presence of protein encoded by the nitrogen-modulated gene by standard procedures (Sambrook and Russell, 2001, supra) using antibodies that bind to one or more epitopes present on the nitrogen-modulated protein. For example, the polyclonal antibodies generated by the methods of the present invention can be used to detect the presence of a nitrogen-modulated protein.
Antibodies
Antibodies to the polypeptides useful in the present invention, or to variants or fragments thereof, are also encompassed. Methods for producing antibodies are well known in the art (see, for example, Harlow and Lane (1988) Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.; U.S. Pat. No. 4,196,265).

EXPERIMENTAL

Materials and Methods

The majority of the starting genetic material for this project was provided in the form of maize expressed sequence tags, or “ESTs”, derived from a microarray experiment to identify potential genes up- or down-regulated in response to nitrogen. The microarray experiment identified several hundred possible candidates for possible use in transformations. While these sequences were predictive of gene transcription as a response to nitrogen fluctuations, they did not provide a firm identification of genes that were regulated in response to nitrogen levels or genes that regulate nitrogen levels. The candidate ESTs from the microarray experiment were screened based on genomic selection criteria to analyze and determine a small number of priority candidates for subsequent use in transgenic expression as described in this specification. All EST sequences that were entered into the project (i.e., “project genes”) were first examined to identify open reading frames that could encode a protein that was responsive to plant nitrogen levels. Multiple open reading frames were typically present within an EST. Ultimately, individual project genes were selected based on multiple criteria, including size of open reading frame wherein longer open reading frames were preferentially selected, and predicted function of translated genes, wherein individual open reading frames were translated and then subjected to a BLAST search to identify protein homologues. In cases where homologues were identified, we inferred that the gene was likely to encode a protein with a similar function. This information was used to assess if genes might encode protein functions with relevance to nitrogen assimilation in plants.
By this selection process, an individual gene target was selected from each EST. The complete gene sequence selected from each EST is disclosed in the following examples. One of the EST sequences (N-EST 77-A01) was used as a source for two different genes that were entered into the project (N-EST77A and N-EST77B) and for one other EST (EST N-EST76-H12). We discovered that the EST could be modified to generate an open reading frame that is longer than the reading frames present in the unmodified EST. In summary, three open reading frames were combined to create one longer gene (“N-EST76A”).
In some cases, a DNA sample provided from the microarray experiment was used as the source material for all subsequent DNA cloning steps. In cases where the EST sample was not suitable, synthetic sequences were generated. The N-EST76b gene was ordered as a synthetic gene from the vendor Blue Heron Biotechnology, Inc. (Bothell, Wash.). The gene sequence for each EST and each synthetic gene was confirmed by DNA sequencing prior to subcloning each gene for protein overexpression.
Protein Overexpression and Purification
Each of the genes selected for the project were subcloned into an expression vector that facilitates protein overexpression in E. coli. The protein overexpression was carried out to allow individual proteins to be purified. The purified proteins can be used to generate polyclonal antibodies against each protein in a pair of rabbits. Finally, the polyclonal antibodies can be used to detect the presence of target proteins in transgenic plants.
Using methods known in the art, each of the project genes was subcloned into the E. coli expression vector pRSF1b (Invitrogen Corporation, Carlsbad, Calif.). Resulting clones were confirmed by DNA sequencing, and used to induce expression of each protein in E. coli. The expressed His-tagged protein was then purified as known in the art using a cobalt affinity resin (Clontech Laboratories, Inc., Mountain View, Calif.).
Plant Transformation
Representative project genes were subcloned into vectors to carry out Agrobacterium-mediated transformation of maize. Following vector construction and transformation of Agrobacterium, the vectors were confirmed by Southern blot by methods known in the art. Positive Agrobacterium strains that passed these tests were then grown on a solid medium to produce cell counts for large-scale transformation experiments.
The following examples describe the methods for plant vector construction and plant transformation.
Vector Construction for Plant Transformation
The open reading frame (ORF) for each project gene is amplified by PCR from the maize EST sequence or synthetic gene. Restriction sites (BamH I and Asc I, for example) are added to each end of the ORF during PCR. Additionally, the nucleotide sequence ACC is added immediately 5′ to the start codon of the gene to increase translational efficiency (Kozak (1987) Nucleic Acids Research 15:8125-8148; Joshi (1987) Nucleic Acids Research 15:6643-6653). The PCR product is subcloned into an intermediate vector (for example, pRSF-1b) and sequenced, using techniques well known in the art, to ensure that no mutations are introduced during PCR. The plasmid containing the project gene is digested with, for example, BamH I and Pst I and a fragment containing the intact ORF is isolated and purified.
The purified DNA fragment containing the project ORF is then subcloned into a plasmid such as pSB11 (Japan Tobacco, Inc.), for example at a BamH I and Pst I site, to complete the plant expression vector. The plant expression vector contains, for example, a Tripsacum ubiquitin promoter, TripPro5 promoter (U.S. patent application Ser. No. 11/377,318 filed Mar. 16, 2006, incorporated herein by this reference) and the PinIl terminator (An et al. (1989) The Plant Cell 1:115-122) to form the final plasmid, referred to herein as pSB11-1A. pSB11-IA is organized such that the DNA fragment containing, for example, the promoter—NUE gene—terminator construct may be excised by appropriate restriction enzymes and also used for transformation into plants, for example, by aerosol beam injection. The structure of pSB11-1A is verified by restriction digest and gel electrophoresis, as well as by sequencing across the various cloning junctions.
The plasmid is mobilized into Agrobacterium tumefaciens strain LBA4404 which also harbors the plasmid pSB 1 (Japan Tobacco, Inc.), using triparental mating procedures well known in the art, and plated on media containing antibiotic. Plasmid pSB11-1A carries spectinomycin resistance but is a narrow host range plasmid and cannot replicate in Agrobacterium. Antibiotic resistant colonies arise when pSB11-1A integrates into the broad host range plasmid pSB1 through homologous recombination. The resulting cointegrate product is verified by Southern hybridization. The Agrobacterium strain harboring the cointegrate can be used to transform plants, for example, by the PureIntro method (Japan Tobacco, Inc.).
Transformation of Plant Cells by Agrobacterium-Mediated Transformation
Ears are collected 8-12 days after pollination. Embryos are isolated from the ears, and those embryos 0.8-1.5 mm in size are used for transformation. Embryos are plated scutellum side-up on a suitable incubation media, and incubated overnight at 25° C. in the dark. However, it is not necessary per se to incubate the embryos overnight. Embryos are contacted with an Agrobacterium strain containing the appropriate vectors for Ti plasmid mediated transfer for 5-10 min, and then plated onto co-cultivation media for 3 days (25° C. in the dark). After co-cultivation, explants are transferred to recovery period media for five days (at 25° C. in the dark). Explants are incubated in selection media for up to eight weeks, depending on the nature and characteristics of the particular selection utilized. After the selection period, the resulting callus is transferred to embryo maturation media, until the formation of mature somatic embryos is observed. The resulting mature somatic embryos are then placed under low light, and the process of regeneration is initiated as known in the art. The resulting shoots are allowed to root on rooting media, and the resulting plants are transferred to nursery pots and propagated as transgenic plants. At this time, leaf samples are isolated and the presence of the gene of interest is confirmed by PCR.
All plants generated in this manner were grown to seed set and crossed with pollen isolated from with Hi-II plants (Iowa State University, Ames, Iowa). The fertilized plants were grown until maturity. Mature seeds were harvested from individual plants and saved for future testing in the T1 generation, if necessary.
Protein Expression in Transgenic Plants
Protein expression in representative transgenic maize events was estimated by Western blot. Briefly, leaf samples were taken after 4 weeks of growth in the greenhouse and immediately frozen on dry ice. Total protein was extracted (P-PER plant protein extraction kit, Pierce) and the protein concentration determined by Bradford assay. Individual plant protein samples were separated by electrophoresis, transferred to nitrocellulose, and the immobilized proteins were contacted with rabbit polyclonal antiserum using methods known in the art. Bound antibody complexes were visualized with the ECL Plus Western Blotting detection system (GE Healthcare Bio-Sciences Corp., Piscataway, N.J.).
Nitrogen Assay Methods
In preparation for nitrogen assays, leaves were sliced from plants two or four weeks after transfer from tissue culture to the greenhouse (or four weeks from germination for T1 plants). The material was snap frozen on dry ice and stored at −80° C. prior to processing.
Nitrate
Fifty milligrams of leaf material (fresh weight, no midrib) were freeze-dried for dry weight determination. The dehydrated leaf tissue was then ground in the presence of fresh Milli Q water using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 0.45 μm Polyvinylidene Fluoride (PVDF) filter and injected into an Agilent 1100 HPLC running a mobile phase of a mixture of 1.8 mM sodium carbonate and 1.7 mM sodium bicarbonate at 1.5 ml/min. Ions were separated using an IonPac AS9-SC ion chromatography column equipped with a guard column. Analysis was performed using anion auto-suppressed conductivity with a self-regenerating suppressor operating in recycle mode. Samples were compared to internal standards included in each sample run.
Ammonium
Fifty milligrams of leaf material (fresh weight, no midrib) were ground in the presence of 60% methanol using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 0.45 μm Polyvinylidene Fluoride (PVDF) filter and injected into an Agilent 1100 HPLC equipped with a 3.3 m, 63° C. stainless steel coil and cooled autosampler. The mobile phase contained 3 mM o-phthalaldehyde (OPA), 10 mM β-mercaptoethanol, and 100 mM phosphate buffer (pH6.8) running at 0.4 ml/min. Fluorescence (excitation 410 nm and emission 470 nm) and diode array detection (410 nm) were used for the quantification of ammonium in the leaf extracts. Internal ammonium standards were included in each run for comparison.
Amino Acids by HPLC
Fifty milligrams of leaf material (fresh weight, no midrib) were freeze-dried for dry weight determination. The dehydrated leaf tissue was then ground in the presence of fresh Milli Q water using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 0.45 μm Polyvinylidene Fluoride (PVDF) filter and injected into an Agilent 1100 HPLC using a Zorbax Eclipse AAA, 4.6×75 mm reverse phase column equipped with a guard column. A cooled autosampler was used to mix the leaf extract with 400 mM borate buffer (pH 10.2), 1% o-phthalaldehyde/1% 3-mercaptopropionic acid in methanol, which was then diluted with water prior to injection. The details of the injector program are as follows: 0.5 μl sample are added to 2.5 μl borate buffer and mixed at maximum speed two times. After a 0.5 minute hold, the needle is placed in water to remove residue from the tip and then 0.5 μl OPA solution is added. The combined 3.5 μl is mixed at maximum speed six times. The needle is again placed in water to rinse the tip and then placed into a vial containing fresh water. Next, 32 μl Milli Q water are added to the sample mixture, and 18 μl are mixed at maximum speed two times. The sample solution is then injected into the HPLC with the pump running a 2 ml/min mobile phase of 40 mM Na2HPO4 (pH 7.8) (A) with a gradient from 0 to 26% acetonitrile/methanol/water (45:45:10) (B) in five minutes followed by a 100% hold B for two minutes then 100% A for two minutes. Quantification of asparagine, glutamine, glutamic acid, and aspartic acid was performed by diode array detection (328 to 348 nm) and fluorescence detection (excitation 340 nm, emission 450 nm). Samples were compared to asparagine, glutamine, glutamic acid, and aspartic acid internal standards included in each sample run.
Total Amino Acids
Fifty milligrams of leaf material (fresh weight, no midrib) were freeze-dried for dry weight determination. The dehydrated leaf tissue was then ground in the presence of fresh Milli Q water using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 0.45 μm Polyvinylidene Fluoride (PVDF) filter. Dilutions of leaf extract were performed in water, and ninhydrin reagent solution (ninhydrin and hydrindantin in DMSO and lithium acetate buffer, pH 5.2) was added. The samples were then sealed with a thick foil tape, heated for ten minutes at 90° C., cooled for exactly two minutes, and read in a spectrophotometer at 590 nm. Values were compared with internal standards included during each sample analysis.
Total Protein
Fifty milligrams of leaf material (fresh weight, no midrib) were freeze-dried for dry weight determination. The dehydrated leaf tissue was then ground in the presence of fresh Milli Q water using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 0.45 μm Polyvinylidene Fluoride (PVDF) filter. Bio-Rad Protein Dye was added to leaf samples diluted in water, and a Bradford protein assay was performed and read in the spectrophotometer at 595 nm vs. internal protein standards included in the assay.
Chlorophyll
Fifty milligrams of leaf material (fresh weight, no midrib) were ground in the presence of 60% methanol using a MiniBeadbeater-96™ and 2.3 mm stainless-steel beads. The ground leaf tissue was filtered through a 1.0 μm A/B glass fiber filter, and 100 μl extract was placed in a Corning 3370 flat bottom microplate and read in spectrophotometer with wells blanked with an equivalent volume of 60% methanol. SoftMax Pro software was used to convert the light pathlength to 1 cm. Calculations of chlorophyll content were performed using equations from Porra, R. J. Photosynthesis Research, 73: 149-156, 2002.

