Patent Application
20050076412
The present invention relates to a method for modifying levels of a cell protectant, such as a cryoprotectant, an osmoprotectant or the like, in a cell to improve its response to environmental stresses, including but not limited to cold or freezing stress, drought stress or salt stress.
Due to the commercial consequences of environmental stress damage to crops, there is an interest in understanding how to improve a plant's tolerance to environmental stresses. By improving a plant's performance or survival in response to different environmental stresses, the weather-related losses in productivity and risks to farming can be greatly reduced. Modifying a plant's tolerance to environmental stresses also allows a plant to be grown in regions where a plant or plant variety is typically unable to grow.
Many biochemical changes occur in a plant when a plant becomes tolerant to an environmental stress. For example, for cold or freezing stress tolerance, it is well documented that lipid composition changes occur during cold acclimation in a wide range of plants and there is compelling data to indicate that this contributes to greater freezing tolerance (Steponkus et al. (1993) Advances in Low-Temperature Biology, Vol. 2, P. L. Steponkus, ed. (London: JAI Press), pp. 211-312).
Similarly, the levels of proline and sucrose increase in Arabidopsis (McKown et al. (1996) J. Exp. Bot. 47, 1919-1925; Wanner and Junttila (1999) Plant Physiol. 120, 391-400) and other plants (Guy et al. (1992) Plant Physiol. 100, 502-508; Koster and Lynch, (1992) Plant Physiol. 98, 108-113) during cold acclimation and likely have roles in freezing tolerance. There is evidence that proline can protect both membranes and proteins against freeze-induced damage in vitro (Rudolph and Crowe (1985) Cryobiology 22, 367-377; Carpenter and Crowe, (1988) Cryobiology 25, 244-255) and direct evidence that increased levels of proline enhances whole plant freezing tolerance (Nanjo et al. (1999) FEBS Lett. 461, 205-210).
Sucrose and other simple sugars have also been shown to be effective cryoprotectants in vitro (Strauss and Hauser (1986) Proc. Natl. Acad. Sci. USA 83, 2422-2426; Carpenter and Crowe (1988) supra) and there is correlative evidence indicating a role in freezing tolerance in cold-acclimated plants (Guy et al. (1992) supra; Koster and Lynch (1992) supra; Wanner and Junttila (1999) supra).
Similarly, tolerance to drought or water stress is associated with the accumulation of a variety of osmolytes, including sugar alcohols such as mannitol, amino acids such as proline, and glycine betaine (Greenway et al. (1980) Ann. Rev. Plant Physiol. 31: 149-190; Yancey et al. (1982) Science 217: 1214-1222).
The present invention provides a method for increasing the levels of these cell protectants in a cell to allow the cell to tolerate greater environmental stresses.
In one aspect, the present invention provides a method for modifying the level of a cell protectant in a cell. The method comprises transforming a cell with a recombinant polynucleotide comprising a sequence encoding a C-repeat/DRE binding factor (CBF)-related polypeptide and expressing the CBF-related polypeptide in the cell. Expression of the CBF-related polypeptide modifies the level of the cell protectant in the plant. The method may optionally comprise cold-acclimating the cell to increase the levels of cell protectants in the transformed cell even further.
In one embodiment, the recombinant polynucleotide encodes a CBF-related polypeptide comprising the AP2 domain comprising amino acids 45, 46, 48, 50-52, 54, 59, 60, 62, 64, 65, 67, 68, 71-73, 75-77, 79, 81, 83-91, 93-96, 99, 101, 102, and 104-106 of CBF1 (SEQ ID NO: 2).
Additionally, the recombinant polynucleotide may comprise a regulatory region operably linked to the sequence encoding the CBF-related polypeptide. The regulatory region may comprise a constitutive promoter, an inducible promoter, a tissue specific promoter or a developmental stage specific promoter. Cell protectants whose levels may be modified include proline, sugars, such as sucrose, or lipids, such as fatty acids. As a result of the increased levels of any of these cell protectants, or of a combination of any these cell protectants, the environmental stress tolerance of a cell is increased. The environmental stresses may be cold or freezing tolerance, drought tolerance or high salinity tolerance.
In a second aspect, the present invention is a method for improving the tolerance of a cell to an environmental stress. The method comprises transforming the cell with a recombinant polynucleotide comprising a sequence encoding a C-repeat/DRE binding factor (CBF)-related polypeptide and expressing the CBF-related polypeptide in the transformed cell. Expression of the CBF-related polypeptide typically increases cell protectant levels at least 1.5 fold in the transformed cell compared with cell protectant levels in an untransformed cell. The enhanced cell protectant levels improve the environmental stress tolerance of the plant.
In one embodiment, the recombinant polynucleotide encodes a CBF-related polypeptide comprising the AP2 domain comprising amino acids 45, 46, 48, 50-52, 54, 59, 60, 62, 64, 65, 67, 68, 71-73, 75-77, 79, 81, 83-91, 93-96, 99, 101, 102 and 104-106 of CBF1 (SEQ ID NO: 2). In a second embodiment, the CBF-related polypeptide may comprise one or more of the following peptides: PKXXAGR (amino acids 31-37 of SEQ ID NO: 2), or AGRXKF (amino acids 35-40 of SEQ ID NO: 2) or ETRHP (amino acids 42-46 of SEQ ID NO: 2).
Additionally, the recombinant polynucleotide may comprise a regulatory region operably linked to the sequence encoding the CBF-related polypeptide. The regulatory region may comprise a constitutive promoter, an inducible promoter, a tissue specific promoter or a developmental stage specific promoter. Cell protectants whose levels may be modified include proline, sugars, such as sucrose, or lipids, such as fatty acids. As a result of the increased levels of any of these cell protectants or the combination of any of these cell protectants, the environmental stress tolerance of a cell is improved.
In a further aspect, the present invention is a method for producing a cell protectant. The method comprises transforming a cell with a recombinant polynucleotide comprising a sequence encoding a C-repeat/DRE binding factor (CBF)-related polypeptide, expressing said recombinant polypeptide in the transformed cell so as to increase the levels of the cell protectant in the cell, and then isolating the cell protectant from the transformed cell.
Summing up the presently disclosed means by which the levels of a cell protectant in a plant cell may be modified, it has been shown that:
1. Definitions
“Environmental stress tolerance” refers to a decrease in the extent of a cell's injury or growth inhibition or an increase in survival rate after exposure to cold or freezing temperatures, drought conditions, high salinity environments or the like.
A “cell protectant” refers to a compound that improves the environmental stress tolerance of a cell. The cell protectant may be a cryoprotectant or an osmoprotectant. The cell protectant may be proline or any metabolically related compound, sugars or any metabolically related compound, and a variety of lipids, including fatty acids, which protect a cell's integrity during an environmental stress.
A “polynucleotide” is a nucleotide sequence comprising a gene coding sequence or a fragment thereof (comprising at least 18 consecutive nucleotides, preferably at least 30 consecutive nucleotides, and more preferably at least 50 consecutive nucleotides). Additionally, the polynucleotide may comprise a promoter, an intron, an enhancer region, a polyadenylation site, a translation initiation site, 5′ or 3′ untranslated regions, a reporter gene, a selectable marker or the like. The polynucleotide may comprise single stranded or double stranded DNA or RNA. The polynucleotide may comprise modified bases or a modified backbone. The polynucleotide may be genomic, a transcript (such as an mRNA) or a processed nucleotide sequence (such as a cDNA). The polynucleotide may comprise a sequence in either sense or antisense orientations.
A “recombinant polynucleotide” is a polynucleotide that is not in its native state, e.g., the polynucleotide is comprised of a nucleotide sequence not found in nature or the polynucleotide is separated from nucleotide sequences with which it typically is in proximity or is next to nucleotide sequences with which it typically is not in proximity.
A “consensus sequence”, with regard to nucleotide sequences, refers to a derived (i.e., idealized) nucleotide sequence that serves to represent a family of similar, experimentally-derived sequences. Each position in the consensus sequence is assigned a base that corresponds to the most frequently occurring nucleotide in the experimentally-derived sequences, when the real sequences are compared in an alignment.
A “transformed plant” refers to a plant that contains genetic material not normally found in a wild type plant and which has been introduced into a plant by human manipulation. A transformed plant is a plant that may contain an expression vector or cassette. The expression cassette comprises a gene coding sequence and allows for the expression of the gene coding sequence. The expression cassette may be introduced into a plant by transformation or by breeding after transformation of a parent cell. In particular, the transformed plant may refer to a whole plant as well as to a plant part, such as flower, seed, fruit, leaf, or root, plant tissue, plant cells or any other plant material, and progeny thereof.
A “transformed cell” refers to a cell that contains genetic material not normally found in a wild type cell and which has been introduced into the cell by human manipulation. A transformed cell is a cell that may contain an expression vector or cassette. The expression cassette comprises a gene coding sequence and allows for the expression of the gene coding sequence. The expression cassette may be introduced into a cell by transformation or by breeding after transformation of a parent cell. A transformed cell may refer to a cell from any organism, including mammalian cells, plant cells, bacterial cells, and the like. In particular, the transformed cell is a plant cell and may refer to a whole plant as well as to a plant part, such as seed, fruit, leaf, or root, plant tissue, plant cells or any other plant material, and progeny thereof.
The term “modified expression” in reference to polynucleotide or polypeptide expression refers to an expression pattern in the transformed cell that is different from the expression pattern in the wild type cell; for example, by expression in a cell type other than a cell type in which the polynucleotide or polypeptide is naturally expressed, or by expression at a time other than at the time the polynucleotide or polypeptide is expressed in the wild type cell, or by a response to different inducible agents, such as hormones or environmental signals, or at different expression levels (either higher or lower) compared to those observed a wild type cell. The term may also refer to lowering the levels of expression to below the detection level or completely abolishing expression. The resulting expression pattern may be transient or stable, constitutive or inducible.
A “CBF-related polypeptide or CBF” is a transcription factor that binds to a promoter comprising a cold- and dehydration-responsive DNA regulatory element known as the CRT (C-repeat)/DRE (dehydration responsive element) (Baker et al. (1994) Plant. Mol. Biol. 24:701-713; Yamaguchi-Shinozaki and Shinozaki (1994) Plant Cell 6, 251-264). These proteins comprise an AP2/EREBP DNA binding motif (Riechmann and Meyerowitz (1998) Biol. Chem. 379, 633-646) and are transcriptional activators (Stockinger et al. (1997) Proc. Natl. Acad. Sci. U.S.A. 94:1035-1040). The AP2 domain may comprise amino acids 45, 46, 48, 50-52, 54, 59, 60, 62, 64, 65, 67, 68, 71-73, 75-77, 79, 81, 83-91, 93-96, 99, 101, 102 and 104-106 of CBF1 (G40; SEQ ID NO: 2). Additionally, the CBF-related polypeptide may comprise one or more of the following peptides: PKXXAGR (amino acids 31-37 of SEQ ID NO: 2), or AGRXKF (amino acids 35-40 of SEQ ID NO: 2) or ETRHP (amino acids 42-46 of SEQ ID NO: 2).
A “regulatory region” is a region that can regulate the transcription of a gene coding sequence. The regulatory region may be a promoter or an enhancer. The regulatory region sequence is “operably linked” when it is placed into a functional relationship with the gene coding sequence. For example, a promoter or enhancer is operably linked to a gene coding sequence if the presence of the promoter or enhancer increases the level of expression of the gene coding sequence. Promoters may increase transcription of a gene at all times (constitutive promoter), increase transcription only in the presence of specific agents or events (inducible promoter), increase transcription in specific tissue(s) (tissue specific promoter) or during specific stages of cell or tissue or organism development (developmental stage specific promoter).