Example 1

Identification of Candidate ESTs

The nucleotide sequence information for each of the candidate nitrogen-modulated genes was generated in a differential nitrogen microarray experiment conducted at the direction of applicant by Dr. Pat Schnable at Iowa State University. This microarray experiment was used as an initial screen to select a sub-set of ESTs that may be related to nitrogen conditions.
From the large number of EST sequences showing some difference in the microarray (136 with both 3′ and 5′ data), further selections were made following a bioinformatics analysis. This analysis included checking for nucleotide sequence similarities in the International Nucleotide Sequence Database (housed at NCBI), checking for predicted protein similarities in the protein databases, such as NCBI and Swisspro, exploring information concerning known or predicted function, and checking the nucleotide and protein databases at the patent office. Using the results of these analyses, as well as supporting key information, a subset of ESTs was selected for transgenic overexpression in corn in relation to nitrogen use efficiency. For each of the EST sequences, an open reading frame was identified and translated into an amino acid sequence. A list of the candidate nitrogen-modulated sequences is provided in Table 1.
Vector Construction for Overexpression of Nitrogen-Modulated Sequences in Plants
An open reading frame for each of the candidate nitrogen-modulated ESTs and subsequently introduced into vectors for plant expression. Using an approach well-known in the art, two different selectable marker systems which allow selection of transformed plants in the presence of a selection agent were employed.
Maize Transformation with Nitrogen-Modulated Genes
The plant vectors described are useful for plant transformation experiments to introduce the nitrogen-modulated genes into the maize genome using the methods described above.

TABLE 1

Nitrogen-modulated sequences

	EST	Open reading	Protein
	Sequence	frame	sequence
	(SEQ ID	(SEQ ID	(SEQ ID	pAX
EST Name	NO:)	NO:)	NO:)	number

N-EST213	1	2	3	pAX2411
				pAX2410
N-EST45-C08		4	5	pAX3404
N-EST77-A¹	6	7	8	pAX3405
N-EST77-B¹	6	9	10	pAX3406
N-EST61-A10		11	12	pAX2422
N-EST88-H03		13	14	pAX2425
N-EST15		15	16	pAX2437
N-EST42-B12		17	18	pAX2435
N-EST76a²	19	22	23	pAX2433
N-EST76b²	19	24	25	pAX2431
N-EST31-A10		26	27	pAX2441
N-EST43		28	29	pAX2443
N-EST264		30	31	pAX2437
N-EST28		32	33	pAX2439
N-EST13A-A08		34	35	pAX2454
N-EST13E-E07		36	37	pAX2457
N-EST55C-C10		38	39	pAX2460

¹See Example 2
²See Example 3

Example 2

Two Maize Proteins N-EST 77A, N-EST 77B

This invention describes the use of a maize gene sequences (from EST N-EST77-A01) to confer enhanced nitrogen utilization in transgenic maize (Zea mays). Two open reading frames are joined to a highly active plant promoter and a terminus to express each protein following integration into the maize genome. The ectopically expressed proteins will enhance the maize plant's ability to utilize available nitrogen.
Bioinformatics analysis revealed that there was no significant sequence homology with other sequences in the NCBI database. One portion showed some homology to a CCAAT-binding transcription factor in other species but not in maize. When the nucleotide sequence was received from the microarray experiment, there was also a predicted protein sequence. The predicted protein is referred to herein as N-EST77A. Examination of the nucleotide sequence indicated that the nucleotide could code for another protein (subsequently confirmed), and that protein sequence is referred to as N-EST77B. This second protein was not predicted in any information received from the microarray experiment.
For expression of N-EST 77B, the first amino acid was changed from a leucine to a methionine to improve protein expression.

Example 3

Maize Protein N-EST76

This Example describes the use of a maize gene sequence (from EST N-EST76-H12) to confer enhanced nitrogen utilization in transgenic maize (Zea mays). This particular EST possesses part of the nucleotide sequence that is homologous to the so-called “bZIP” class of transcription factors. For this invention, two separate gene constructs are overexpressed in plants. One construct (“N-EST76a”) contains the modified version of the N-EST76-H12 EST to allow a longer open reading frame to be expressed in maize. This modified gene contains 3 substitutions when compared to the gene sequence in the native EST. A second gene is also created which adds a basic region leucine zipper sequence to the 3′ end of the gene. The resulting gene is referred to as “N-EST76b”
The full-length clone sequence appeared to contain two different regions that code for proteins, protein I of 108 amino acids and protein II of 122 amino acids. It was recognized, however, that if the full-length clone had not been sequenced accurately and a mistake had been made in the sequencing in the middle of the clone, a frameshift may have artificially generated a new start codon when it should not be there, thus suggesting two regions when there is only one longer region. To accommodate this possibility, the sequence analysis was done assuming that both the two shorter regions and the one longer region existed. Briefly, the nucleotide sequence searches returned results that indicated that the “I” sequence had some homology with a hypothetical protein from rice (genomic DNA from the rice genome program), and minor homology with some putative bZIP TFs. The nucleotide patent database search showed that sequence I had some homology (E=2e-06) with sequences that were noted to be transcription factors (e.g. WO03007699). A predicted amino acid sequence for 1 from the microarray assay was used to search against the databases and no significant hits were found. However, when the nucleotide sequence I was re-translated using GenBank tools, or the ExPasy tool, the predicted protein sequences were found to have: (1) Hits against the GenBank protein dbase (e.g. E=9e-09) with suggested function being a bZIP transcription factor; and (2) hits against the patent protein database (e.g. E=7e-05) with function being associated with a bZIP transcription factor (especially from rice), or an ABA-responsive element-binding protein (mostly from Arabidopsis, e.g. U.S. Pat. No. 6,245,905).
Confirmation of DNA Sequence
The DNA construct that contained N-EST76-H12 was sequenced to confirm the sequence provided from the microarray assay. This sequencing effort revealed a single nucleotide substitution at position 1121 of SEQ ID NO: 19, in which a “G” is present in place of a “C”. This substitution is located in an open reading frame described for N-EST76, and leads to the substitution of a glutamine for a glutamic acid in the protein sequence. The correct DNA sequence for the full N-EST76-H12 EST is represented in SEQ ID NO: 19.
Cloning Strategy to Generate N-EST76a and N-EST76b
The DNA sequence in N-EST76-H12 contains 3 open reading frames that are separated by two stop codons and one frameshift. The cloning strategy employed was to eliminate both stop codons and the frameshift to produce a continuous open reading frame that is more similar to known bZIP proteins and is thus more likely to function properly when expressed. Additionally, bZIP proteins typically contain a basic region leucine zipper at the C-terminal end of the protein. N-EST76-H12 does not contain such a domain. Thus, a second protein was created which adds a basic region leucine zipper domain to the end of the N-EST76 protein.
Elimination of Stop Codons and Frameshift in N-EST76-H12
For this Example, the maize sequence described in the EST N-EST76-H12 (SEQ ID NO:19) was modified to produce a longer open reading frame that is more homologous to full-length bZIP proteins. This required 3 modifications to the N-EST76 sequence:
Substitution of cytosine in place of thymine at nucleotide position 444
Substitution of guanine in place of adenine at nucleotide position 673
Addition of guanine after nucleotide position 722
The first two substitutions served to remove a pair of stop codons that are present in the N-EST76 EST in reading frame 3. The last change (addition after nucleotide position 722) introduced a frameshift to connect reading frame 3 to reading frame 2 to generate a reading frame that is more homologous to full-length bZIP proteins. The DNA sequence is presented in SEQ ID NO: 22 and the protein that is expressed from the resulting construct is referred to as “N-EST76a” (SEQ ID NO:23).
Addition of Basic Region Leucine Zipper to N-EST76a
Additionally, we create a second gene in which a DNA fragment encoding a basic region leucine zipper was added to the 3′ end of N-EST76a. This zipper domain is lacking in the EST for N-EST76, and is added here to create a N-EST76-derived protein that is more similar to the bZIP proteins described in the literature. Thus, a protein which is identical to N-EST76a is created except that it possesses an added zipper domain at the C-terminus. This new DNA sequence is represented in SEQ ID NO: 24 and the protein is referred to as “N-EST76b” (SEQ ID NO: 25).
These cloning strategies are summarized below.
Selection of bZIP Domain for Project
The selection of a bZIP domain for this project was carried out by selecting proteins with high homology to the translated N-EST76a sequence using the blastx search algorithm. This approach led to the identification of a rice bZIP protein with significant homology to the N-EST76a protein. The protein sequence of this rice bZIP protein (accession number BAD17130) is presented herein as SEQ ID NO: 20, with the bZIP domain represented by amino acid positions 275-357 of SEQ ID NO: 20.
The DNA sequence encoding the complete rice bZIP protein is presented in SEQ ID NO: 21, with the DNA fragment coding for the basic region leucine zipper represented by nucleotide positions 826-1074 of SEQ ID NO:21. This bZIP DNA sequence was optimized for maize codon usage and then added to the 3′ end of the N-EST76a gene sequence (nucleotide position 1130 in N-EST76-H12) to create the N-EST76b gene sequence (SEQ ID NO: 24).