“Cell protectant level modification” refers to a detectable difference in cell protectant levels in a transformed cell expressing a polynucleotide or polypeptide of the present invention compared with a cell not doing so, such as a wild type cell. The trait modification may entail at least a 5% increase or decrease in an observed trait (difference), at least a 10% difference, at least a 20% difference, at least a 30%, at least a 50%, at least a 70%, at least a 100% or a greater difference. It is known that there may be a natural variation in the modified cell protectant levels. Therefore, the cell protectant level modification observed entails a change in the normal distribution of the levels in transformed cells compared with the distribution observed in wild type cells.
“Cold-acclimating a cell” and “cold acclimation” refers to a process whereby a transformed cell is exposed to temperatures below about 12° C. for different periods of time to elicit higher levels of a cell protectant compared with cell protectant levels in a cell that has not been cold acclimated.
Traits that may be Modified
Trait modifications of particular interest include those to seed (such as embryo or endosperm), fruit, root, flower, leaf, stem, shoot, seedling or the like, including: enhanced tolerance to environmental conditions including freezing, chilling, heat, drought, water saturation, radiation and ozone; improved tolerance to microbial, fungal or viral diseases; improved tolerance to pest infestations, including nematodes, mollicutes, parasitic higher plants or the like; decreased herbicide sensitivity; improved tolerance of heavy metals or enhanced ability to take up heavy metals; improved growth under poor photoconditions (e.g., low light and/or short day length), or changes in expression levels of genes of interest. Other phenotype that can be modified relate to the production of plant metabolites, such as variations in the production of taxol, tocopherol, tocotrienol, sterols, phytosterols, vitamins, wax monomers, anti-oxidants, amino acids, lignins, cellulose, tannins, prenyllipids (such as chlorophylls and carotenoids), glucosinolates, and terpenoids, enhanced or compositionally altered protein or oil production (especially in seeds), or modified sugar (insoluble or soluble) and/or starch composition. Physical plant characteristics or traits that can be modified include cell development (such as the number of trichomes), fruit and seed size and number, yields of plant parts such as stems, leaves, inflorescences, and roots, the stability of the seeds during storage, characteristics of the seed pod (e.g., susceptibility to shattering), root hair length and quantity, internode distances, or the quality of seed coat. Plant growth characteristics that can be modified include growth rate, germination rate of seeds, vigor of plants and seedlings, leaf and flower senescence, male sterility, apomixis, flowering time, flower abscission, rate of nitrogen uptake, osmotic sensitivity to soluble sugar concentrations, biomass or transpiration characteristics, as well as plant architecture characteristics such as apical dominance, branching patterns, number of organs, organ identity, organ shape or size.
Transcription Factors Modify Expression of Endogenous Genes
Expression of genes that encode transcription factors that modify expression of endogenous genes, polynucleotides, and proteins are well known in the art. In addition, transgenic plants comprising isolated polynucleotides encoding transcription factors may also modify expression of endogenous genes, polynucleotides, and proteins. Examples include Peng et al. (1997, Genes and Development 11:3194-3205) and Peng et al. (1999, Nature, 400:256-261). In addition, many others have demonstrated that an Arabidopsis transcription factor expressed in an exogenous plant species elicits the same or very similar phenotypic response. See, for example, Fu et al. (2001, Plant Cell 13:1791-1802); Nandi et al. (2000, Curr. Biol. 10:215-218); Coupland (1995, Nature 377:482-483); and Weigel and Nilsson (1995, Nature 377:482-500).
In another example, Mandel et al. (1992, Cell 71-133-143) and Suzuki et al. (2001, Plant J. 28:409-418) teach that a transcription factor expressed in another plant species elicits the same or very similar phenotypic response of the endogenous sequence, as often predicted in earlier studies of Arabidopsis transcription factors in Arabidopsis. Other examples can be found in the teachings of Müller et al. (2001, Plant J. 28:169-179); Kim et al. (2001, Plant J. 25:247-259); Kyozuka and Shimamoto (2002, Plant Cell Physiol. 43:130-135); Boss and Thomas (2002, Nature, 416:847-850); He et al. (2000, Transgenic Res., 9:223-227); and Robson et al. (2001, Plant J. 28:619-631).
In yet another example, Gilmour et al. (1998, Plant J. 16:433-442) teach an Arabidopsis AP2 transcription factor, CBF1, which, when overexpressed in transgenic plants, increases plant freezing tolerance. An alignment of the CBF proteins from Arabidopsis, B. napus, wheat, rye, and tomato revealed the presence of conserved amino acid sequences, PKK/RPAGRxKFxETRHP and DSAWR, that bracket the AP2/EREBP DNA binding domains of the proteins and distinguish them from other members of the AP2/EREBP protein family.
Polypeptides and Polynucleotides of the Invention
The present invention provides, among other things, transcription factors (TFs), and transcription factor homologue polypeptides, and isolated or recombinant polynucleotides encoding the polypeptides, or novel variant polypeptides or polynucleotides encoding novel variants of transcription factors derived from the specific sequences provided here. These polypeptides and polynucleotides may be employed to modify a plant's characteristic.
Exemplary polynucleotides encoding the polypeptides of the invention were identified in the Arabidopsis thaliana GenBank database using publicly available sequence analysis programs and parameters. Sequences initially identified were then further characterized to identify sequences comprising specified sequence strings corresponding to sequence motifs present in families of known transcription factors. In addition, further exemplary polynucleotides encoding the polypeptides of the invention were identified in the plant GenBank database using publicly available sequence analysis programs and parameters. Sequences initially identified were then further characterized to identify sequences comprising specified sequence strings corresponding to sequence motifs present in families of known transcription factors. Polynucleotide sequences meeting such criteria were confirmed as transcription factors.
Additional polynucleotides of the invention were identified by screening Arabidopsis thaliana and/or other plant cDNA libraries with probes corresponding to known transcription factors under low stringency hybridization conditions. Additional sequences, including full length coding sequences were subsequently recovered by the rapid amplification of cDNA ends (RACE) procedure, using a commercially available kit according to the manufacturer's instructions. Where necessary, multiple rounds of RACE are performed to isolate 5′ and 3′ ends. The full length cDNA was then recovered by a routine end-to-end polymerase chain reaction (PCR) using primers specific to the isolated 5′ and 3′ ends. Exemplary sequences are provided in the Sequence Listing.
The polynucleotides of the invention can be or were ectopically expressed in overexpressor or knockout plants and the changes in the characteristics or traits of the plants observed. Therefore, the polynucleotides and polypeptides can be employed to improve the characteristics or traits of plants.
The polynucleotides of the invention can be or were ectopically expressed in overexpressor plant cells and the changes in the expression levels of a number of genes, polynucleotides, and/or proteins of the plant cells observed. Therefore, the polynucleotides and polypeptides can be employed to change expression levels of a genes, polynucleotides, and/or proteins of plants.
Producing Polypeptides
The polynucleotides of the invention include sequences that encode transcription factors and transcription factor homologue polypeptides and sequences complementary thereto, as well as unique fragments of coding sequence, or sequence complementary thereto. Such polynucleotides can be, e.g., DNA or RNA, e.g., mRNA, cRNA, synthetic RNA, genomic DNA, cDNA synthetic DNA, oligonucleotides, etc. The polynucleotides are either double-stranded or single-stranded, and include either, or both sense (i.e., coding) sequences and antisense (i.e., non-coding, complementary) sequences. The polynucleotides include the coding sequence of a transcription factor, or transcription factor homologue polypeptide, in isolation, in combination with additional coding sequences (e.g., a purification tag, a localization signal, as a fusion-protein, as a pre-protein, or the like), in combination with non-coding sequences (e.g., introns or inteins, regulatory elements such as promoters, enhancers, terminators, and the like), and/or in a vector or host environment in which the polynucleotide encoding a transcription factor or transcription factor homologue polypeptide is an endogenous or exogenous gene.
A variety of methods exist for producing the polynucleotides of the invention. Procedures for identifying and isolating DNA clones are well known to those of skill in the art, and are described in, e.g., Berger and Kimmel, Guide to Molecular Cloning Techniques, Methods in Enzymology volume 152 Academic Press, Inc., San Diego, Calif. (“Berger”); Sambrook et al., Molecular Cloning—A Laboratory Manual (2nd Ed.), Vol. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 1989 (“Sambrook”) and Current Protocols in Molecular Biology, F. M. Ausubel et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (supplemented through 2000) (“Ausubel”).
Alternatively, polynucleotides of the invention, can be produced by a variety of in vitro amplification methods adapted to the present invention by appropriate selection of specific or degenerate primers. Examples of protocols sufficient to direct persons of skill through in vitro amplification methods, including the polymerase chain reaction (PCR) the ligase chain reaction (LCR), Qbeta-replicase amplification and other RNA polymerase mediated techniques (e.g., NASBA), e.g., for the production of the homologous nucleic acids of the invention are found in Berger (supra), Sambrook (supra), and Ausubel (supra), as well as Mullis et al., (1987) PCR Protocols A Guide to Methods and Applications (Innis et al. eds) Academic Press Inc. San Diego, Calif. (1990) (Innis). Improved methods for cloning in vitro amplified nucleic acids are described in Wallace et al., U.S. Pat. No. 5,426,039. Improved methods for amplifying large nucleic acids by PCR are summarized in Cheng et al. (1994) Nature 369: 684-685 and the references cited therein, in which PCR amplicons of up to 40 kb are generated. One of skill will appreciate that essentially any RNA can be converted into a double stranded DNA suitable for restriction digestion, PCR expansion and sequencing using reverse transcriptase and a polymerase. See, e.g., Ausubel, Sambrook and Berger, all supra.
Alternatively, polynucleotides and oligonucleotides of the invention can be assembled from fragments produced by solid-phase synthesis methods. Typically, fragments of up to approximately 100 bases are individually synthesized and then enzymatically or chemically ligated to produce a desired sequence, e.g., a polynucleotide encoding all or part of a transcription factor. For example, chemical synthesis using the phosphoramidite method is described, e.g., by Beaucage et al. (1981) Tetrahedron Letters 22:1859-1869; and Matthes et al. (1984) EMBO J. 3:801-805. According to such methods, oligonucleotides are synthesized, purified, annealed to their complementary strand, ligated and then optionally cloned into suitable vectors. And if so desired, the polynucleotides and polypeptides of the invention can be custom ordered from any of a number of commercial suppliers.
Homologous Sequences
Sequences homologous, i.e., that share significant sequence identity or similarity, to those provided in the Sequence Listing, derived from Arabidopsis thaliana or from other plants of choice are also an aspect of the invention. Homologous sequences can be derived from any plant including monocots and dicots and in particular agriculturally important plant species, including but not limited to, crops such as soybean, wheat, corn, potato, cotton, rice, rape, oilseed rape (including rapeseed and canola), sunflower, alfalfa, sugarcane and turf; or fruits and vegetables, such as banana, blackberry, blueberry, strawberry, and raspberry, cantaloupe, carrot, cauliflower, coffee, cucumber, eggplant, grapes, honeydew, lettuce, mango, melon, onion, papaya, peas, peppers, pineapple, pumpkin, spinach, squash, sweet corn, tobacco, tomato, watermelon, rosaceous fruits (such as apple, peach, pear, cherry and plum) and vegetable brassicas (such as broccoli, cabbage, cauliflower, Brussels sprouts, and kohlrabi). Other crops, fruits and vegetables whose phenotype can be changed include barley, rye, millet, sorghum, currant, avocado, citrus fruits such as oranges, lemons, grapefruit and tangerines, artichoke, cherries, nuts such as the walnut and peanut, endive, leek, roots, such as arrowroot, beet, cassaya, turnip, radish, yam, and sweet potato, and beans. The homologous sequences may also be derived from woody species, such pine, poplar and eucalyptus, or mint or other labiates.
Orthologs and Paralogs
Several different methods are known by those of skill in the art for identifying and defining these functionally homologous sequences. Three general methods for defining paralogs and orthologs are described; a paralog or ortholog or homolog may be identified by one or more of the methods described below.
Orthologs and paralogs are evolutionarily related genes that have similar sequence and similar functions. Orthologs are structurally related genes in different species that are derived by a speciation event. Paralogs are structurally related genes within a single species and that are derived by a duplication event.