Example 4

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST76a and N-EST76b

As described in a previous Example, the plant transformation vectors pAX2433 and pAX2431 were constructed to direct overexpression of the N-EST76a and N-EST76b proteins in maize.
Each vector was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX2433 or pAX2431 to recombine in vivo to create a vector that can direct insertion of the N-EST76a or N-EST76b cassette into the maize genome. The formation of each recombinant vector (pAG2433, pAG2431) was confirmed by Southern blot hybridization of the Agrobacterium strain.
The Agrobacterium strains containing pAG2433 or pAG2431 were co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Nitrogen Assimilation in Maize Plants Expressing N-EST76a, N-EST76b
Nitrogen Assays, T0 Events
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 24 transgenic plants containing the N-EST76a gene and 6 plants containing the N-EST76b gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. Included alongside in the analysis were plants that were transformed with a construct containing only the selectable marker (no N-EST76a or N-EST76b). These plants were likewise sampled at 4 weeks and are referred to as “non GOT” plants. The results of the nitrogen assays carried out on both types of plants are shown below in Table 2.

TABLE 2

Nitrogen levels, N-EST76a and N-EST76b vs. non GOI maize events, 4 weeks following transfer to soil

								Total		Total
					Aspartic	Glutamic		Amino	Total	Chlorophyll
		Nitrate	Asparagine	Glutamine	Acid	Acid	Ammonium	Acids	protein	(a + b)
Plant #	GOI	(μg/g)	(μg/g)	(μg/g)	(μg/g)	(μg/g)	(μg/g)	(mg/g)	(mg/g)	(mg/g)

6164	N-EST76a	259	181	159	798	2596	112	120	9.18	0.048
6165	N-EST76a	557	288	204	546	3156	179	164	18.43	0.057
6166	N-EST76a	170	132	180	377	2921	122	163	15.97	0.040
6167	N-EST76a	394	346	178	459	2430	122	132	12.70	0.056
6170	N-EST76a	292	113	172	449	2857	126	147	10.09	0.028
6172	N-EST76a	259	160	198	326	2856	130	156	17.13	0.040
6173	N-EST76a	300	211	210	140	2024	179	152	17.52	0.069
6174	N-EST76a	15572	1604	208	470	2287	433	161	17.83	0.143
6175	N-EST76a	448	287	247	574	2542	247	166	15.73	0.078
6176	N-EST76a	272	231	207	306	3146	172	161	14.20	0.049
6178	N-EST76a	380	816	387	503	3152	170	169	6.71	0.044
6287	N-EST76a	772	126	372	290	2821	188	133	9.08	0.050
6288	N-EST76a	418	222	367	214	3010	114	153	10.02	0.036
6289	N-EST76a	153	90	288	109	2529	168	136	8.46	0.073
6290	N-EST76a	388	758	428	490	2584	196	169	9.78	0.074
6291	N-EST76a	241	112	277	697	1905	170	126	7.31	0.082
6292	N-EST76a	186	136	426	561	2259	158	144	14.21	0.066
6293	N-EST76a	628	277	712	491	2582	490	185	10.01	0.070
6294	N-EST76a	470	271	413	744	2794	182	121	10.96	0.073
6295	N-EST76a	197	169	484	263	2395	160	146	19.75	0.063
6296	N-EST76a	291	528	391	314	2537	153	130	13.80	0.046
6297	N-EST76a	173	217	406	358	2886	167	160	15.94	0.132
6298	N-EST76a	383	149	570	684	2277	629	121	8.41	0.046
6299	N-EST76a	524	364	439	191	1723	404	166	13.55	0.061
6155	N-EST76b	426	378	338	564	3587	142	180	14.57	0.045
6156	N-EST76b	114	190	208	987	3209	122	171	12.04	0.041
6158	N-EST76b	1449	690	258	298	2986	127	171	19.55	0.042
6160	N-EST76b	629	541	290	272	3279	162	181	23.69	0.094
6161	N-EST76b	347	352	198	704	3214	145	154	16.00	0.048
6162	N-EST76b	483	226	183	581	2912	148	146	10.35	0.086
5986	non-GOI	148	73	285	364	3107	98	85	6.29	0.045
5987	non-GOI	652	32	280	544	2111	124	75	7.62	0.040
5988	non-GOI	232	22	186	199	1420	124	95	8.48	0.036
5989	non-GOI	123	55	256	354	2904	107	108	9.20	0.045
Avg	N-EST76a	355	269	336	430	2608	215	149	12.56	0.060
	(excl. 6174)
Avg	N-EST76b	575	396	246	568	3198	141	167	16.03	0.059
Avg	non-GOI	289	46	252	365	2386	114	91	7.90	0.041

Example 5

Generation of N-EST213 Antibodies

Synthetic peptides were generated to match the N-terminal fragment of N-EST213 (1^st20 amino acids of SEQ ID NO.3) and the C-terminal fragment of N-EST213 (last 20 amino acids of SEQ ID NO.3). These peptides are used to immunize rabbits using methods known in the art for the purpose of generating polyclonal antibodies against N-EST213 peptide.

Example 6

Generation of Transgenic Maize Events Using the N-EST213 Gene and Nitrogen Assimilation in Maize Plants Expressing N-EST213 (T0 Plants)

Generation of Transgenic Maize Plants that Overexpress the N-EST213 Protein
The plant transformation vector pAX2411 was constructed to direct overexpression of the N-EST213 protein in maize as described in a previous Example. The vector pAX2411 was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX2411 to recombine in vivo to create a vector that can direct insertion of the N-EST213 cassette into the maize genome. The formation of this recombinant vector (pAG2411) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strain containing pAG2411 was co-cultivated with maize embryos using methods known in the art. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Surprisingly, some of the plants transformed with the N-EST213 DNA were found to display an unusual phenotype. These plants were significantly shorter than non-transformed plants, with “nodal compression” present along the stalk. Seven of the 20 plants in this study exhibited this “short” phenotype. An additional 8 plants were scored as “medium” height, and an additional 4 plants were scored as “tall” height. The shorter plants developed a tassel and an ear, but both organs were sometimes undersized, and the husks were sometimes discolored or not completely formed.
Nitrogen Assimilation in Maize Plants Expressing N-EST213
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 23 transgenic plants containing the N-EST213 gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. The results of these nitrogen assays are shown below in Table 3.

TABLE 3

Nitrogen levels, N-EST213 maize events, 4 weeks following transfer to soil

2811	N-EST213	242				644	697	72	3.10	0.101
2812	N-EST213	158				618	541	30	1.99	0.078
2813	N-EST213	245	268	15		798	416	63	9.10	0.045
2814	N-EST213	296		49	77	1124	484	124	2.40	0.081
2815	N-EST213	202			62	1133	546	127	4.69	0.097
2816	N-EST213	616		27	66	1977	720	179	17.35	0.052
2817	N-EST213	6915	119	216	125	1464	509	230	14.48	0.057
2818	N-EST213	9380		221	81	2413	829	228	14.08	0.119
2822	N-EST213	3483		109	50	1458	401	150	13.42	0.074
2823	N-EST213	839		79	229	2510	671	173	8.83	0.160
2824	N-EST213	328				527	421	67	1.63	0.051
2825	N-EST213	162				566	382	75	2.62	0.084
2826	N-EST213	272				394	367	50	1.27	0.119
2827	N-EST213	181				351	384	72	2.45	0.109
2828	N-EST213	163				256	416	49	1.78	0.014
2829	N-EST213	171				274	358	71	5.25	0.098
2830	N-EST213	185		15		217	368	54	2.20	0.063
2832	N-EST213	205				742	375	53	4.01	0.102
2833	N-EST213	152				354	383	53	1.89	0.057
2835	N-EST213	232		15	100	447	363	43	2.75	0.123
2837	N-EST213	249			139	666	390	43	0.14	0.061
2838	N-EST213	2997				547	418	67		0.113
2841	N-EST213	188				300	355	70	3.03	0.071
Average		214	194	83	103	860	469	93	5	0.084
Std Dev		52		83	56	676	136	68	5.69	0.033
CV		0.24	0.00	1.01	0.54	0.79	0.29	0.73	1.06	0.39
# plants	23	23	2	9	9	23	23	23	22	23
with
positive
values
		2816 to
		2823, 2838
		excluded

Control samples were also generated from transgenic maize plants that contained the selectable marker cassette only (no N-EST213). These samples were likewise sampled at 4 weeks, and the nitrogen levels were determined. These data are shown in Table 4.

TABLE 4

Nitrogen levels, non-GOI plants, 4 weeks following planting

2760	non GOI	24939		257	92	1423	551	151	16.77	0.022
2761	non GOI	7159		196	74	1151	607	146	17.59	0.038
2762	non GOI	1625	146	225	58	1177	445	141	13.33	0.036
2763	non GOI	4421		197	119	1172	487	111	11.08	0.038
2765	non GOI	1901		131	69	874	366	92	9.10	0.032
2766	non-GOI	233		14		184	352	56	5.33	0.085
2768	non-GOI	210		9		256	346	64	5.54	0.062
2769	non-GOI	245		17		249	481	56	4.08	0.055
Average		229	146	131	83	811	454	102	10	0.046
Std Dev		18		104	24	503	96	41	5	0.020
CV		0.08		0.79	0.29	0.62	0.21	0.40	0.51	0.44
# plants with	8	3	1	8	5	8	8	8	8	8
positive
values

Example 7

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST45 (T0 and T1 Plants)

Generation of Transgenic Maize Plants that Overexpress the N-EST45 Protein
As described in the previous Example, the plant transformation vector pAX3404 was constructed to direct overexpression of the N-EST45 protein in maize.
The vector pAX3404 was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX3404 to recombine in vivo to create a vector that can direct insertion of the N-EST45 cassette into the maize genome. The formation of this recombinant vector (pAG3404) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strain containing pAG3404 was co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Nitrogen Assimilation in Maize Plants Expressing N-EST45
Nitrogen Assays, T0 Events
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 16 transgenic plants containing the N-EST45 gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. Included alongside in the analysis were plants that were transformed with a construct containing only the selectable marker (no N-EST45). These plants were likewise sampled at 4 weeks and are referred to as “non GOT” plants. The results of the nitrogen assays carried out on both types of plants are shown below in Table 5.

TABLE 5

Nitrogen levels, N-EST45 vs. non GOI maize events, 4 weeks following transfer to soil

3751	N-EST45	216	178	155	102	1383	403	84	1.30	0.074
3752	N-EST45	251		129	317	1485	407	104	1.34	0.092
3754	N-EST45	457	446	402	557	3378	768	240	2.59	0.104
3755	N-EST45	293	416	321	645	2143	484	144	1.81	0.065
3759	N-EST45	656		211	379	2068	413	135	1.73	0.051
3760	N-EST45	7172	221	238	661	2421	627	184	1.88	0.092
3762	N-EST45	809		150	273	1752	369	128	1.24	0.090
3764	N-EST45	233		108	203	1919	301	106	0.86	0.073
3765	N-EST45	598		121	284	1409	437	112	1.47	0.137
3768	N-EST45	271		118	321	1430	321	116	1.14	0.052
3771	N-EST45	480	117	189	462	1221	525	129	1.89	0.183
3772	N-EST45	565	231	167	395	2083	410	111	1.05	0.076
3773	N-EST45	659		105	263	1634	445	101	1.63	0.088
3779	N-EST45	533	96	138	354	1745	397	126	0.99	0.095
3781	N-EST45	500	109	144	286	1477	490	137	1.28	0.094
3784	N-EST45	1209	90	144	228	1446	424	135	1.11	0.089
2771 (non-GOI)	non-GOI	354		224	132	1065	506	117	0.88	0.073
2773 (non-GOI)	non-GOI	183		188	209	1040	365	109	1.27	0.044
2774 (non-GOI)	non-GOI	135		223	158	629	470	102	1.38	0.045

Average (GOI)

466

212

177

358

1812

451

131

1.46

0.091

Std Dev	187	135	82	156	537	115	37	0.44	0.032
CV	0.40	0.64	0.46	0.43	0.30	0.25	0.28	0.30	0.35
	3760, 3784
	excluded

Nitrogen Assays, T1 Events
The nitrogen levels present in the T0 N-EST45 maize events were examined and several plants were selected for characterization as T1 plants. Events (“plant #”) 3755, 3759, 3760, 3765, 3773 and 3781 were chosen. Non-GOI events 3822 and 3828 were selected as negative controls. To generate T1 plants, pollen was collected from each of the T0 events and used to pollinate ears on Hi-II (A188×B73) plants. Following seed set and seed harvest, dried seeds from these crosses were germinated in soil. Approximately 2 weeks after planting, segregants containing the N-EST45 gene (or selectable marker gene in non-GOI plants) were identified and grown until 4 weeks of age. Leaf samples were taken from these events at 4 weeks and entered into the same nitrogen testing scheme utilized for the T0 plants (nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein). The results of these nitrogen assays are shown in Table 6.

TABLE 6

Nitrogen levels, T1 plants, N-EST45 vs. non-GOI events

Average (GOI)

466*

212

177

358

1812

451

131

1.46

0.091

Std Dev		187*	135	82	156	537	115	37	0.44	0.032
CV		0.40*	0.64	0.46	0.43	0.30	0.25	0.28	0.30	0.35

Average (non GOI)

224

undet

211

166

911

447

110

1.17

0.054

Std Dev	115	20	39	245	73	8	0.26	0.017
CV	0.52	0.10	0.23	0.27	0.16	0.07	0.22	0.31

*3760, 3784 excluded

Example 8

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST61

As described in the previous Example, the plant transformation vector pAX2422 was constructed to direct overexpression of the N-EST61 protein in maize.
The vector pAX2422 was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX2422 to recombine in vivo to create a vector that can direct insertion of the N-EST61 cassette into the maize genome. The formation of this recombinant vector (pAG2422) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strain containing pAG2422 was co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Nitrogen Assimilation in Maize Plants Expressing N-EST61
Nitrogen Assays, T0 Events
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 8 transgenic plants containing the N-EST61 gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. Included alongside in the analysis were plants that were transformed with a construct containing only the selectable marker (no N-EST61). These plants were likewise sampled at 4 weeks and are referred to as “non GOT” plants. The results of the nitrogen assays carried out on both types of plants are shown below in Table 7.

TABLE 7

Nitrogen levels, N-EST61 vs. non GOI maize events, 4 weeks following transfer to soil

5629	N-EST61	205	79	267	287	1954	204	71	25.29	0.095
5630	N-EST61	790	59	223	976	2371	202	98	18.91	0.092
5632	N-EST61	222	144	266	651	2630	292	100	12.41	0.076
5633	N-EST61	193	64	314	1132	1738	387	80	8.88	0.067
5635	N-EST61	383	54	202	574	1431	248	72	8.37	0.080
5636	N-EST61	449	67	349	594	1545	402	87	9.93	0.042
5637	N-EST61	354	292	368	389	2519	244	116	20.12	0.127
5638	N-EST61	1477	37	292	835	1360	224	84	8.51	0.051
5983	non-GOI	345	61	264	71	1435	215	296	7.98	0.107
5984	non-GOI	213	155	850	398	3670	117	355	14.11	0.081
5985	non-GOI	212	73	199	566	2039	182	294	2.67	0.058

Average (N-EST61)	509	100	285	680	1943	275	89	14.05	0.079
Average (non-GOI)	256	96	438	345	2381	171	315	8.25	0.082

Example 9

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST15

As described in the previous Example, the plant transformation vector pAX2437 was constructed to direct overexpression of the N-EST15 protein in maize.
The vector pAX2437 was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX2437 to recombine in vivo to create a vector that can direct insertion of the N-EST15 cassette into the maize genome. The formation of this recombinant vector (pAG2437) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strain containing pAG2437 was co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Nitrogen Assimilation in Maize Plants Expressing N-EST15
Nitrogen Assays, T0 Events
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 8 transgenic plants containing the N-EST15 gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. Included alongside in the analysis were plants that were transformed with a construct containing only the selectable marker (no N-EST15). These plants were likewise sampled at 4 weeks and are referred to as “non GOT” plants. The results of the nitrogen assays carried out on both types of plants are shown below in Table 8.

TABLE 8

Nitrogen levels, N-EST15 vs. non GOI maize events, 4 weeks following transfer to soil

5923	N-EST15	111	245	267	1036	3244	142	321	10.41	0.074
5924	N-EST15	401	470	330	685	3271	142	349	8.65	0.056
5926	N-EST15	554	65	202	308	2376	183	327	9.22	0.072
5929	N-EST15	591	256	238	1551	2562	168	338	9.98	0.053
5930	N-EST15	1873	909	477	3059	2495	174	458	12.98	0.065
5931	N-EST15	2275	382	268	1023	3590	196	357	6.42	0.073
5932*	N-EST15	414	1107	739	1751	4049	430	683	16.79	0.125
5934	N-EST15	272	290	293	863	2306	163	312	7.37	0.047
5983	non-GOI	345	61	264	71	1435	215	296	7.98	0.107
5984	non-GOI	213	155	850	398	3670	117	355	14.11	0.081
5985	non-GOI	212	73	199	566	2039	182	294	2.67	0.058

Average (N-EST15)	811	465	352	1285	2987	200	393	10.23	0.071
Average (non-GOI)	256	96	438	345	2381	171	315	8	0.082

*5932 water content measured higher than others (93% vs. avg of 85%); also extremely fibrous and easily shredded

Example 9

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST28

As described in the previous Example, the plant transformation vector pAX2439 was constructed to direct overexpression of the N-EST28 protein in maize.
The vector pAX2439 was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB 1, which allows pSB 1 and pAX2439 to recombine in vivo to create a vector that can direct insertion of the N-EST28 cassette into the maize genome. The formation of this recombinant vector (pAG2439) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strain containing pAG2439 was co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.
Nitrogen Assimilation in Maize Plants Expressing N-EST28
Nitrogen Assays, T0 Events
A series of assays that quantify nitrogen intermediates in plants have been developed. These assays were utilized here to analyze a total of 5 transgenic plants containing the N-EST28 gene. Each of the plants was sampled following 4 weeks of growth in soil in a greenhouse. These leaf samples were processed to determine their nitrate, asparagine, glutamine, aspartic acid, glutamic acid, ammonium, total amino acid, chlorophyll and total protein levels. Included alongside in the analysis were plants that were transformed with a construct containing only the selectable marker (no N-EST28). These plants were likewise sampled at 4 weeks and are referred to as “non GOT” plants. The results of the nitrogen assays carried out on both types of plants are shown below in Table 9.

TABLE 9

Nitrogen levels, N-EST28 vs. non GOI maize events, 4 weeks following transfer to soil

6179	N-EST28	230	393	385	458	3209	116	137	15.22	0.026
6180	N-EST28	282	392	415	151	3613	126	175	22.09	0.074
6182	N-EST28	271	132	248	340	2722	133	103	8.77	0.050
6183	N-EST28	244	177	291	1098	2976	122	113	9.59	0.088
6184	N-EST28	183	253	325	496	3143	123	119	11.40	0.050
5986	non-GOI	148	73	285	364	3107	98	85	6.29	0.045
5987	non-GOI	652	32	280	544	2111	124	75	7.62	0.040
5988	non-GOI	232	22	186	199	1420	124	95	8.48	0.036
5989	non-GOI	123	55	256	354	2904	107	108	9.20	0.045
Avg	N-EST28	242	270	333	509	3133	124	129	13.41	0.057
Avg	non-GOI	289	46	252	365	2386	114	91	7.90	0.041

Example 11

Generation of Transgenic Maize Events and Nitrogen Assimilation in Maize Plants Expressing N-EST88, N-EST42, N-EST31, N-EST264

As described in the previous Example, the plant transformation vectors pAX2424 (N-EST88), pAX2435 (N-EST42), pAX2441 (N-EST31) and pAX2437 (N-EST264) were constructed to direct overexpression of the N-EST88, N-EST42, N-EST31 and N-EST264 proteins in maize.
Each vector was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB1, which allows pSB1 and pAX2424, pAX2435, pAX2441 or pAX2437 to recombine in vivo to create a vector that can direct insertion of the N-EST28 cassette into the maize genome. The formation of these recombinant vectors (pAG2424, pAG2435, pAG2441 or pAG2437) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The Agrobacterium strains containing pAG2424, pAG2435, pAG2441 or pAG2437 were co-cultivated with maize embryos using methods known in the art. Following co-cultivation, the embryos were grown on selection medium. Individual events that survived selective growth in the presence of the selection agent were then moved to regeneration medium and grown to the plantlet stage using methods known in the art.