Within a single plant species, gene duplication may cause two copies of a particular gene, giving rise to two or more genes with similar sequence and similar function known as paralogs. A paralog is therefore a similar gene with a similar function within the same species. Paralogs typically cluster together or in the same lade (a group of similar genes) when a gene family phylogeny is analyzed using programs such as CLUSTAL (Thompson et al. (1994) Nucleic Acids Res. 22:4673-4680; Higgins et al. (1996) Methods Enzymol. 266 383-402). Groups of similar genes can also be identified with pair-wise BLAST analysis (Feng and Doolittle (1987) J. Mol. Evol. 25:351-360). For example, a lade of very similar MADS domain transcription factors from Arabidopsis all share a common function in flowering time (Ratcliffe et al. (2001) Plant Physiol. 126:122-132), and a group of very similar AP2 domain transcription factors from Arabidopsis are involved in tolerance of plants to freezing (Gilmour et al. (1998) Plant J. 16:433-442). Analysis of groups of similar genes with similar function that fall within one lade can yield sub-sequences that are particular to the lade. These sub-sequences, known as consensus sequences, can not only be used to define the sequences within each lade, but define the functions of these genes; genes within a lade may contain paralogous sequences, or orthologous sequences that share the same function. (See also, for example, Mount, D. W. (2001) Bioinformatics: Sequence and Genome Analysis Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. page 543.)
Speciation, the production of new species from a parental species, can also give rise to two or more genes with similar sequence and similar function. These genes, termed orthologs, often have an identical function within their host plants and are often interchangeable between species without losing function. Because plants have common ancestors, many genes in any plant species will have a corresponding orthologous gene in another plant species. Once a phylogenic tree for a gene family of one species has been constructed using a program such as CLUSTAL (Thompson et al. (1994) Nucleic Acids Res. 22:4673-4680; Higgins et al. (1996) Methods Enzymol. 266:383-402), potential orthologous sequences can placed into the phylogenetic tree and its relationship to genes from the species of interest can be determined. Once the ortholog pair has been identified, the function of the test ortholog can be determined by determining the function of the reference ortholog.
Transcription factors that are homologous to the listed sequences will typically share at least about 30% amino acid sequence identity, or at least about 30% amino acid sequence identity outside of a known consensus sequence or consensus DNA-binding site. More closely related transcription factors can share at least about 50%, about 60%, about 65%, about 70%, about 75% or about 80% or about 90% or about 95% or about 98% or more sequence identity with the listed sequences, or with the listed sequences but excluding or outside a known consensus sequence or consensus DNA-binding site, or with the listed sequences excluding one or all conserved domain. Factors that are most closely related to the listed sequences share, e.g., at least about 85%, about 90% or about 95% or more % sequence identity to the listed sequences, or to the listed sequences but excluding or outside a known consensus sequence or consensus DNA-binding site or outside one or all conserved domain. At the nucleotide level, the sequences will typically share at least about 40% nucleotide sequence identity, preferably at least about 50%, about 60%, about 70% or about 80% sequence identity, and more preferably about 85%, about 90%, about 95% or about 97% or more sequence identity to one or more of the listed sequences, or to a listed sequence but excluding or outside a known consensus sequence or consensus DNA-binding site, or outside one or all conserved domain. The degeneracy of the genetic code enables major variations in the nucleotide sequence of a polynucleotide while maintaining the amino acid sequence of the encoded protein. Conserved domains within a transcription factor family may exhibit a higher degree of sequence homology, such as at least 65% sequence identity including conservative substitutions, and preferably at least 80% sequence identity, and more preferably at least 85%, or at least about 86%, or at least about 87%, or at least about 88%, or at least about 90%, or at least about 95%, or at least about 98% sequence identity. Transcription factors that are homologous to the listed sequences should share at least 30%, or at least about 60%, or at least about 75%, or at least about 80%, or at least about 90%, or at least about 95% amino acid sequence identity over the entire length of the polypeptide or the homolog. In addition, transcription factors that are homologous to the listed sequences should share at least 30%, or at least about 60%, or at least about 75%, or at least about 80%, or at least about 90%, or at least about 95% amino acid sequence similarity over the entire length of the polypeptide or the homolog.
Percent identity can be determined electronically, e.g., by using the MEGALIGN program (DNASTAR, Inc. Madison, Wis.). The MEGALIGN program can create alignments between two or more sequences according to different methods, e.g., the clustal method. (See, e.g., Higgins, D. G. and P. M. Sharp (1988) Gene 73:237-244.) The clustal algorithm groups sequences into clusters by examining the distances between all pairs. The clusters are aligned pairwise and then in groups. Other alignment algorithms or programs may be used, including FASTA, BLAST, or ENTREZ, FASTA and BLAST. These are available as a part of the GCG sequence analysis package (University of Wisconsin, Madison, Wis.), and can be used with or without default settings. ENTREZ is available through the National Center for Biotechnology Information. In one embodiment, the percent identity of two sequences can be determined by the GCG program with a gap weight of 1, e.g., each amino acid gap is weighted as if it were a single amino acid or nucleotide mismatch between the two sequences (see U.S. Pat. No. 6,262,333).
Other techniques for alignment are described in Methods in Enzymology, vol. 266: Computer Methods for Macromolecular Sequence Analysis (1996), ed. Doolittle, Academic Press, Inc., San Diego, Calif., USA. Preferably, an alignment program that permits gaps in the sequence is utilized to align the sequences. The Smith-Waterman is one type of algorithm that permits gaps in sequence alignments. See Methods Mol. Biol. 70: 173-187 (1997). Also, the GAP program using the Needleman and Wunsch alignment method can be utilized to align sequences. An alternative search strategy uses MPSRCH software, which runs on a MASPAR computer. MPSRCH uses a Smith-Waterman algorithm to score sequences on a massively parallel computer. This approach improves ability to pick up distantly related matches, and is especially tolerant of small gaps and nucleotide sequence errors. Nucleic acid-encoded amino acid sequences can be used to search both protein and DNA databases.
The percentage similarity between two polypeptide sequences, e.g., sequence A and sequence B, is calculated by dividing the length of sequence A, minus the number of gap residues in sequence A, minus the number of gap residues in sequence B, into the sum of the residue matches between sequence A and sequence B, times one hundred. Gaps of low or of no similarity between the two amino acid sequences are not included in determining percentage similarity. Percent identity between polynucleotide sequences can also be counted or calculated by other methods known in the art, e.g., the Jotun Hein method. (See, e.g., Hein, J. (1990) Methods Enzymol. 183:626-645.) Identity between sequences can also be determined by other methods known in the art, e.g., by varying hybridization conditions (see US Patent Application No. 20010010913).
Thus, the invention provides methods for identifying a sequence similar or paralogous or orthologous or homologous to one or more polynucleotides as noted herein, or one or more target polypeptides encoded by the polynucleotides, or otherwise noted herein and may include linking or associating a given plant phenotype or gene function with a sequence. In the methods, a sequence database is provided (locally or across an inter or intra net) and a query is made against the sequence database using the relevant sequences herein and associated plant phenotypes or gene functions.
In addition, one or more polynucleotide sequences or one or more polypeptides encoded by the polynucleotide sequences may be used to search against a BLOCKS (Bairoch et al. (1997) Nucleic Acids Res. 25:217-221), PFAM, and other databases which contain previously identified and annotated motifs, sequences and gene functions. Methods that search for primary sequence patterns with secondary structure gap penalties (Smith et al. (1992) Protein Engineering 5:35-51) as well as algorithms such as Basic Local Alignment Search Tool (BLAST; Altschul, S. F. (1993) J. Mol. Evol. 36:290-300; Altschul et al. (1990) supra), BLOCKS (Henikoff, S. and Henikoff, G. J. (1991) Nucleic Acids Research 19:6565-6572), Hidden Markov Models (HMM; Eddy, S. R. (1996) Cur. Opin. Str. Biol. 6:361-365; Sonnhammer et al. (1997) Proteins 28:405-420), and the like, can be used to manipulate and analyze polynucleotide and polypeptide sequences encoded by polynucleotides. These databases, algorithms and other methods are well known in the art and are described in Ausubel et al. (1997; Short Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., unit 7.7) and in Meyers, R. A. (1995; Molecular Biology and Biotechnology, Wiley VCH, New York N.Y., p 856-853).
Furthermore, methods using manual alignment of sequences similar or homologous to one or more polynucleotide sequences or one or more polypeptides encoded by the polynucleotide sequences may be used to identify regions of similarity and conserved domains. Such manual methods are well-known of those of skill in the art and can include, for example, comparisons of tertiary structure between a polypeptide sequence encoded by a polynucleotide which comprises a known function with a polypeptide sequence encoded by a polynucleotide sequence which has a function not yet determined. Such examples of tertiary structure may comprise predicted alpha helices, beta-sheets, amphipathic helices, leucine zipper motifs, zinc finger motifs, proline-rich regions, cysteine repeat motifs, and the like.
CBF Genes and Related Sequences
Many plants, including Arabidopsis, show increased resistance to freezing after they have been exposed to low, non-freezing temperatures. This cold-acclimation response is associated with the induction of COR (cold-regulated) genes mediated by the C-repeat/drought-responsive element (CRT/DRE) DNA regulatory element) (Baker et al. (1994) Plant. Mol. Biol. 24:701-713; Yamaguchi-Shinozaki and Shinozaki (1994) Plant Cell 6, 251-264). Increased expression of Arabidopsis CBF genes (transcriptional activators that bind to the CRT/DRE sequence), induce COR gene expression and increase the freezing tolerance of non-cold acclimated Arabidopsis plants. CBF genes are thus regulators of the cold acclimation response, and act by controlling the level of COR gene expression, which in turn promotes tolerance to freezing.
It is believed that a significant class of environmental stress tolerance regulatory genes encode for binding proteins with an AP2 domain capable of binding to a DNA regulatory sequence. Each of the presently disclosed CBF gene sequences encodes a binding protein that includes an AP2 domain, the latter being a DNA-binding motif similar to those present in Arabidopsis proteins APETALA2, AINTEGUMENTA and TINY, the tobacco ethylene response element binding proteins, and numerous other plant proteins. The AP2 domains of CBF binding proteins in general, including the CBF binding proteins described herein, share significant homology, and comprise a consensus sequence sufficiently homologous to any one of the consensus sequences shown in
CBF1 (G40; SEQ ID NO: 2), CBF2 (G41; SEQ ID NO: 13) and CBF3 (G42; SEQ ID NO: 15) have similar sequences, particularly in the AP2 domain (defined by the consensus sequence defined above and bounded by: HP-Y-GVR - - - ADS). CBF2 has 95% sequence identity with CBF1 in the AP2 domain, and CBF3 shares 96% sequence identity with CBF1 in the AP2 domain. These three and related genes can be used to prepare transgenic plants and plants with altered traits. CBF1, for example, was studied using transgenic plants in which the gene encoding the protein was expressed under the control of the 35S promoter (for a more complete discussion of studies involving CBF1, CBF2 and CBF3 experiments, see examples, below). CBF1 was shown to improve tolerance to freezing and salt stress in Arabidopsis and Canola. CBF1 could thus be used to manipulate those tolerances, and to generate plants that might germinate and survive under such adverse conditions. For example, evaporation from the soil surface causes upward water movement and salt accumulation in the upper soil layer where the seeds are placed. Thus, germination normally takes place at a salt concentration much higher than the mean salt concentration in the whole soil profile. Increased salt tolerance during the germination stage of a crop plant would impact survivability and yield. If the activity of CBF1 is regulated at a post-translational level (e.g., by being phosphorylated), it might be possible to engineer constitutively active versions of the protein that protect the plant under adverse environmental conditions.