Example 12

Generation of Plasmids to Direct Overexpression of the N-EST43, N-EST13A, N-EST13E or N-EST55C Proteins in Transgenic Maize Events

As described in the previous Example, the plant transformation vectors pAX2443 (N-EST43), pAX2454 (N-EST13A), pAX2457 (N-EST13E) and pAX2460 (N-EST55C) were constructed to direct overexpression of the N-EST43, N-EST13A, N-EST13E or N-EST55C proteins in maize.
Each vector was introduced into an Agrobacterium tumefaciens strain by electroporation. This strain also contained the vector pSB1, which allows pSB1 and pAX2443, pAX2454, pAX2457 or pAX2460 to recombine in vivo to create a vector that can direct insertion of the N-EST43, N-EST13A, N-EST13E or N-EST55C cassette into the maize genome. The formation of these recombinant vectors (pAG2443, pAG2454, pAG2457 or pAG2460) was confirmed by Southern blot hybridization of this Agrobacterium strain.
The foregoing description and drawings comprise illustrative embodiments of the present inventions. The foregoing embodiments and the methods described herein may vary based on the ability, experience, and preference of those skilled in the art. Merely listing the steps of the method in a certain order does not constitute any limitation on the order of the steps of the method. The foregoing description and drawings merely explain and illustrate the invention, and the invention is not limited thereto. Those skilled in the art who have the disclosure before them will be able to make modifications and variations therein without departing from the scope of the invention.

SEQUENCE LISTING
SEQ ID NO: 1
TCGACTGGAGCACGAGGACACTGACATGGACTGAAGGAGTAGAAAATCACCTAGCTAGAAAGGAGAGCAC

CGAGCGCTGCACCACTACTGCTGATATGAGCACCTGAACCTTCTGGGCAACCACATCGTCCCTGCCCCTG

ATCATCCGCAGCAGCCATGGCGCAGCAGCAGGAGAAGAAGCAGCAGCAGAGGGGGAAGCTGCAGAGGGTG

CTAAGGGAGCAGAAGGCTCGGCTCTACATCATCCGCCGATGCGCGTCATGCTCCTCTGCTGGAGTGACTG

ATCCATCTCAAGCATGCATGATAAACCTGTGCTCTTTTTTTTTCCTTCTGTTTTTTCCCCTCTTTTTCCC

ATCCTTTTCACCTTGCCACTTTGGTGGGCG

SEQ ID NO: 2
ATGGCGCAGCAGCAGGAGAAGAAGCAGCAGCAGAGGGGGAAGCTGCAGAGGGTGCTAAGGGAGCAGAAGG

CTCGGCTCTACATCATCCGCCGATGCGCGTCATGCTCCTCTGCTGGAGTGACTGA

SEQ ID NO: 3
MAQQQEKKQQQRGKLQRVLREQKARLYIIRRCVVMLLCWSD

SEQ ID NO.: 4
ATGTGCATTGCTGCATGGATTTGGCAGGCTCACCCTGTGCACCAACTCCTCCTGCTTCTCAACAGAGATG

AGTTCCACAGCAGGCCTACAAAAGCAGTAGGATGGTGGGGTGAAGGCTCAAAGAAGATCCTTGGTGGCAG

GGATGTGCTTGGTGGAGGAACATGGATGGGGTGCACCAAGGATGGAAGGCTTGCCTTCCTGACCAATGTG

CTTGAACCAGATGCCATGCCCGGTGCACGGACTAGGGGAGATCTGCCTCTCAAATTCCTGCAGAGCAACA

AGAGCCCACTCGAAGTTGCAACTGAAGTGGCAGAAGAAGCTGATGAATACAATGGCTTCAACCTCATACT

AGCTGATCTAACAACAAATATCATGGTTTATGTGTCAAACCGGCCTAAGGGTCAGCCTGCAACAATTCAA

CTCGTGTCACCAGGACTCCATGTGCTGTCCAATGCAAGGCTAGATAGCCCTTGGCAGAAGGCAATTCTCC

TCGGTAAAAACTTCAGGGAGCTTCTTAGGGAGCATGGTGCTGATGAGGTTGAAGTGAAGGATATAGTTGA

GAGGCTAATGACTGACACCACAAAGGCTGACAAAGATAGACTGCCAAACACTGGTTGTGATCCCAACTGG

GAGCATGGTCTGAGCTCCATCTTCATTGAGGTGCAAACTGACCAAGGGCCCTATGGGACACGGAGCACAG

CCGTTTTATCAGTGAACTATGATGGCGAAGCTAGCTTGTACGAGAAGTATCTTGAGAGTGGTATATGGAA

GGATCACACAGTGAGTTACCAGATAGAGTAG

SEQ ID NO: 5
MCIAAWIWQA HPVHQLLLLL NRDEFHSRPT KAVGWWGEGS KKILGGRDVL GGGTWMGCTK

DGRLAFLTNV LEPDAMPGAR TRGDLPLKFL QSNKSPLEVA TEVAEEADEY NGFNLILADL

TTNIMVYVSN RPKGQPATIQ LVSPGLHVLS NARLDSPWQK AILLGKNFRE LLREHGADEV

EVKDIVERLM TDTTKADKDR LPNTGCDPNW EHGLSSIFIE VQTDQGPYGT RSTAVLSVNY

DGEASLYEKY LESGIWKDHT VSYQIE

SEQ ID NO: 6
ATTCCCGTCTTACCTAGCGCTAGGGTTAGTACGCGTCCACGGCGACGACCTCTGCGCGGAGTGTGCTCCG

ATTGGCTGGCCTCCTCGATCCTCCTTCCCGCGAACGCACGCGCGCGCGAGGGAGAGGTTGAGACTTGAGA

GATAGACGAAAGACGAAACAAGGGAAGGAGACGCCGTGCTCGCCTATTGGCCGCCGCCTCCGCTCCTTCG

CGCCCAATGGCTTCTGCAGCATATCAATATCATGCAGCATAGCAGTACTCAGACCCTTACTACGCAGGCG

TTGTTGCTCCCTATGGAAGTCAAGATGTGTGTCCGAGGAGCCTGTCTATGTGAACGCCAAGCAGTACCGC

GGCATTCTAAGACGGCGGCAGTCACGTGCCAAGGCCGAGCTTGAGAGAAAGCGCTGGTCAAAGCAAGAAA

GCCGTATCTTCACGAGTCCCCGTCATCAGCACGCGATGACGAGGAGGGCGAGAGGGAACGGTGGACGCTT

CCTAAACACGAAGAAGAGTGACCGTGTCCCTCCTGATGACTTGATACAGCTACGACGACACAACGAGGCT

TGAAGAGGTAGCGGTCTGGCTGGCATCCTAGAGCAGCGGTTTCTGTCCACAGGCACGTGCATCTGAGACC

GGATCCGTAGCTCCACTCCACAGCATATGCGCAGCCCATCCATCTCGTGCACACTTG

SEQ ID NO: 7
ATGCAGCATAGCAGTACTCAGACCCTTACTACGCAGGCGTTGTTGCTCCCTATGGAAGTCAAGATGTGTG

TCCGAGGAGCCTGTCTATGTGAACGCCAAGCAGTACCGCGGCATTCTAAGACGGCGGCAGTCACGTGCCA

AGGCCGAGCTTGA

SEQ ID NO: 8
MQHSSTQTLT TQALLLPMEV KMCVRGACLC ERQAVPRHSK TAAVTCQGRA

SEQ ID NO: 9
TTGAGAGATAGACGAAAGACGAAACAAGGGAAGGAGACGCCGTGCTCGCCTATTGGCCGCCGCCTCCGCT

CCTTCGCGCCCAATGGCTTCTGCAGCATATCAATATCATGCAGCATAGCAGTACTCAGACCCTTACTACG

CAGGCGTTGTTGCTCCCTATGGAAGTCAAGATGTGTGTCCGAGGAGCCTGTCTATGTGAACGCCAAGCAG

TACCGCGGCATTCTAAGACGGCGGCAGTCACGTGCCAAGGCCGAGCTTGAGAGAAAGCGCTGGTCAAAGC

AAGAAAGCCGTATCTTCACGAGTCCCCGTCATCAGCACGCGATGACGAGGAGGGCGAGAGGGAACGGTGG

ACGCTTCCTAAACACGAAGAAGAGTGACCGTGTCCCTCCTGATGACTTGATACAGCTACGACGACACAAC

GAGGCTTGA

SEQ ID NO: 10
LRDRRKTKQG KETPCSPIGR RLRSFAPNGF CSISISCSIA VLRPLLRRRC CSLWKSRCVS

EEPVYVNAKQ YRGILRRRQS RAKAELERKR WSKQESRIFT SPRHQHAMTR RARGNGGRFL

NTKKSDRVPP DDLIQLRRHN EA

SEQ ID NO: 11
ATGACTGCTCACCAGACTTGCTGCGATGATGCCGTTGCCGCCGGCACTGCACCGGCTGCC

AGGAGGAGGCGCCTCAAATTGACGAGGCCGTCGGCCTCGCTCTTGATGGCGAGGAAGCTA

AGGAAGAAGGCTGCCGGCAGCAAACGCCCAAGGGCGGCAGCGTCGAGGAAGCGCGCGATG

GCGATCAGGAGGAAGATGGAAGCGCTGAGGCTGCTCGTGCCACTCTGCGGCCGAGACAAC

GGCTCGGTGACCGGTGGGGCGGTCGAACGACTGGACGAGCTCCTCATGCACGCCGCCGGG

TACATCCTGCGCCTCCAGATGCAGGTCAGAGTGATGCAGCTTATGGTCCATGCACTAAAT

GACCGGCCCGAGGATTAA

SEQ ID NO: 12
MTAHQTCCDDAVAAGTAPAARRRRLKLTRPSASLLMARKLRKKAAGSKRPRAAASRKRAMAIRRKMEALR

LLVPLCGRDNGSVTGGAVERLDELLMHAAGYILRLQMQVRVMQLMVHALNDRPED

SEQ ID NO: 13
ATGTCGGCGGCGCTCGCGGTGACGGACGAGGTGGCCCTGCCGATCCGGGCGGTGGGGGAT

CTAGCGGCCGCCGCCGAGGTCTCGCGGGAGGAGGTCGCCGTCATCACCCAGTGCGCGGCG

CTCGGTGGGAAGTTGCCTTTTGAAGATGCATCAGTTGGTGCGGTTCTTGCAGTCATTAAA

AACGTGGAAAGCTTGAGGGAGCAATTGGTTGCTGAAATCAGGCGGGTGCTGAAAGCTGGT

GGAAGAGTATTGGTGCAGAGCCCTGCACCCTCATCCAGTCAGAAGCCGAACACTGATATT

GAGCGCAAGTTACTGATGGGTGGATTTGCTGAAGTGCAATCTTCTGCTGCAAGCTCGCAG

GATAGCGTGCAATCTGTTACAGTTAAGGCAAAGAAGGCTAGCTGGAGCATGGGCTCTTCT

TTTCCCCTTAAGAAAACAACAAAAGCCCTTCCCAAGATTCAAATTGACGACGACTCTGAT

CTGATTGATGAAGACAGTCTCTTGACTGAGGAGGACCTGAAGAAACCACAACTTCCAGTT

GTTGGGGACTGTGAGGTGGGGGCAGCAAAGAAAGCATGCAAGAACTGTACTTGTGGCAGG

GCTGAGGCCGAGGAGAAGGTTGGGAAGCTGGAGCTCACTGCGGAGCAGATCAATAACCCT

CAGTCAGCTTGTGGCAGTTGTGGGTTGGGTGATGCCTTCCGCTGTGGAACCTGTCCCTAC

AGAGGTCTTCCACCATTCAAGCCTGGCGAGAAGGTTTCCTTGTCTGGCAACTTCCTTGCT

GCTGACATATGA

SEQ ID NO: 14
MSAALAVTDEVALPIRAVGDLAAAAEVSREEVAVITQCAALGGKLPFEDASVGAVLAVIKNVESLREQLV

AEIRRVLKAGGRVLVQSPAPSSSQKPNTDIERKLLMGGFAEVQSSAASSQDSVQSVTVKAKKASWSMGSS

FPLKKTTKALPKIQIDDDSDLIDEDSLLTEEDLKKPQLPVVGDCEVGAAKKACKNCTCGRAEAEEKVGKL

ELTAEQINNPQSACGSCGLGDAFRCGTCPYRGLPPFKPGEKVSLSGNFLAADI

SEQ ID NO: 15
ATGGCGATGCAGACGGGGGTCGCGACCTCCAAGGTCCTCATCCTCGTCGGTGCAGGGATGACGGGCTCGA

TCCTGCTGCGGAATGGCCGCTTATCTGATGTGTTGGGAGAACTCCAGGAGATTATGAAGGGTGTAAATCA

AGGAACTTCTTCGGGTCCCTATGACATTGCACTTATTCAAGCTCAGATTCGGAATTTAGCGCAAGAAGTC

AGAGATTTGACATTGTCAAAGCCCATTACCATACTGAATGGCAAATCTGACTCGGGAGGCAGTTTATCAT

CCTACATACTGCCAGCAGCAGCAGTTGGAGCAATGGGTTATTGCTACATGTGGTGGAAGGGGTTGTCTCT

CTCAGATGTCATGTTTGTCACAAAACACAACATGGCAAATGCTGTTCAGAGCATGTCAAAGCAGTTGGAG

CAAGTTTCATCAGCACTAGCTGCAACAAAAAGACATCTAACTCAACGGCTTGAGAATTTGGATGGCAAAA

TGGATGAACAAGTAGAGGTCTCCAAAGCTATTAGAAATGAGGTCAATGATGTTAAAGATGACCTGTCTCA

AATTGGATTTGATGTCGAATCAATTCAGAAAATGGTTGCTGGATTGGAGGGAAAGATCGAGTTACTTGAG

AACAAACAGGACGTGGCTAATACTGGTATCTGGTATCTCTGCCAAGTAGCAGGCGGTTTAAAAGATGGAA

TAAACACCAGGTTTTTCCAGGAAACCAGTGAGAAGCTGAAGCTCTCACATTCAGCTCAACCTGAAAACAA

GCCAGTGAAGGGGCTTGAATTTTTTTCGGAAAGCACCATGGAACAGAAAGTAGCTGACTCCAAACCAATT

GCGGTGACAGTCGACGCTGAGAAGCCTGAGAAAACCGCTGCTGTAATGGGCACCACAGTGCACAGGTCTA

TCAGGTTCTCATATCGGAAGGCAGGCCTTGCTTTGTGA

SEQ ID NO: 16
MAMQTGVATS KVLILVGAGM TGSILLRNGR LSDVLGELQE IMKGVNQGTS SGPYDIALIQ

AQIRNLAQEV RDLTLSKPIT ILNGKSDSGG SLSSYILPAA AVGAMGYCYM WWKGLSLSDV

MFVTKHNMAN AVQSMSKQLE QVSSALAATK RHLTQRLENL DGKMDEQVEV SKAIRNEVND

VKDDLSQIGF DVESIQKMVA GLEGKIELLE NKQDVANTGI WYLCQVAGGL KDGINTRFFQ

ETSEKLKLSH SAQPENKPVK GLEFFSESTM EQKVADSKPI AVTVDAEKPE KTAAVMGTTV

HRSIRFSYRK AGLAL

SEQ ID NO: 17
ATGTGCTCGGTAGCGAGGCTGGCGTTTGTGCTTGCACTGGCCATAGCCGCCTCGTCAATTGAGGTTGCGG

AGAGCAGAGATTTTAATATCTTTGCTCAGGGCAGCTTGCCTGATGCAACCAAGGGATCGTCTGGTCTAGC

TGCAACCAGTGGAAAGTTGTGTCAGTTATGCGAGCAGTACTCATCCGAGGCGCTCCTCTATCTCACACAA

AACGAGACCCAGACTGAGATTCTTAGCATTCTACACCATGAATGTGCCAGCCTTGCCCCTCTCAAACAGC

AGTGCATCACGCTGGTTGACTACTACGTACCCCTTTTCTTCTTGGAGGTCTCCATGGTTACCCCTGAGAA

GTTCTGCGAGTCGATGCATCTCTGCAAGAAGGGGATGAAGATTAGCCTACCCACCCGGGAGGGTACTTGT

GGTTTGTGCCACCATGTTGTTGTTGAAATTCTTATCATGCTTAAAGACCCCAACATGCAGCTGGAAGTAA

TCGACCTACTCACCAAAACATGCAGCAAGGCGCAGAACTATGAACAGTAG

SEQ ID NO: 18
MCSVARLAFV LALAIAASSI EVAESRDFNI FAQGSLPDAT KGSSGLAATS GKLCQLCEQY

SSEALLYLTQ NETQTEILSI LHHECASLAP LKQQCITLVD YYVPLFFLEV SMVTPEKFCE

SMHLCKKGMK ISLPTREGTC GLCHHVVVEI LIMLKDPNMQ LEVIDLLTKT CSKAQNYEQ