G912 (SEQ ID NO: 97). G912 was recognized by Applicants as the AP2/EREBP gene most closely related to Arabidopsis CBF1, CBF2, and CBF3 CBF3 (SEQ ID NO: 2, 13, and 15, respectively) (Stockinger et al., 1997; Gilmour et al., 1998), G912 shares 93%, 91 and 93% sequence identity with CBF1, CBF2 and CBF3, respectively, in the AP2 domain. G912 sequence similarity with CBF1, 2 and 3 extends beyond the conserved AP2 domain. This AP2/EREBP transcription factor is also closely related to the members of the CBF-like subgroup of AP2/EREBP proteins from other plants, such as AF084185 Brassica napus dehydration responsive element binding protein. G912 was identified in the sequence of P1 clone MSG15 (GenBank accession number AB015478; gene MSG15.6; no published information is available about the functions of G912).
G912 expression appears to be induced by cold, drought, and osmotic stress. The function of G912 was studied using transgenic plants in which this gene was expressed under the control of the 35S promoter. Plants overexpressing G912 were more freezing and drought tolerant than the wild-type controls.
All these results mirror the extensive body of work presented herein that has shown that related genes CBF1, CBF2, and CBF3 are involved in the control of the low-temperature response in Arabidopsis, and that those genes can be used to improve freezing, drought, and salt tolerance in plants (Stockinger et al., 1997; Gilmour et al., 1998; Jaglo-Ottosen et al., 1998; Liu et al., 1998, Kasuga et al., 1999). In addition, G912 overexpressing plants also exhibit a sugar sensing phenotype: reduced seedling vigor and cotyledon expansion upon germination on high glucose media.
Polypeptide transcription factors from other plant species (odd numbered SEQ ID NOs: 39-95). As described in more detail in Example 13, below, a PCR strategy was used to isolate CBF homologues from a number of species of plants both related and diverse from Arabidopsis. These species included Brassica juncea, Brassica napus, Brassica oleracea, Brassica rapa, Glycine max, Raphanus sativus and Zea mays. The nucleotide (e.g. bjCBF1) and peptide sequences (e.g. BJCBF1-PEP) of these isolated CBF homologues are shown in
SEQ ID NOs: 39-45 are found in B. juncea. The AP2 regions present in each of these sequences, and which may be found as subsequences in the corresponding sequence s in the Sequence Listing, are:
Other Arabidopsis Paralogs
G2513 (SEQ ID NO: 99) G2513 is also closely related to CBF1, CBF2, and CBF3 (SEQ ID Nos: 2, 13 and 15, respectively). G2513 shares 73% sequence identity with CBF1, 73% sequence identity with CBF2, and 52%% sequence identity with CBF3. In the AP2 domain G2513 shares 77%, 75 and 80% identity with CBF1, CBF2 and CBF3, respectively.
G2513 corresponds to gene T12C24.14 (AAF88096). G2513 shows sequence similarity, outside of the conserved AP2 domain, with a protein from Nicotiana tabacum (gi12003384 AF211531—1 Avr9/Cf-9 rapidly elicited protein 111B [Nicotiana tabacum]). No published information is available about the functions of G2513. G2513-overexpressing plants were initially small with narrow dark green leaves, grew slowly and initiated floral buds several weeks later than in wild-type controls.
G2513 forms part of a monophyletic group within the Arabidopsis AP2/EREBP family that also includes G40 (SEQ ID NO: 2), G41 (SEQ ID NO: 13), G41 (SEQ ID NO: 15), and G912 (SEQ ID NO: 97), (i.e., CBF1-4).
G2513 is ubiquitously expressed, at significantly higher levels in rosette leaves, flower, and embryo tissues. Because of its phylogenetic relationship to the CBF genes and the delay in floral bud development, G2513 may be used to delay flowering and increase plant biomass relative to control after the latter flowers.
G2107 (SEQ ID NO: 101). G2107 shares 44% sequence identity with CBF1 (SEQ ID NO: 2), 45% sequence identity with CBF2 (SEQ ID NO: 13), and 51%% sequence identity with CBF3 (SEQ ID NO: 15). In the AP2 domain G2107 shares 75%, 74 and 79% sequence identity with CBF1, CBF2 and CBF3, respectively. G2107 shows sequence similarity, outside of the conserved AP2 domain, with a protein from Nicotiana tabacum(gi12003384 AF211531—1 Avr9/Cf-9 rapidly elicited protein 111B [Nicotiana tabacum]). G2107 corresponds to gene F16M19.17 (AAF18701). No published information is available about the function of G2107.
G2107 expression is detected in floral tissues (including embryo and silique), as well as in rosette leaves, but not in roots or germinating seedlings. G2106 is ubiquitously expressed, at significantly higher levels in rosette leaves, flower, and embryo tissues. Because of its phylogenetic relationship to the CBF genes and the delay in floral bud development, G2107 may be used to delay flowering and increase plant biomass relative to control after the latter flowers or when environmental conditions induce stress in control plants.
G21 (SEQ ID NO: 103). G21 corresponds to gene At2g44940 (AAD32841). G21 corresponds to gene At2g44940 (AAD32841). G2107 shares 57% sequence identity with CBF1 (SEQ ID NO: 2), 58% sequence identity with CBF2 (SEQ ID NO: 13), and 53%% sequence identity with CBF3 (SEQ ID NO: 15). In the AP2 domain G21 shares 76%, 72 and 74% sequence identity with CBF1, CBF2 and CBF3, respectively. G21 does not show extensive sequence similarity with known genes from other plant species outside of the conserved AP2/EREBP domain.
Overexpression of G21 caused alterations in plant growth and development: 35S::G21 plants were smaller than wild type, often possessed curled, darker green leaves, and showed reduced fertility. No alterations were detected in 35S::G21 plants in the physiological and biochemical analyses that were performed.
G21 is ubiquitously expressed, and appears to be induced by several environmental or physiological conditions, in particular cold and abscisic acid.
Identifying Polynucleotides or Nucleic Acids by Hybridization
Polynucleotides homologous to the sequences illustrated in the Sequence Listing and tables 4-10 can be identified, e.g., by hybridization to each other under stringent or under highly stringent conditions. Single stranded polynucleotides hybridize when they associate based on a variety of well characterized physical-chemical forces, such as hydrogen bonding, solvent exclusion, base stacking and the like. The stringency of a hybridization reflects the degree of sequence identity of the nucleic acids involved, such that the higher the stringency, the more similar are the two polynucleotide strands. Stringency is influenced by a variety of factors, including temperature, salt concentration and composition, organic and non-organic additives, solvents, etc. present in both the hybridization and wash solutions and incubations (and number thereof), as described in more detail in the references cited above.
Encompassed by the invention are polynucleotide sequences that are capable of hybridizing to the claimed transcription factor polynucleotide sequences, and, in particular, to those shown in SEQ ID Nos: 1, 12, 14, 16, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 115, 117, 119, 121, 123 and 125 and fragments thereof under various conditions of stringency. (See, e.g., Wahl, G. M. and S. L. Berger (1987) Methods Enzymol. 152:399-407; Kimmel, A. R. (1987) Methods Enzymol. 152:507-511.) Estimates of homology are provided by either DNA-DNA or DNA-RNA hybridization under conditions of stringency as is well understood by those skilled in the art (Hames and Higgins, Eds. (1985) Nucleic Acid Hybridisation, IRL Press, Oxford, U.K.). Stringency conditions can be adjusted to screen for moderately similar fragments, such as homologous sequences from distantly related organisms, to highly similar fragments, such as genes that duplicate functional enzymes from closely related organisms. Post-hybridization wash conditions determine stringency conditions.
In addition to the present nucleotide sequences listed in the Sequence Listing, full length cDNA, orthologs, paralogs and homologs of the present nucleotide sequences may be identified and isolated using well known methods. The cDNA libraries orthologs, paralogs and homologs of the present nucleotide sequences may be screened using hybridization methods to determine their utility as hybridization target or amplification probes.
An example of stringent hybridization conditions for hybridization of complementary nucleic acids which have more than 100 complementary residues on a filter in a Southern or northern blot is about 5° C. to 20° C. lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH. The Tm is the temperature (under defined ionic strength and pH) at which 50% of the target sequence hybridizes to a perfectly matched probe. Nucleic acid molecules that hybridize under stringent conditions will typically hybridize to a probe based on either the entire cDNA or selected portions, e.g., to a unique subsequence, of the cDNA under wash conditions of 0.2×SSC to 2.0×SSC, 0.1% SDS at 50-65° C. For example, high stringency is about 0.2×SSC, 0.1% SDS at 65° C. Ultra-high stringency will be the same conditions except the wash temperature is raised about 3 to about 5° C., and ultra-ultra-high stringency will be the same conditions except the wash temperature is raised about 6 to about 9° C. For identification of less closely related homologues washes can be performed at a lower temperature, e.g., 50° C. In general, stringency is increased by raising the wash temperature and/or decreasing the concentration of SSC, as known in the art.
In another example, stringent salt concentration will ordinarily be less than about 750 mM NaCl and 75 mM trisodium citrate, preferably less than about 500 mM NaCl and 50 mM trisodium citrate, and most preferably less than about 250 mM NaCl and 25 mM trisodium citrate. Low stringency hybridization can be obtained in the absence of organic solvent, e.g., formamide, while high stringency hybridization can be obtained in the presence of at least about 35% formamide, and most preferably at least about 50% formamide. Stringent temperature conditions will ordinarily include temperatures of at least about 30° C., more preferably of at least about 37° C., and most preferably of at least about 42° C. Varying additional parameters, such as hybridization time, the concentration of detergent, e.g., sodium dodecyl sulfate (SDS), and the inclusion or exclusion of carrier DNA, are well known to those skilled in the art. Various levels of stringency are accomplished by combining these various conditions as needed. In a preferred embodiment, hybridization will occur at 30° C. in 750 mM NaCl, 75 mM trisodium citrate, and 1% SDS. In a more preferred embodiment, hybridization will occur at 37° C. in 500 mM NaCl, 50 mM trisodium citrate, 1% SDS, 35% formamide, and 100 μg/ml denatured salmon sperm DNA (ssDNA). In a most preferred embodiment, hybridization will occur at 42° C. in 250 mM NaCl, 25 mM trisodium citrate, 1% SDS, 50% formamide, and 200 μg/ml ssDNA. Useful variations on these conditions will be readily apparent to those skilled in the art.
The washing steps that follow hybridization can also vary in stringency. Wash stringency conditions can be defined by salt concentration and by temperature. As above, wash stringency can be increased by decreasing salt concentration or by increasing temperature. For example, stringent salt concentration for the wash steps will preferably be less than about 30 mM NaCl and 3 mM trisodium citrate, and most preferably less than about 15 mM NaCl and 1.5 mM trisodium citrate. Stringent temperature conditions for the wash steps will ordinarily include temperature of at least about 25° C., more preferably of at least about 42° C. Another preferred set of highly stringent conditions uses two final washes in 0.1×SSC, 0.1% SDS at 65° C. The most preferred high stringency washes are of at least about 68° C. For example, in a preferred embodiment, wash steps will occur at 25° C. in 30 mM NaCl, 3 mM trisodium citrate, and 0.1% SDS. In a more preferred embodiment, wash steps will occur at 42° C. in 15 mM NaCl, 1.5 mM trisodium citrate, and 0.1% SDS. In a most preferred embodiment, the wash steps will occur at 68° C. in 15 mM NaCl, 1.5 mM trisodium citrate, and 0.1% SDS. Additional variations on these conditions will be readily apparent to those skilled in the art (see U.S. Patent Application No. 20010010913).
As another example, stringent conditions can be selected such that an oligonucleotide that is perfectly complementary to the coding oligonucleotide hybridizes to the coding oligonucleotide with at least about a 5-10× higher signal to noise ratio than the ratio for hybridization of the perfectly complementary oligonucleotide to a nucleic acid encoding a transcription factor known as of the filing date of the application. Conditions can be selected such that a higher signal to noise ratio is observed in the particular assay which is used, e.g., about 15×, 25×, 35×, 50× or more. Accordingly, the subject nucleic acid hybridizes to the unique coding oligonucleotide with at least a 2× higher signal to noise ratio as compared to hybridization of the coding oligonucleotide to a nucleic acid encoding known polypeptide. Again, higher signal to noise ratios can be selected, e.g., about 5×, 10×, 25×, 35×, 50× or more. The particular signal will depend on the label used in the relevant assay, e.g., a fluorescent label, a colorimetric label, a radioactive label, or the like.
Alternatively, transcription factor homolog polypeptides can be obtained by screening an expression library using antibodies specific for one or more transcription factors. With the provision herein of the disclosed transcription factor, and transcription factor homologue nucleic acid sequences, the encoded polypeptide(s) can be expressed and purified in a heterologous expression system (e.g., E. coli) and used to raise antibodies (monoclonal or polyclonal) specific for the polypeptide(s) in question. Antibodies can also be raised against synthetic peptides derived from transcription factor, or transcription factor homologue, amino acid sequences. Methods of raising antibodies are well known in the art and are described in Harlow and Lane (1988) Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, New York. Such antibodies can then be used to screen an expression library produced from the plant from which it is desired to clone additional transcription factor homologues, using the methods described above. The selected cDNAs can be confirmed by sequencing and enzymatic activity.
Sequence Variations
Due to the degeneracy of the genetic code, many different polynucleotides can encode identical and/or substantially similar polypeptides in addition to those sequences illustrated in the Sequence Listing. A “variant” of a transcription factor may have an amino acid sequence that is different by one or more deletions, insertions, or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent transcription factor. Thus, it will be readily appreciated by those of skill in the art, that any of a variety of polynucleotide sequences is capable of encoding the transcription factors and transcription factor homologue polypeptides of the invention. Variant nucleic acids having a sequence that differs from the sequences shown in the Sequence Listing, or complementary sequences, that encode functionally equivalent peptides (i.e., peptides having some degree of equivalent or similar biological activity) but differ in sequence from the sequence shown in the sequence listing due to degeneracy in the genetic code, are also within the scope of the invention. The variant may have “conservative” changes, wherein a substituted amino acid has similar structural or chemical properties Deliberate amino acid substitutions may thus be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues, as long as the functional or biological activity of the transcription factor is retained. For example, negatively charged amino acids may include aspartic acid and glutamic acid, positively charged amino acids may include lysine and arginine, and amino acids with uncharged polar head groups having similar hydrophilicity values may include leucine, isoleucine, and valine; glycine and alanine; asparagine and glutamine; serine and threonine; and phenylalanine and tyrosine (for more detail on conservative substitutions, see Table 2). More rarely, a variant may have “non-conservative” changes, e.g., replacement of a glycine with a tryptophan. Similar minor variations may also include amino acid deletions or insertions, or both. Guidance in determining which and how many amino acid residues may be substituted, inserted or deleted without abolishing functional or biological activity may be found using computer programs well known in the art, for example, DNASTAR software (see U.S. Pat. No. 5,840,544).
Altered polynucleotide sequences encoding polypeptides include those sequences with deletions, insertions, or substitutions of different nucleotides, resulting in a polynucleotide encoding a polypeptide with at least one functional characteristic of the instant polypeptides. Included within this definition are polymorphisms which may or may not be readily detectable using a particular oligonucleotide probe of the polynucleotide encoding the instant polypeptides, and improper or unexpected hybridization to allelic variants, with a locus other than the normal chromosomal locus for the polynucleotide sequence encoding the instant polypeptides.
Allelic variant refers to any of two or more alternative forms of a gene occupying the same chromosomal locus. Allelic variation arises naturally through mutation, and may result in phenotypic polymorphism within populations. Gene mutations can be silent (i.e., no change in the encoded polypeptide) or may encode polypeptides having altered amino acid sequence. The term allelic variant is also used herein to denote a protein encoded by an allelic variant of a gene. Splice variant refers to alternative forms of RNA transcribed from a gene. Splice variation arises naturally through use of alternative splicing sites within a transcribed RNA molecule, or less commonly between separately transcribed RNA molecules, and may result in several mRNAs transcribed from the same gene. Splice variants may encode polypeptides having altered amino acid sequence. The term splice variant is also used herein to denote a protein encoded by a splice variant of an mRNA transcribed from a gene.
Those skilled in the art would recognize that SEQ ID NO: 2, for example, represents a single transcription factor; allelic variation and alternative splicing may be expected to occur. Allelic variants of SEQ ID NO: 1 can be cloned by probing cDNA or genomic libraries from different individual organisms according to standard procedures. Allelic variants of the DNA sequence shown in SEQ ID NO:1, including those containing silent mutations and those in which mutations result in amino acid sequence changes, are within the scope of the present invention, as are proteins which are allelic variants of SEQ ID NO: 2. cDNAs generated from alternatively spliced mRNAs, which retain the properties of the transcription factor are included within the scope of the present invention, as are polypeptides encoded by such cDNAs and mRNAs. Allelic variants and splice variants of these sequences can be cloned by probing cDNA or genomic libraries from different individual organisms or tissues according to standard procedures known in the art (see U.S. Pat. No. 6,388,064).
For example, Table 1 illustrates, e.g., that the codons AGC, AGT, TCA, TCC, TCG, and TCT all encode the same amino acid: serine. Accordingly, at each position in the sequence where there is a codon encoding serine, any of the above trinucleotide sequences can be used without altering the encoded polypeptide.
Sequence alterations that do not change the amino acid sequence encoded by the polynucleotide are termed “silent” variations. With the exception of the codons ATG and TGG, encoding methionine and tryptophan, respectively, any of the possible codons for the same amino acid can be substituted by a variety of techniques, e.g., site-directed mutagenesis, available in the art. Accordingly, any and all such variations of a sequence selected from the above table are a feature of the invention.
In addition to silent variations, other conservative variations that alter one, or a few amino acids in the encoded polypeptide, can be made without altering the function of the polypeptide, these conservative variants are, likewise, a feature of the invention.
For example, substitutions, deletions and insertions introduced into the sequences provided in the Sequence Listing are also envisioned by the invention. Such sequence modifications can be engineered into a sequence by site-directed mutagenesis (Wu (ed.) Meth. Enzymol. (1993) vol. 217, Academic Press) or the other methods noted below. Amino acid substitutions are typically of single residues; insertions usually will be on the order of about from 1 to 10 amino acid residues; and deletions will range about from 1 to 30 residues. In preferred embodiments, deletions or insertions are made in adjacent pairs, e.g., a deletion of two residues or insertion of two residues. Substitutions, deletions, insertions or any combination thereof can be combined to arrive at a sequence. The mutations that are made in the polynucleotide encoding the transcription factor should not place the sequence out of reading frame and should not create complementary regions that could produce secondary mRNA structure. Preferably, the polypeptide encoded by the DNA performs the desired function.
Conservative substitutions are those in which at least one residue in the amino acid sequence has been removed and a different residue inserted in its place. Such substitutions generally are made in accordance with the Table 2 when it is desired to maintain the activity of the protein. Table 2 shows amino acids which can be substituted for an amino acid in a protein and which are typically regarded as conservative substitutions.
Similar substitutions are those in which at least one residue in the amino acid sequence has been removed and a different residue inserted in its place. Such substitutions generally are made in accordance with the Table 3 when it is desired to maintain the activity of the protein. Table 3 shows amino acids which can be substituted for an amino acid in a protein and which are typically regarded as structural and functional substitutions. For example, a residue in column 1 of Table 3 may be substituted with residue in column 2; in addition, a residue in column 2 of Table 3 may be substituted with the residue of column 1.
Substitutions that are less conservative than those in Table 2 can be selected by picking residues that differ more significantly in their effect on maintaining (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a sheet or helical conformation, (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain. The substitutions which in general are expected to produce the greatest changes in protein properties will be those in which (a) a hydrophilic residue, e.g., seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g., leucyl, isoleucyl, phenylalanyl, valyl or alanyl; (b) a cysteine or proline is substituted for (or by) any other residue; (c) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histidyl, is substituted for (or by) an electronegative residue, e.g., glutamyl or aspartyl; or (d) a residue having a bulky side chain, e.g., phenylalanine, is substituted for (or by) one not having a side chain, e.g., glycine.
Further Modifying Sequences of the Invention—Mutation/Forced Evolution
In addition to generating silent or conservative substitutions as noted, above, the present invention optionally includes methods of modifying the sequences of the Sequence Listing. In the methods, nucleic acid or protein modification methods are used to alter the given sequences to produce new sequences and/or to chemically or enzymatically modify given sequences to change the properties of the nucleic acids or proteins.
Thus, in one embodiment, given nucleic acid sequences are modified, e.g., according to standard mutagenesis or artificial evolution methods to produce modified sequences. The modified sequences may be created using purified natural polynucleotides isolated from any organism or may be synthesized from purified compositions and chemicals using chemical means well know to those of skill in the art. For example, Ausubel, supra, provides additional details on mutagenesis methods. Artificial forced evolution methods are described, for example, by Stemmer (1994) Nature 370:389-391, Stemmer (1994) Proc Natl. Acad. Sci. USA 91:10747-10751, and U.S. Pat. Nos. 5,811,238, 5,837,500, and 6,242,568. Methods for engineering synthetic transcription factors and other polypeptides are described, for example, by Zhang et al. (2000) J. Biol. Chem. 275:33850-33860, Liu et al. (2001) J. Biol. Chem. 276:11323-11334, and Isalan et al. (2001) Nature Biotechnol. 19:656-660. Many other mutation and evolution methods are also available and expected to be within the skill of the practitioner.
Similarly, chemical or enzymatic alteration of expressed nucleic acids and polypeptides can be performed by standard methods. For example, sequence can be modified by addition of lipids, sugars, peptides, organic or inorganic compounds, by the inclusion of modified nucleotides or amino acids, or the like. For example, protein modification techniques are illustrated in Ausubel, supra. Further details on chemical and enzymatic modifications can be found herein. These modification methods can be used to modify any given sequence, or to modify any sequence produced by the various mutation and artificial evolution modification methods noted herein.
Accordingly, the invention provides for modification of any given nucleic acid by mutation, evolution, chemical or enzymatic modification, or other available methods, as well as for the products produced by practicing such methods, e.g., using the sequences herein as a starting substrate for the various modification approaches.
For example, optimized coding sequence containing codons preferred by a particular prokaryotic or eukaryotic host can be used e.g., to increase the rate of translation or to produce recombinant RNA transcripts having desirable properties, such as a longer half-life, as compared with transcripts produced using a non-optimized sequence. Translation stop codons can also be modified to reflect host preference. For example, preferred stop codons for Saccharomyces cerevisiae and mammals are TAA and TGA, respectively. The preferred stop codon for monocotyledonous plants is TGA, whereas insects and E. coli prefer to use TAA as the stop codon.
The polynucleotide sequences of the present invention can also be engineered in order to alter a coding sequence for a variety of reasons, including but not limited to, alterations which modify the sequence to facilitate cloning, processing and/or expression of the gene product. For example, alterations are optionally introduced using techniques which are well known in the art, e.g., site-directed mutagenesis, to insert new restriction sites, to alter glycosylation patterns, to change codon preference, to introduce splice sites, etc.
Furthermore, a fragment or domain derived from any of the polypeptides of the invention can be combined with domains derived from other transcription factors or synthetic domains to modify the biological activity of a transcription factor. For instance, a DNA-binding domain derived from a transcription factor of the invention can be combined with the activation domain of another transcription factor or with a synthetic activation domain. A transcription activation domain assists in initiating transcription from a DNA-binding site. Examples include the transcription activation region of VP16 or GAL4 (Moore et al. (1998) Proc. Natl. Acad. Sci. USA 95: 376-381; and Aoyama et al. (1995) Plant Cell 7:1773-1785), peptides derived from bacterial sequences (Ma and Ptashne (1987) Cell 51; 113-119) and synthetic peptides (Giniger and Ptashne, (1987) Nature 330:670-672).