SEQ ID NO: 19
GGACACTGACATGGACTGAAGGAGTAGAAAATCCATCCATTCCCCTCGCCAAGCCGCCACGGCCTGACTT

TCCCTCCCGCACACCCGCGACCATACAGGCAAGTCAGGCATACACCAACAACGCTCGTCGTGCACCTCGC

GCCTCAGGTCACCCCACCAAATTCCTCTTGATACGCCGAATTTCTTTTGCTAATTCTGCTACCTCCTGTC

GCTAAGCCACCATATTCAGTCTAACCCCTGCTCTGAGCTCACCTGATTGGCGGCTCCGTTCGGCCTCTGG

GCCTGGGTGTACCGACTACCGAGGGCTCTTTCGAAATGTCAATTGGGTCGAGTTTGGTGGGCTACGTGAA

GCATGGATGAATTTCCCGGCTGGAAGCGGGAGGCGGCAGCAGCATCCGGGGCCGGAGCACCTGTCGCCGA

TGACGCCGCTCCCGCTGGCGCGGTAGGGGTCGGTCTACTCGCTCACGTTCGACGAGTTCCAGAGCTCGCT

CGGTGGGGCCACCAAGGACTTCGGATCCATGAACATGGACGAGCTCCTCCGCAACATCTGGTCGGCGGAG

GAGACACACAGCGTCACAGCTGCGGACCATGCCGCGCGGGCGCCGTACGTCCAGTGCCAGGGCTCGCTCA

CCCTCCCCTGCACGCTCAGCCAGAAGACCGTCGACGAGGTCTAGCGTGACCTCGTGTGCAACGGTGGAGG

ACCCTCCGACGAGGCTGTGGCGCCGCCCCACCGGCCCAACGGCAGCCGACGCTCGGGGAGATCATGCTGG

AGGAGTTCCTCGTCCGCGCCGGCGTGGTGAGGGAGGACATGATGGCGGCGGCGCCCGTACCACCAGCGCC

GGGTTGCCCACCACCTCATCTGCAACCGCCAATGCTGTTTCCACATGGCAATGTGTTTGCTCCCTTAGTG

CCTCCGCTCCAATTCGGGAATGGGTTTGTGTCGGGGGCTCTCAGTCAGCAGCAGGGAGGTGTTCTTGAGG

CCCCGGCGGTATCGCCGCGGCCGGTGACGGCAAGCGGGTTCGGGAAGATGGAAGGAGACGACTTGTCGCA

TCTGTCGCCATCACCGGTGTCGTACGTTTTTTTGTGCTGGTTTGAGGGGAAGGAAGCCACCAGCTGTGGA

G AAGGTGGTTGAGAGGAGGCAACGCC

SEQ ID No: 20
mdfpggsgrq qqlppmtplp larqgsvysl tfdefqstlg gvgkdfgsmn mdellrsiwt

aeeshavgaa ttttattasv aaaehaavga ppvqrqgslt 1prtlsqktv devwrdmmcf

ggggastapa aaeppppahr qqtlgeitle eflvragvvr edmsvppvpp aptptaaavp

pppppqqqtp mlfgqsnvfp pmvpplslgn glvsgavghg gggaaslvsp vrpvssngfg

kmeggdlssl spspvpyvfk gglrgrkapg iekvverrqr rmiknresaa rsrqrkqaym

meleaevakl kelndelqkk qdemleqqkn evlermsrqv gptakriclr rtltgpw

SEQ ID NO: 21
atg gattttccgg gagggagcgg

gaggcagcag cagctgccgc cgatgacgcc gctgccgttg gcgaggcagg ggtcggtgta

ctcgctcacg ttcgacgagt tccagagcac gctgggcggg gtcgggaagg acttcgggtc

gatgaacatg gacgagctcc tccgcagcat ctggacggcc gaggagtcgc acgccgtcgg

cgccgccacg acgacgacgg cgacgacggc gtccgtggcg gcggcggagc acgcggcggt

gggggcgccg cccgttcaga ggcaggggtc gctgaccctc ccccgcacgc tcagccagaa

gaccgtcgac gaggtctggc gcgacatgat gtgcttcggt ggcggcggcg cctccaccgc

gccggccgcc gcggagcccc cgccgccggc gcaccggcag cagacgctcg gggagatcac

gctggaggag ttcctcgtgc gggccggcgt ggtgagggag gacatgtcgg tcccgcccgt

cccgccggcg ccgactccta cggcggctgc tgtacctccc ccgccgccgc cgcagcagca

gacgccgatg ttgttcggtc agagcaatgt gttccctccg atggtgcctc cgctctcgct

gggaaatggg ctggtctcgg gagctgtcgg acacggcggt ggtggtgccg cgtcgttggt

ttcgccggtg aggccggtct cgtccaatgg cttcggcaag atggaaggcg gggacctgtc

gtcgctgtcg ccatcgccgg tgccgtacgt tttcaaaggt gggctgaggg gaaggaaggc

accgggcatc gagaaggttg tcgagagaag acagcggcgg atgatcaaga acagggagtc

tgccgcgagg tcgcgccaga ggaaacaggc atatatgatg gaattggaag ctgaggtagc

aaaacttaag gagctgaacg atgaactcca gaaaaagcag gatgaaatgt tggagcagca

aaagaatgag gttctagaga gaatgagccg acaagttgga ccgacagcaa agagaatttg

ccttcggagg actctgacgg gtccatggtg a

SEQ ID NO: 22
ATGAATTTCCCGGCTGGAAGCGGGAGGCGGCAGCAGCATCCGGGGCCGGAGCACCTGTCGCCGATGACGC

CGCTCCCGCTGGCGCGGCAGGGGTCGGTCTACTCGCTCACGTTCGACGAGTTCCAGAGCTCGCTCGGTGG

GGCCACCAAGGACTTCGGATCCATGAACATGGACGAGCTCCTCCGCAACATCTGGTCGGCGGAGGAGACA

CACAGCGTCACAGCTGCGGACCATGCCGCGCGGGCGCCGTACGTCCAGTGCCAGGGCTCGCTCACCCTCC

CCTGCACGCTCAGCCAGAAGACCGTCGACGAGGTCTGGCGTGACCTCGTGTGCAACGGTGGAGGACCCTC

CGACGAGGCTGTGGCGGCCGCCCCACCGGCCCAACGGCAGCCGACGCTCGGGGAGATCATGCTGGAGGAG

TTCCTCGTCCGCGCCGGCGTGGTGAGGGAGGACATGATGGCGGCGGCGCCCGTACCACCAGCGCCGGGTT

GCCCACCACCTCATCTGCAACCGCCAATGCTGTTTCCACATGGCAATGTGTTTGCTCCCTTAGTGCCTCC

GCTCCAATTCGGGAATGGGTTTGTGTCGGGGGCTCTCAGTCAGCAGCAGGGAGGTGTTCTTGAGGCCCCG

GCGGTATCGCCGCGGCCGGTGACGGCAAGCGGGTTCGGGAAGATGGAAGGAGACGACTTGTCGCATCTGT

CGCCATCACCGGTGTCGTACGTTTTTTTGTGCTGGTTTGAGGGGAAGGAAGCCACCAGCTGTGGAGAAGG

TGGTTGA

SEQ ID NO: 23
MNFPAGSGRR QQHPGPEHLS PMTPLPLARQ GSVYSLTFDE FQSSLGGATK DFGSMNMDEL

LRNIWSAEET HSVTAADHAA RAPYVQCQGS LTLPCTLSQK TVDEVWRDLV CNGGGPSDEA

VAAAPPAQRQ PTLGEIMLEE FLVRAGVVRE DMMAAAPVPP APGCPPPHLQ PPMLFPHGNV

FAPLVPPLQF GNGFVSGALS QQQGGVLEAP AVSPRPVTAS GFGKMEGDDL SHLSPSPVSY

VFLCWFEGKE ATSCGEGG

SEQ ID NO: 24
ATGAATTTCCCGGCTGGAAGCGGGAGGCGGCAGCAGCATCCGGGGCCGGAGCACCTGTCGCCGATGACGC

CGCTCCCGCTGGCGCGGCAGGGGTCGGTCTACTCGCTCACGTTCGACGAGTTCCAGAGCTCGCTCGGTGG

GGCCACCAAGGACTTCGGATCTATGAACATGGACGAGCTCCTCCGCAACATCTGGTCGGCGGAGGAGACA

CACAGCGTCACAGCTGCGGACCATGCCGCGCGGGCGCCGTACGTCCAGTGCCAGGGCTCGCTCACCCTCC

CCTGCACGCTCAGCCAGAAGACCGTCGACGAGGTCTGGCGTGACCTCGTGTGCAACGGTGGAGGACCCTC

CGACGAGGCTGTGGCGGCCGCCCCACCGGCCCAACGGCAGCCGACGCTCGGGGAGATCATGCTGGAGGAG

TTCCTCGTCCGCGCCGGCGTGGTGAGGGAGGACATGATGGCGGCGGCGCCCGTACCACCAGCGCCGGGTT

GCCCACCACCTCATCTGCAACCGCCAATGCTGTTTCCACATGGCAATGTGTTTGCTCCCTTAGTGCCTCC

GCTCCAATTCGGGAATGGGTTTGTGTCGGGGGCTCTCAGTCAGCAGCAGGGAGGTGTTCTTGAGGCCCCG

GCGGTATCGCCGCGGCCGGTGACGGCAAGCGGGTTCGGGAAGATGGAAGGAGACGACTTGTCGCATCTGT

CGCCATCACCGGTGTCGTACGTTTTTTTGTGCTGGTTTGAGGGGAAGGAAGCCACCAGCTGTGGACAAGG

TGGTGAGAGAAGACAGAGGAGGATGATCAAGAACAGGGAGTCTGCCGCGAGGTCGAGGCAGAGGAAACAG

GCATATATGATGGAATTGGAAGCTGAGGTAGCAAAGCTCAAGGAGCTGAACGACGAGCTCCAGAAGAAGC

AGGACGAGATGCTGGAGCAGCAGAAGAACGAGGTGCTGGAGAGGATGTCC

AGGCAGGTGGGCCCAACCGCCAAGAGGATTTGCCTGAGGAGGACCCTGACCGGCCCATGGTGA

SEQ ID NO: 25
MNFPAGSGRR QQHPGPEHLS PMTPLPLARQ GSVYSLTFDE FQSSLGGATK DFGSMNMDEL

LRNIWSAEET HSVTAADHAA RAPYVQCQGS LTLPCTLSQK TVDEVWRDLV CNGGGPSDEA

VAAAPPAQRQ PTLGEIMLEE FLVRAGVVRE DMMAAAPVPP APGCPPPHLQ PPMLFPHGNV

FAPLVPPLQF GNGFVSGALS QQQGGVLEAP AVSPRPVTAS GFGKMEGDDL SHLSPSPVSY

VFLCWFEGKE ATSCGQGGER RQRRMIKNRE SAARSRQRKQ AYMMELEAEV AKLKELNDEL

QKKQDEMLEQ QKNEVLERMS RQVGPTAKRI CLRRTLTGPW

SEQ ID NO: 26
ATGATGTTCTCCTCCTCCCTCTCTGTGGTGGAGTTTTACTTCCTGCACAGATTCCCCCTG

CCTTTTGCTGGCTACCTCATCTTCATTTCCATATTGGCTGGATTCTGGGGCCAGTGTTTG

GTTAGGAAGATCGTGCATGTGCTCAAGAGAGCATCGCTTATTGTCTTCATCCTCTCCTCT

GTTATCTTCGTCAGTGCTCTTACGATGGGTGTCGTTGGAACCCAGAAGAGCATTTCGATG

ATCAACAATCACGAATATATGGGGTTCCTCAACTTCTGCGAGTAA

SEQ ID NO: 27
MMFSSSLSVV EFYFLHRFPL PFAGYLIFIS ILAGFWGQCL VRKIVHVLKR ASLIVFILSS

VIFVSALTMG VVGTQKSISM INNHEYMGFL NFCE

SEQ ID NO: 28
ATGGCGTCTGCAGTGACCAGCAGCGACAAGGAGCAGGCCGTCCCTACCATCGACGCTGAC

GAAGCGCACGCGCTGCTGAGCTCCGGCCATGGCTACGTGGATGTCAGGATGCGGGGGGAC

TTCCACAAGGCGCATGCGCCCGGTGCTCGGAACGTTCCCTACTACCTGTCCGTCACGCCG

CAAGGGAAGGAGAAGAACCCACACTTTGTAGAGGAAGTGGCTGCCTTCTGTGGGAAGGAT

GATGTCTTCATTGTGGGTTGCAACACGGGGAACAGATCCAGGTTCGCGACGGCAGACCTT

CTGAACGCGGGGTTCAAGAACGTGAGGAACCTGCAAGGTGGTTACCGCTCCTTTCAGCAG

CGAGCTCAACAGCAGTA

SEQ ID NO: 29
MASAVTSSDK EQAVPTIDAD EAHALLSSGH GYVDVRMRGD FHKAHAPGAR NVPYYLSVTP

QGKEKNPHFV EEVAAFCGKD DVFIVGCNTG NRSRFATADL LNAGFKNVRN LQGGYRSFQQ

RAQQQ

SEQ ID NO: 30
ATGGAGGCGAAGAAGAAGCCGTCGGCCCCCGCCGCCGTCGGAGCCGCGCCGCCGCCGCCG

GGTAACGGGTACTTCAGCACCGTCTTCTCCGCGCCGACTGCGGGAAGCGCAAGTGACGCA

AAGCATGCGGACTTGTACACGATGCTGAACAAGCAGAGCTCCAGAGGGCAGAATGGCAGA

GATGGCAAATCCCACAGCCGCCCTACTTACAAGGATGGCAAACATGCTCATCCAAATGAG

CCATCAGAATCTCCTTACTTTGGCTCATCCGTGCATTACGGTGGTCGGGAGTTCTACAGC

AGCGTTTTACGGAAGCAACCAGCCAATGAACCCCATACGGATTACAAGGGGGACAACCCG

GATGGCTCTGCTACCAGAGGTGATTGGTGGCAAGGTTCACTTTATTACTGA

SEQ ID NO: 31
MEAKKKPSAP AAVGAAPPPP GNGYFSTVFS APTAGSASDA KHADLYTMLN KQSSRGQNGR

DGKSHSRPTY KDGKHAHPNE PSESPYFGSS VHYGGREFYS SVLRKQPANE PHTDYKGDNP

DGSATRGDWW QGSLYY

SEQ ID NO: 32
ATGGACCGGAACCTGAGCGGGTTTCTGATCGGGTGCCTGGGCGCCGCCGTGACGCTGCTG

GCGTACCAGCAGACGGTGGTGACCAGCACGCAGAGCGTCGCGGCGGGCTTCGTCGTCATC