Expression and Modification of Polypeptides
Typically, polynucleotide sequences of the invention are incorporated into recombinant DNA (or RNA) molecules that direct expression of polypeptides of the invention in appropriate host cells, transgenic plants, in vitro translation systems, or the like. Due to the inherent degeneracy of the genetic code, nucleic acid sequences which encode substantially the same or a functionally equivalent amino acid sequence can be substituted for any listed sequence to provide for cloning and expressing the relevant homologue.
Vectors, Promoters, and Expression Systems
The present invention includes recombinant constructs comprising one or more of the nucleic acid sequences herein. The constructs typically comprise a vector, such as a plasmid, a cosmid, a phage, a virus (e.g., a plant virus), a bacterial artificial chromosome (BAC), a yeast artificial chromosome (YAC), or the like, into which a nucleic acid sequence of the invention has been inserted, in a forward or reverse orientation. In a preferred aspect of this embodiment, the construct further comprises regulatory sequences, including, for example, a promoter, operably linked to the sequence. Large numbers of suitable vectors and promoters are known to those of skill in the art, and are commercially available.
General texts that describe molecular biological techniques useful herein, including the use and production of vectors, promoters and many other relevant topics, include Berger, Sambrook and Ausubel, supra. Any of the identified sequences can be incorporated into a cassette or vector, e.g., for expression in plants. A number of expression vectors suitable for stable transformation of plant cells or for the establishment of transgenic plants have been described including those described in Weissbach and Weissbach, (1989) Methods for Plant Molecular Biology, Academic Press, and Gelvin et al., (1990) Plant Molecular Biology Manual, Kluwer Academic Publishers. Specific examples include those derived from a Ti plasmid of Agrobacterium tumefaciens, as well as those disclosed by Herrera-Estrella et al. (1983) Nature 303: 209, Bevan (1984) Nucl Acid Res. 12: 8711-8721, Klee (1985) Bio/Technology 3: 637-642, for dicotyledonous plants.
Alternatively, non-Ti vectors can be used to transfer the DNA into monocotyledonous plants and cells by using free DNA delivery techniques. Such methods can involve, for example, the use of liposomes, electroporation, microprojectile bombardment, silicon carbide whiskers, and viruses. By using these methods transgenic plants such as wheat, rice (Christou (1991) Bio/Technology 9: 957-962) and corn (Gordon-Kamm (1990) Plant Cell 2: 603-618) can be produced. An immature embryo can also be a good target tissue for monocots for direct DNA delivery techniques by using the particle gun (Weeks et al. (1993) Plant Physiol 102: 1077-1084; Vasil (1993) Bio/Technology 10: 667-674; Wan and Lemeaux (1994) Plant Physiol 104: 37-48, and for Agrobacterium-mediated DNA transfer (Ishida et al. (1996) Nature Biotech 14: 745-750).
Typically, plant transformation vectors include one or more cloned plant coding sequence (genomic or cDNA) under the transcriptional control of 5′ and 3′ regulatory sequences and a dominant selectable marker. Such plant transformation vectors typically also contain a promoter (e.g., a regulatory region controlling inducible or constitutive, environmentally-or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, an RNA processing signal (such as intron splice sites), a transcription termination site, and/or a polyadenylation signal.
Examples of constitutive plant promoters which can be useful for expressing the TF sequence include: the cauliflower mosaic virus (CaMV) 35S promoter, which confers constitutive, high-level expression in most plant tissues (see, e.g., Odell et al. (1985) Nature 313:810-812); the nopaline synthase promoter (An et al. (1988) Plant Physiol 88:547-552); and the octopine synthase promoter (Fromm et al. (1989) Plant Cell 1: 977-984).
A variety of plant gene promoters that regulate gene expression in response to environmental, hormonal, chemical, developmental signals, and in a tissue-active manner can be used for expression of a TF sequence in plants. Choice of a promoter is based largely on the phenotype of interest and is determined by such factors as tissue (e.g., seed, fruit, root, pollen, vascular tissue, flower, carpel, etc.), inducibility (e.g., in response to wounding, heat, cold, drought, light, pathogens, etc.), timing, developmental stage, and the like. Numerous known promoters have been characterized and can favorably be employed to promote expression of a polynucleotide of the invention in a transgenic plant or cell of interest. For example, tissue specific promoters include: seed-specific promoters (such as the napin, phaseolin or DC3 promoter described in U.S. Pat. No. 5,773,697), fruit-specific promoters that are active during fruit ripening (such as the dru 1 promoter (U.S. Pat. No. 5,783,393), or the 2A11 promoter (U.S. Pat. No. 4,943,674) and the tomato polygalacturonase promoter (Bird et al. (1988) Plant Mol Biol 11:651-662), root-specific promoters, such as those disclosed in U.S. Pat. Nos. 5,618,988, 5,837,848 and 5,905,186, pollen-active promoters such as PTA29, PTA26 and PTA13 (U.S. Pat. No. 5,792,929), promoters active in vascular tissue (Ringli and Keller (1998) Plant Mol Biol 37:977-988), flower-specific (Kaiser et al, (1995) Plant Mol Biol 28:231-243), pollen (Baerson et al. (1994) Plant Mol Biol 26:1947-1959), carpels (Ohl et al. (1990) Plant Cell 2:837-848), pollen and ovules (Baerson et al. (1993) Plant Mol Biol 22:255-267), auxin-inducible promoters (such as that described in van der Kop et al. (1999) Plant Mol Biol 39:979-990 or Baumann et al. (1999) Plant Cell 11:323-334), cytokinin-inducible promoter (Guevara-Garcia (1998) Plant Mol Biol 38:743-753), promoters responsive to gibberellin (Shi et al. (1998) Plant Mol Biol 38:1053-1060, Willmott et al. (1998) 38:817-825) and the like. Additional promoters are those that elicit expression in response to heat (Ainley et al. (1993) Plant Mol Biol 22: 13-23), light (e.g., the pea rbcS-3A promoter, Kuhlemeier et al. (1989) Plant Cell 1:471, and the maize rbcS promoter, Schaffner and Sheen (1991) Plant Cell 3: 997); wounding (e.g., wunl, Siebertz et al. (1989) Plant Cell 1: 961); pathogens (such as the PR-1 promoter described in Buchel et al. (1999) Plant Mol. Biol. 40:387-396, and the PDF1.2 promoter described in Manners et al. (1998) Plant Mol. Biol. 38:1071-1080), and chemicals such as methyl jasmonate or salicylic acid (Gatz et al. (1997) Ann Rev Plant Physiol Plant Mol Biol 48: 89-108). In addition, the timing of the expression can be controlled by using promoters such as those acting at senescence (Gan and Amasino (1995) Science 270: 1986-1988); or late seed development (Odell et al. (1994) Plant Physiol 106:447458).
Plant expression vectors can also include RNA processing signals that can be positioned within, upstream or downstream of the coding sequence. In addition, the expression vectors can include additional regulatory sequences from the 3′-untranslated region of plant genes, e.g., a 3′ terminator region to increase mRNA stability of the mRNA, such as the PI-II terminator region of potato or the octopine or nopaline synthase 3′ terminator regions.
Additional Expression Elements
Specific initiation signals can aid in efficient translation of coding sequences. These signals can include, e.g., the ATG initiation codon and adjacent sequences. In cases where a coding sequence, its initiation codon and upstream sequences are inserted into the appropriate expression vector, no additional translational control signals may be needed. However, in cases where only coding sequence (e.g., a mature protein coding sequence), or a portion thereof, is inserted, exogenous transcriptional control signals including the ATG initiation codon can be separately provided. The initiation codon is provided in the correct reading frame to facilitate transcription. Exogenous transcriptional elements and initiation codons can be of various origins, both natural and synthetic. The efficiency of expression can be enhanced by the inclusion of enhancers appropriate to the cell system in use.
Expression Hosts
The present invention also relates to host cells which are transduced with vectors of the invention, and the production of polypeptides of the invention (including fragments thereof) by recombinant techniques. Host cells are genetically engineered (i.e., nucleic acids are introduced, e.g., transduced, transformed or transfected) with the vectors of this invention, which may be, for example, a cloning vector or an expression vector comprising the relevant nucleic acids herein. The vector is optionally a plasmid, a viral particle, a phage, a naked nucleic acid, etc. The engineered host cells can be cultured in conventional nutrient media modified as appropriate for activating promoters, selecting transformants, or amplifying the relevant gene. The culture conditions, such as temperature, pH and the like, are those previously used with the host cell selected for expression, and will be apparent to those skilled in the art and in the references cited herein, including, Sambrook and Ausubel.
The host cell can be a eukaryotic cell, such as a yeast cell, or a plant cell, or the host cell can be a prokaryotic cell, such as a bacterial cell. Plant protoplasts are also suitable for some applications. For example, the DNA fragments are introduced into plant tissues, cultured plant cells or plant protoplasts by standard methods including electroporation (Fromm et al., (1985) Proc. Natl. Acad. Sci. USA 82, 5824, infection by viral vectors such as cauliflower mosaic virus (CaMV) (Hohn et al., (1982) Molecular Biology of Plant Tumors, (Academic Press, New York) pp. 549-560; U.S. Pat. No. 4,407,956), high velocity ballistic penetration by small particles with the nucleic acid either within the matrix of small beads or particles, or on the surface (Klein et al., (1987) Nature 327, 70-73), use of pollen as vector (WO 85/01856), or use of Agrobacterium tumefaciens or A. rhizogenes carrying a T-DNA plasmid in which DNA fragments are cloned. The T-DNA plasmid is transmitted to plant cells upon infection by Agrobacterium tumefaciens, and a portion is stably integrated into the plant genome (Horsch et al. (1984) Science 233:496-498; Fraley et al. (1983) Proc. Natl. Acad. Sci. USA 80, 4803).
The cell can include a nucleic acid of the invention that encodes a polypeptide, wherein the cell expresses a polypeptide of the invention. The cell can also include vector sequences, or the like. Furthermore, cells and transgenic plants that include any polypeptide or nucleic acid above or throughout this specification, e.g., produced by transduction of a vector of the invention, are an additional feature of the invention.
Modified Amino Acid Residues
Polypeptides of the invention may contain one or more modified amino acid residues. The presence of modified amino acids may be advantageous in, for example, increasing polypeptide half-life, reducing polypeptide antigenicity or toxicity, increasing polypeptide storage stability, or the like. Amino acid residue(s) are modified, for example, co-translationally or post-translationally during recombinant production or modified by synthetic or chemical means.
Non-limiting examples of a modified amino acid residue include incorporation or other use of acetylated amino acids, glycosylated amino acids, sulfated amino acids, prenylated (e.g., farnesylated, geranylgeranylated) amino acids, PEG modified (e.g., “PEGylated”) amino acids, biotinylated amino acids, carboxylated amino acids, phosphorylated amino acids, etc. References adequate to guide one of skill in the modification of amino acid residues are replete throughout the literature.
The modified amino acid residues may prevent or increase affinity of the polypeptide for another molecule, including, but not limited to, polynucleotide, proteins, carbohydrates, lipids and lipid derivatives, and other organic or synthetic compounds.
Identification of Additional Factors
A transcription factor provided by the present invention can also be used to identify additional endogenous or exogenous molecules that can affect a phentoype or trait of interest. On the one hand, such molecules include organic (small or large molecules) and/or inorganic compounds that affect expression of (i.e., regulate) a particular transcription factor. Alternatively, such molecules include endogenous molecules that are acted upon either at a transcriptional level by a transcription factor of the invention to modify a phenotype as desired. For example, the transcription factors can be employed to identify one or more downstream gene with which is subject to a regulatory effect of the transcription factor. In one approach, a transcription factor or transcription factor homologue of the invention is expressed in a host cell, e.g., a transgenic plant cell, tissue or explant, and expression products, either RNA or protein, of likely or random targets are monitored, e.g., by hybridization to a microarray of nucleic acid probes corresponding to genes expressed in a tissue or cell type of interest, by two-dimensional gel electrophoresis of protein products, or by any other method known in the art for assessing expression of gene products at the level of RNA or protein. Alternatively, a transcription factor of the invention can be used to identify promoter sequences (i.e., binding sites) involved in the regulation of a downstream target. After identifying a promoter sequence, interactions between the transcription factor and the promoter sequence can be modified by changing specific nucleotides in the promoter sequence or specific amino acids in the transcription factor that interact with the promoter sequence to alter a plant trait. Typically, transcription factor DNA-binding sites are identified by gel shift assays. After identifying the promoter regions, the promoter region sequences can be employed in double-stranded DNA arrays to identify molecules that affect the interactions of the transcription factors with their promoters (Bulyk et al. (1999) Nature Biotechnology 17:573-577).
The identified transcription factors are also useful to identify proteins that modify the activity of the transcription factor. Such modification can occur by covalent modification, such as by phosphorylation, or by protein-protein (homo- or heteropolymer) interactions. Any method suitable for detecting protein-protein interactions can be employed. Among the methods that can be employed are co-immunoprecipitation, cross-linking and co-purification through gradients or chromatographic columns, and the two-hybrid yeast system.
The two-hybrid system detects protein interactions in vivo and is described in Chien et al. ((1991), Proc. Natl. Acad. Sci. USA 88:9578-9582) and is commercially available from Clontech (Palo Alto, Calif.). In such a system, plasmids are constructed that encode two hybrid proteins: one consists of the DNA-binding domain of a transcription activator protein fused to the TF polypeptide and the other consists of the transcription activator protein's activation domain fused to an unknown protein that is encoded by a cDNA that has been recombined into the plasmid as part of a cDNA library. The DNA-binding domain fusion plasmid and the cDNA library are transformed into a strain of the yeast Saccharomyces cerevisiae that contains a reporter gene (e.g., lacZ) whose regulatory region contains the transcription activator's binding site. Either hybrid protein alone cannot activate transcription of the reporter gene. Interaction of the two hybrid proteins reconstitutes the functional activator protein and results in expression of the reporter gene, which is detected by an assay for the reporter gene product. Then, the library plasmids responsible for reporter gene expression are isolated and sequenced to identify the proteins encoded by the library plasmids. After identifying proteins that interact with the transcription factors, assays for compounds that interfere with the TF protein-protein interactions can be preformed.
Identification of Modulators
In addition to the intracellular molecules described above, extracellular molecules that alter activity or expression of a transcription factor, either directly or indirectly, can be identified. For example, the methods can entail first placing a candidate molecule in contact with a plant or plant cell. The molecule can be introduced by topical administration, such as spraying or soaking of a plant, and then the molecule's effect on the expression or activity of the TF polypeptide or the expression of the polynucleotide monitored. Changes in the expression of the TF polypeptide can be monitored by use of polyclonal or monoclonal antibodies, gel electrophoresis or the like. Changes in the expression of the corresponding polynucleotide sequence can be detected by use of microarrays, Northerns, quantitative PCR, or any other technique for monitoring changes in mRNA expression. These techniques are exemplified in Ausubel et al. (eds) Current Protocols in Molecular Biology, John Wiley & Sons (1998, and supplements through 2001). Such changes in the expression levels can be correlated with modified plant traits and thus identified molecules can be useful for soaking or spraying on fruit, vegetable and grain crops to modify traits in plants.
Essentially any available composition can be tested for modulatory activity of expression or activity of any nucleic acid or polypeptide herein. Thus, available libraries of compounds such as chemicals, polypeptides, nucleic acids and the like can be tested for modulatory activity. Often, potential modulator compounds can be dissolved in aqueous or organic (e.g., DMSO-based) solutions for easy delivery to the cell or plant of interest in which the activity of the modulator is to be tested. Optionally, the assays are designed to screen large modulator composition libraries by automating the assay steps and providing compounds from any convenient source to assays, which are typically run in parallel (e.g., in microtiter formats on microtiter plates in robotic assays).
In one embodiment, high throughput screening methods involve providing a combinatorial library containing a large number of potential compounds (potential modulator compounds). Such “combinatorial chemical libraries” are then screened in one or more assays, as described herein, to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. The compounds thus identified can serve as target compounds.
A combinatorial chemical library can be, e.g., a collection of diverse chemical compounds generated by chemical synthesis or biological synthesis. For example, a combinatorial chemical library such as a polypeptide library is formed by combining a set of chemical building blocks (e.g., in one example, amino acids) in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound of a set length). Exemplary libraries include peptide libraries, nucleic acid libraries, antibody libraries (see, e.g., Vaughn et al. (1996) Nature Biotechnology, 14(3):309-314 and PCT/US96/10287), carbohydrate libraries (see, e.g., Liang et al. Science (1996) 274:1520-1522 and U.S. Pat. No. 5,593,853), peptide nucleic acid libraries (see, e.g., U.S. Pat. No. 5,539,083), and small organic molecule libraries (see, e.g., benzodiazepines, Baum C&EN January 18, page 33 (1993); isoprenoids, U.S. Pat. No. 5,569,588; thiazolidinones and metathiazanones, U.S. Pat. No. 5,549,974; pyrrolidines, U.S. Pat. Nos. 5,525,735 and 5,519,134; morpholino compounds, U.S. Pat. No. 5,506,337) and the like.
Preparation and screening of combinatorial or other libraries is well known to those of skill in the art. Such combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Pat. No. 5,010,175; Furka, (1991) Int. J. Pept. Prot. Res. 37:487-493; and Houghton et al. (1991) Nature 354:84-88). Other chemistries for generating chemical diversity libraries can also be used.
In addition, as noted, compound screening equipment for high-throughput screening is generally available, e.g., using any of a number of well known robotic systems that have also been developed for solution phase chemistries useful in assay systems. These systems include automated workstations including an automated synthesis apparatus and robotic systems utilizing robotic arms. Any of the above devices are suitable for use with the present invention, e.g., for high-throughput screening of potential modulators. The nature and implementation of modifications to these devices (if any) so that they can operate as discussed herein will be apparent to persons skilled in the relevant art.
Indeed, entire high throughput screening systems are commercially available. These systems typically automate entire procedures including all sample and reagent pipetting, liquid dispensing, timed incubations, and final readings of the microplate in detector(s) appropriate for the assay. These configurable systems provide high throughput and rapid start up as well as a high degree of flexibility and customization. Similarly, microfluidic implementations of screening are also commercially available.
The manufacturers of such systems provide detailed protocols the various high throughput. Thus, for example, Zymark Corp. provides technical bulletins describing screening systems for detecting the modulation of gene transcription, ligand binding, and the like. The integrated systems herein, in addition to providing for sequence alignment and, optionally, synthesis of relevant nucleic acids, can include such screening apparatus to identify modulators that have an effect on one or more polynucleotides or polypeptides according to the present invention.
In some assays it is desirable to have positive controls to ensure that the components of the assays are working properly. At least two types of positive controls are appropriate. That is, known transcriptional activators or inhibitors can be incubated with cells/plants/etc. in one sample of the assay, and the resulting increase/decrease in transcription can be detected by measuring the resulting increase in RNA/protein expression, etc., according to the methods herein. It will be appreciated that modulators can also be combined with transcriptional activators or inhibitors to find modulators that inhibit transcriptional activation or transcriptional repression. Either expression of the nucleic acids and proteins herein or any additional nucleic acids or proteins activated by the nucleic acids or proteins herein, or both, can be monitored.
In an embodiment, the invention provides a method for identifying compositions that modulate the activity or expression of a polynucleotide or polypeptide of the invention. For example, a test compound, whether a small or large molecule, is placed in contact with a cell, plant (or plant tissue or explant), or composition comprising the polynucleotide or polypeptide of interest and a resulting effect on the cell, plant, (or tissue or explant) or composition is evaluated by monitoring, either directly or indirectly, one or more of: expression level of the polynucleotide or polypeptide, activity (or modulation of the activity) of the polynucleotide or polypeptide. In some cases, an alteration in a plant phenotype can be detected following contact of a plant (or plant cell, or tissue or explant) with the putative modulator, e.g., by modulation of expression or activity of a polynucleotide or polypeptide of the invention. Modulation of expression or activity of a polynucleotide or polypeptide of the invention may also be caused by molecular elements in a signal transduction second messenger pathway and such modulation can affect similar elements in the same or another signal transduction second messenger pathway.
Subsequences
Also contemplated are uses of polynucleotides, also referred to herein as oligonucleotides, typically having at least 12 bases, preferably at least 15, more preferably at least 20, 30, or 50 bases, which hybridize under at least highly stringent (or ultra-high stringent or ultra-ultra-high stringent conditions) conditions to a polynucleotide sequence described above. The polynucleotides may be used as probes, primers, sense and antisense agents, and the like, according to methods as noted supra.
Subsequences of the polynucleotides of the invention, including polynucleotide fragments and oligonucleotides are useful as nucleic acid probes and primers. An oligonucleotide suitable for use as a probe or primer is at least about 15 nucleotides in length, more often at least about 18 nucleotides, often at least about 21 nucleotides, frequently at least about 30 nucleotides, or about 40 nucleotides, or more in length. A nucleic acid probe is useful in hybridization protocols, e.g., to identify additional polypeptide homologues of the invention, including protocols for microarray experiments. Primers can be annealed to a complementary target DNA strand by nucleic acid hybridization to form a hybrid between the primer and the target DNA strand, and then extended along the target DNA strand by a DNA polymerase enzyme. Primer pairs can be used for amplification of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR) or other nucleic-acid amplification methods. See Sambrook and Ausubel, supra.
In addition, the invention includes an isolated or recombinant polypeptide including a subsequence of at least about 15 contiguous amino acids encoded by the recombinant or isolated polynucleotides of the invention. For example, such polypeptides, or domains or fragments thereof, can be used as immunogens, e.g., to produce antibodies specific for the polypeptide sequence, or as probes for detecting a sequence of interest. A subsequence can range in size from about 15 amino acids in length up to and including the full length of the polypeptide.
To be encompassed by the present invention, an expressed polypeptide which comprises such a polypeptide subsequence performs at least one biological function of the intact polypeptide in substantially the same manner, or to a similar extent, as does the intact polypeptide. For example, a polypeptide fragment can comprise a recognizable structural motif or functional domain such as a DNA binding domain that binds to a specific DNA promoter region, an activation domain or a domain for protein-protein interactions.
2. Description of the Invention
The present invention relates to a method for increasing the levels of a cell protectant in a cell. By increasing the levels of the cell protectant, a cell's response to a variety of environmental stresses can be improved. The type of environmental stress that can be modified includes the cold or freezing tolerance of the cell or the drought or salinity tolerance of the cell. The cell protectant may be a cryoprotectant, an osmoprotectant or the like. Exemplary cell protectants include proline, sugars, lipids or the like. The method can also be used to increase levels of a number of cell protectants simultaneously.
The method entails generating a transformed cell that overexpresses a recombinant polynucleotide encoding a CBF-related polypeptide. The transformed cell may be generated by transforming a cell with an expression vector comprising a polynucleotide sequence encoding a cold-regulatable polypeptide or by breeding after the initial transformation of a parental cell comprising the expression vector. Transformed cells are then selected for cells expressing the polynucleotide and grown. The resulting cells produce higher levels of cell protectants. Higher levels of cell protectants can be detected either in the absence of or after exposure to cold temperatures (cold acclimation). However, higher levels of cell protectants are typically observed in cells that have been cold acclimated compared with levels observed in cells that have not been cold acclimated.
By increasing the levels of a single cell protectant or a combination of cell protectants simultaneously in the cell, the cell's tolerance to environmental stresses can be substantially improved, as measured for example by a plant's survival rate after exposure to freezing temperatures or the growth of a plant's roots after exposure to drought conditions or high salinity.