CTCTTCGCCCTCTTCGTCAAGGAAGGATTCATTTCCCTCTGA

SEQ ID NO: 33
MDRNLSGFLI GCLGAAVTLL AYQQTVVTST QSVAAGFVVI LFALFVKEGF ISL

SEQ ID NO: 34
ATGGCATGCGTCAGCACCTTCCAGAGCTGCCCCATTGCCAGAAGAGCAAAGATCAACACCAGGTCCAGGG

GCAGCAGCAGTAGCGTGGCGAAGGGGTCACCACCACCAGCCTTCCAGTTCCAGTGCAGGGCGTCGACTTT

CGCGGCGGACACCAGCCTCCGGCTCGAGCTGGACGAGAACCCCGAGGCGATCATCTCGGGGGCGTGGCCC

GGGAACTGCTCCCTCCTCAGCTACGACGACCTCCGCGCCTACCTCGAGTCGCAGGAGACGGCGGCCCAGG

CAGACGATCAGCGCGGCGTGGCGCTCCTGAGCGAGACCATGTCCACACCCGTGCTGGTGGCCACAGCAGA

CCAGACCCTGGAGGACGTCGAGTGCCACTTCGAGGCCGTGTCGGGGCTTCCGGTCGTCGACAGCGGCCTC

AGATGCGTCGGGGTGATCGTCAAGAACGACCGGGCAAGAGCCTCTCATGGGTCCAAGACGAAGATATCGG

AAGTGATGACATCTCCAGCTATCACACTATCGTCTGACAAAACCGTGATGGATGCTGCTGTTCTCATGCT

CAAGAAGAAGATCCACAGATTACCAGTTGTAAACCAGGACGAAAAAGTAATAGGTATAGTTACCCGCGCT

GATGTTCTTCGCGTGTTGGAAGGCATGTTGAAGATTTAG

SEQ ID NO: 35
MACVSTFQSC PIARRAKINT RSRGSSSSVA KGSPPPAFQF QCRASTFAAD TSLRLELDEN

PEAIISGAWP GNCSLLSYDD LRAYLESQET AAQADDQRGV ALLSETMSTP VLVATADQTL

EDVECHFEAV SGLPVVDSGL RCVGVIVKND RARASHGSKT KISEVMTSPA ITLSSDKTVM

DAAVLMLKKK IHRLPVVNQD EKVIGIVTRA DVLRVLEGML KI

SEQ ID NO: 36
ATGGGCGACCTCTCTGTCGGCCACAGCCGCCGCTGGTGCGGCCGTTTCGCGGCCGTCCTTTGCCTGTGCG

CGGCCTTCTGCAAGCCAGATGAACTCCCGATGGATCCACTGCCGAACTTGCCGCCGACGAGGTCGCTGCA

GTGCTTCGAGGACGAACAGGTGTACAGCTGCTGCGAGGGCGCGTACAGGCTAAACCCATCGGGAATCATC

GCCGTTCCCGTCGGCGCGGTGGACTACTACTGCGGCGGCGCGTGCGTGGTGGAGACGGAGGACGTGCTCA

ACTGCGTGGCCAGCGCCCTGGACGGCTTCGCCTTCTACAACGGGGCCTCCGTGGAGGACGTGCGCTACGC

ACTCAGGCGGGGCTGCAGCCACACCGCCAGAAGAGGCGACTTCAACGATTTGGAGCCGCATCTGGGCGAC

TACCCTGACATCTATGGCGACGATGATGAGCACAGCTTTGGCAGCAAGGTTGTTGCAGCTCCTCTGAGGT

TGCTCGCGTTTCTTGGCGGTGCGGGGCTGTTCTTCCTGGGCCCTTGA

SEQ ID NO: 37
MGDLSVGHSR RWCGRFAAVL CLCAAFCKPD ELPMDPLPNL PPTRSLQCFE DEQVYSCCEG

AYRLNPSGII AVPVGAVDYY CGGACVVETE DVLNCVASAL DGFAFYNGAS VEDVRYALRR

GCSHTARRGD FNDLEPHLGD YPDIYGDDDE HSFGSKVVAA PLRLLAFLGG AGLFFLGP

SEQ ID NO: 38
ATGGATTCGGAGGCGGTGCAGCACGGCCTTCTCCCTCTGTCTGCCTGTCCTCCTACCGCCAACAGCTGCG

CGCATTACAGCCGTGGGTGCAGCGTCGTGGCGCCCTGCTGCGGCCAGGCCTTCGGCTGCCGCCATTGCCA

CAACGACGCCAAGAACTCGCTGGAGGTCGACCCGCGCGACCGGCACGAGATCCCCCGCCACGAAATAAAG

AAGGTGATCTGTTCTCTCTGCTCCAAGGAACAGGACGTGCAACAGAACTGCTCCAGCTGTGGGGCCTGCA

TGGGCAAGTACTTCTGTAAAGTATGCAAGTTCTTCGATGATGATGCCTCAAAGGGCCAGTACCACTGTGA

CGGATGTGGAATATGTAGAACCGGCGGCGTGGAGAACTTTTTCCACTGTGATAAATGTGGGTGTTGCTAC

AGCAATGTCTTGAAGGATTCCCACCACTGCGTCGAAAGAGCAATGCATCACAACTGCCCCGTCTGCTTTG

AGTATCTGTTCGACTCCACGAAGGACATCAGCGTGCTGCAATGTGGGCATACCATCCATTTGGAGTGCAT

GAACGAGATGAGAGCACACCATCACTTCTCATGCCCAGTGTGCTCGAGGTCCGCCTGCGACATGTCGGCC

ACATGGCGGAAGCTCGACGAGGAGGTCGCGGCCACGCCGATGCCTGACATCTACCAGAAGCACATGGTGT

GGATCCTGTGCAACGACTGCAGCGCGACCTCGAGCGTGCGGTTCCACGTGCTGGGGCACAAGTGCCCCGC

GTGCAGCTCGTACAACACCCGGGAGACGAGGGCTGCGTGCCCCAGGATCTGA

SEQ ID NO: 39
MDSEAVQHGL LPLSACPPTA NSCAHYSRGC SVVAPCCGQA FGCRHCHNDA KNSLEVDPRD

RHEIPRHEIK KVICSLCSKE QDVQQNCSSC GACMGKYFCK VCKFFDDDAS KGQYHCDGCG

ICRTGGVENF FHCDKCGCCY SNVLKDSHHC VERAMHHNCP VCFEYLFDST KDISVLQCGH

TIHLECMNEM RAHHHFSCPV CSRSACDMSA TWRKLDEEVA ATPMPDIYQK HMVWILCNDC

SATSSVRFHV LGHKCPACSS YNTRETRAAC PRI

Claims

1. A method for increasing nitrogen utilization efficiency in a plant comprising:

(a) transforming a plant cell with an expression vector comprising an isolated nucleic acid molecule that comprises a nucleotide sequence that encodes an amino acid sequence that is at least 95% identical to the sequence set forth in SEQ ID NO: 5,

(b) expressing said nucleic acid molecule in said plant cell;

(c) generating from said plant cell a transformed plant in which said nucleotide sequence is overexpressed; and

(d) selecting from a plurality of said transformed plants a plant having increased nitrogen use efficiency as compared to a control plant grown under the same conditions.

2. The method according to claim 1, said expression vector further comprising a 5′ DNA promoter sequence and a 3′ terminator sequence, wherein the nucleotide sequence, the DNA promoter sequence, and the terminator sequence are operatively coupled to permit transcription of the nucleotide sequence.

3. The method according to claim 2, wherein the promoter sequence is selected from the group consisting of constitutive plant promoters and tissue specific promoters.

4. A plant, comprising a plant produced by the method of claim 1.

5. A plant according to claim 4, wherein the plant is selected from the group consisting of corn (maize); sorghum; wheat; sunflower; crucifers; peppers; potato; cotton; rice; soybean; sugarbeet; sugarcane; tobacco; barley; oilseed rape; Brassica sp.; alfalfa; rye; millet; safflower; peanuts; sweet potato; cassaya; coffee; coconut; pineapple; citrus trees; cocoa; tea; banana; avocado; fig; guava; mango; olive; papaya; cashew; macadamia; almond; oats; vegetables; grasses; azalea, hydrangea, hibiscus, roses, tulips, daffodils, petunias, carnation, poinsettia, and chrysanthemum; and conifers.

6. Transgenic plant tissue of a plant of claim 5.

7. Transgenic plant seed produced from a plant of claim 5.

8. A host cell, comprising a host cell transformed with at least a first nucleotide sequence using the method of claim 1.

9. The host cell according to claim 8, wherein the host cell is selected from the group consisting of bacterial cells and plant cells.

10. A method of expressing a nucleic acid molecule modulated by nitrogen in a plant, said method comprising the steps of providing a transgenic plant or plant seed transformed with a vector construct according to claim 1, and growing the transgenic plant or a plant grown from the transgenic plant seed under conditions effective to express the nucleic acid molecule in said transgenic plant or said plant grown from the transgenic plant seed.

11. A method according to claim 10, wherein expression of the nucleic acid molecule is effective in increasing nitrogen uptake of said transgenic plant or said plant grown from the transgenic plant seed.

12. A method according to claim 10, wherein expression of the nucleic acid molecule is effective in increasing efficiency of nitrogen utilization of said transgenic plant or said plant grown from the transgenic plant seed.

13. A method according to claim 10, wherein the plant is selected from the group consisting of rice, corn, soybean, canola, wheat, alfalfa, barley, rye, cotton, sunflower, peanut, sweet potato, bean, pea, potato, oilseed rape, sorghum, forage grass, pasture grass, turf grass, sugarcane.

14. A method of according to claim 10, wherein expression of the nucleic acid molecule is effective in improving the stress tolerance of said transgenic plant or said plant grown from the transgenic plant seed.

15. A method according to claim 10, wherein expression of the nucleic acid molecule is effective in altering the morphology of said transgenic plant or said plant grown from the transgenic plant seed.

16. A method for increasing nitrogen utilization efficiency in a plant comprising:

(a) transforming a plant cell with an expression vector comprising an isolated nucleic acid molecule that comprises a nucleotide sequence that encodes an amino acid sequence set forth in SEQ ID NO: 5,

(b) expressing said nucleic acid molecule in said plant cell;