The present invention also relates to a method for producing a cell protectant from a cell. The method entails generating a transformed cell that overexpresses a recombinant polynucleotide encoding a CBF-related polypeptide. Expression of the recombinant polynucleotide causes metabolic pathways that produce or accumulate certain cell protectants to be turned on so that higher levels of the cell protectants are produced. For example, we have observed that the key proline biosynthetic pathway enzyme, P5CS, is expressed at higher levels when the CBF-related polynucleotide is overexpressed. Then the cell protectant, such as proline, sugars or lipids, can be isolated from the plant using well known isolation and purification methods.
The present invention can be applied to increase cell protectant levels in or improve the environmental stress tolerance of a variety of cells, in particular plant cells including monocots, dicots and gymnosperms. In particular the invention may be used for modifying the environmental stress response of agriculturally important plant species, including but not limited to, crops such as soybean, wheat, corn, potato, cotton, rice, oilseed rape (including canola), sunflower, alfalfa, sugarcane and turf; or fruits and vegetables, such as banana, blackberry, blueberry, strawberry, and raspberry, cantaloupe, carrot, cauliflower, coffee, cucumber, eggplant, grapes, honeydew, lettuce, mango, melon, onion, papaya, peas, peppers, pineapple, spinach, squash, sweet corn, tobacco, tomato, watermelon, rosaceous fruits (such as apple, peach, pear, cherry and plum) and vegetable brassicas (such as broccoli, cabbage, cauliflower, Brussels sprouts and kohlrabi). Other crops, fruits and vegetables whose phenotype may be changed include barley, currant, avocado, citrus fruits such as oranges, lemons, grapefruit and tangerines, artichoke, cherries, nuts such as the walnut and peanut, endive, leek, roots, such as arrowroot, beet, cassaya, turnip, radish, yam, sweet potato and beans. The present invention may also be employed to increase cell protectant levels in woody plants, such pine, poplar and eucalyptus.
A. CBF-Related Polypeptide
The CBF-related protein may comprise a whole gene coding sequence or a fragment or domain of a coding sequence. A “fragment or domain”, as referred to polypeptides, may be a portion of a polypeptide which performs at least one biological function of the intact polypeptide in substantially the same manner or to a similar extent as does the intact polypeptide. A fragment may comprise, for example, a DNA binding domain that binds to a specific DNA promoter region (such as the AP2 domain), an activation domain or a domain for protein-protein interactions. Fragments may vary in size from as few as 6 amino acids to the length of the intact polypeptide, but are preferably at least 30 amino acids in length and more preferably at least 60 amino acids in length. For example, one can identify any number of 60 amino acid long fragments (1-60, 5-65, 10-70, 15-75, etc.) along the length of the CBF3 polypeptide shown in
The CBF-related polypeptides encompass naturally occurring sequences. Numerous CBF-related proteins have been previously identified and include the genes, CBF1, CBF2 and CBF3 (also known as DREB1b, DREB1c and DREB1a, respectively), which are located in tandem on chromosome 4 in Arabidopsis (Gilmour et al. (1998) Plant J. 16, 433-442; Shinwari et al. (1998) Biochem. Biophys. Res. Commun. 250, 161-170). Additional examples of CBF-related polypeptides include those described in Stockinger et al. PCT publication WO99/38977, and U.S. patent application Ser. No. 09/198,119, entitled “Plant Having Altered Environmental Stress Tolerance”, filed Nov. 23, 1998 and U.S. Provisional Patent Application No. 60/165,860 entitled “Method for Modifying the Cold Resistance of Plants”, filed Nov. 16, 1999.
The CBF-related polypeptides may also encompass non-naturally occurring sequences that are derivatives of the naturally-occurring CBFs described above. For example, a non-naturally occurring sequence using domains of other transcription factors described above fused in frame, but not necessarily adjacent, with functional domains derived from other sequences or sources. Additionally, the invention includes polypeptides derived from shuffling regions of transcription factors described above by methods described in Minshull and Stemmer, U.S. Pat. No. 5,837,458, entitled “Methods and Compositions for Cellular and Metabolic Engineering” and Stemmer and Crameri, U.S. Pat. No. 5,811,238, entitled “Methods for Generating Polynucleotides having Desired Characteristics by Iterative Selection and Recombination”.
Substitutions, deletions and insertions introduced into CBF-related polypeptides are also envisioned by the invention. Such sequence modifications can be engineered into a sequence by site-directed mutagenesis (Wu (ed.) Meth. Enzymol. (1993) vol. 217, Academic Press). Amino acid substitutions are typically of single residues and may be conservative (such as serine to threonine) or non-conservative (such as lysine to glutamic acid); insertions usually will be on the order of about from 1 to 10 amino acid residues; and deletions will range about from 1 to 30 residues. In preferred embodiments, deletions or insertions are made in adjacent pairs, e.g., a deletion of two residues or insertion of two residues. Substitutions, deletions, insertions or any combination thereof may be combined to arrive at a sequence.
Additionally, the CBF-related polypeptide may encompass a polypeptide sequence that is modified by chemical or enzymatic means. The homologous sequence may be a sequence modified by lipids, sugars, peptides, organic or inorganic compounds, by the use of modified amino acids or the like. Protein modification techniques are illustrated in Ausubel et al. (eds.) Current Protocols in Molecular Biology, John Wiley & Sons (1998).
B. Altered Expression of CBF-Related Polypeptide
Any of the identified sequences may be incorporated into a cassette or vector for expression in cells, in particular plant cells. A number of expression vectors suitable for stable transformation of plant cells or for the establishment of transgenic plants have been described including those described in Weissbach and Weissbach, (1989) Methods for Plant Molecular Biology, Academic Press, and Gelvin et al., (1990) Plant Molecular Biology Manual, Kluwer Academic Publishers. Specific examples include those derived from a Ti plasmid of Agrobacterium tumefaciens, as well as those disclosed by Herrera-Estrella, L., et al., (1983) Nature 303: 209, Bevan, M., Nucl. Acids Res. (1984) 12: 8711-8721, Klee, H. J., (1985) Bio/Technology 3: 637-642. Ti-derived plasmids can be transferred into both monocot and dicot species using Agrobacterium-mediated transformation (Ishida et al (1996) Nat. Biotechnol. 14:745-50; Barton et al. (1983) Cell 32:1033-1043).
Alternatively, non-Ti vectors can be used to transfer the DNA into plant cells by using free DNA delivery techniques. Such methods may involve, for example, the use of liposomes, electroporation, microprojectile bombardment, silicon carbide whiskers, and viruses. By using these methods transgenic plants such as wheat, rice (Christou, P., (1991) Bio/Technology 9: 957-962) and corn (Gordon-Kamm, W., (1990) Plant Cell 2: 603-618) can be produced. An immature embryo can also be a good target tissue for plants for direct DNA delivery techniques by using the particle gun (Weeks, T. et al., (1993) Plant Physiol. 102: 1077-1084; Vasil, V., (1993) Bio/Technology 10: 667-674; Wan, Y. and Lemeaux, P., (1994) Plant Physiol. 104: 37-48, and for Agrobacterium-mediated DNA transfer (Ishida et al., (1996) Nature Biotech. 14: 745-750).
Typically, plant transformation vectors include one or more cloned plant coding sequences (genomic or cDNA) under the transcriptional control of 5′ and 3′ regulatory sequences and a dominant selectable marker. Such plant transformation vectors typically also contain a promoter (e.g., a regulatory region controlling inducible or constitutive, environmentally-or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, an RNA processing signal (such as intron splice sites), a transcription termination site, and/or a polyadenylation signal.
Examples of constitutive plant promoters which may be useful for expressing the CBF sequence include: the cauliflower mosaic virus (CaMV) 35S promoter, which confers constitutive, high-level expression in most plant tissues (see, e.g., Odel et al., (1985) Nature 313:810); the nopaline synthase promoter (An et al., (1988) Plant Physiol. 88:547); and the octopine synthase promoter (Fromm et al., (1989) Plant Cell 1: 977).
A variety of plant gene promoters that regulate gene expression in response to environmental, hormonal, chemical, developmental signals, and in a tissue-active manner can be used for expression of the CBFs in plants, as illustrated by seed-specific promoters (such as the napin, phaseolin or DC3 promoter described in U.S. Pat. No. 5,773,697), root-specific promoters, such as those disclosed in U.S. Pat. Nos. 5,618,988, 5,837,848 and 5,905,186; fruit-specific promoters that are active during fruit ripening (such as the dru 1 promoter (U.S. Pat. No. 5,783,393), or the 2A11 promoter (U.S. Pat. No. 4,943,674) and the tomato polygalacturonase promoter (Bird et al. (1988) Plant Mol. Biol. 11:651), root-specific promoters, such as those disclosed in U.S. Pat. Nos. 5,618,988, 5,837,848 and 5,905,186, pollen-active promoters such as PTA29, PTA26 and PTA13 (U.S. Pat. No. 5,792,929), promoters active in vascular tissue (Ringli and Keller (1998) Plant Mol. Biol. 37:977-988), flower-specific (Kaiser et al, (1995) Plant Mol. Biol. 28:231-243), auxin-inducible promoters (such as that described in van der Kop et al (1999) Plant Mol. Biol. 39:979-990 or Baumann et al. (1999) Plant Cell 11:323-334), cytokinin-inducible promoter (Guevara-Garcia (1998) Plant Mol. Biol. 38:743-753), promoters responsive to gibberellin (Shi et al. (1998) Plant Mol. Biol. 38:1053-1060, Willmott et al. (1998) 38:817-825) and the like. Additional promoters are those that elicit expression in response to light (e.g., the pea rbcS-3A promoter, Kuhlemeier et al., (1989) Plant Cell 1:471, and the maize rbcS promoter, Schaffner and Sheen, (1991) Plant Cell 3: 997); wounding (e.g., wunl, Siebertz et al., (1989) Plant Cell 1: 961); pathogen resistance chemicals such as methyl jasmonate or salicylic acid (Gatz et al., (1997) supra). In addition, the timing of the expression can be controlled by using promoters such as those acting at late seed development (Odell et al. (1994) Plant Physiol. 106:447-458).
Plant expression vectors may also include RNA processing signals that may be positioned within, upstream or downstream of the coding sequence. In addition, the expression vectors may include additional regulatory sequences from the 3′-untranslated region of plant genes, e.g., a 3′ terminator region to increase mRNA stability of the mRNA, such as the PI-II terminator region of potato or the octopine or nopaline synthase 3′ terminator regions.
Finally, as noted above, plant expression vectors may also include dominant selectable marker genes to allow for the ready selection of transformants. Such genes include those encoding antibiotic resistance genes (e.g., resistance to hygromycin, kanamycin, bleomycin, G418, streptomycin or spectinomycin) and herbicide resistance genes (e.g., phosphinothricin acetyltransferase).
The polynucleotides and polypeptides of this invention may also be expressed in a plant in the absence of an expression cassette by manipulating the activity or expression level of the endogenous gene by other means. For example, by ectopically expressing a gene by T-DNA activation tagging (Ichikawa et al. (1997) Nature 390 698-701, Kakimoto et al. (1996) Science 274: 982-985). This method entails transforming a plant with a gene tag containing multiple transcriptional enhancers and once the tag has inserted into the genome, expression of a flanking gene coding sequence becomes deregulated. In another example, the transcriptional machinery in a plant may be modified so as to increase transcription levels of a polynucleotide of the invention (See PCT Publications WO9606166 and WO 9853057 which describe the modification of the DNA binding specificity of zinc finger proteins by changing particular amino acids in the DNA binding motif).
The transgenic plant may also comprise the machinery necessary for expressing or altering the activity of a polypeptide encoded by an endogenous gene, for example by altering the phosphorylation state of the polypeptide to maintain it in an activated state.
In some cases, a reduction in the level of cryoprotectants may be desired. In such a case, a reduction of the cryoprotectant levels may be achieved by decreasing the levels of CBF expression. For example, a reduction of CBF expression in a transgenic plant to modify a plant trait may be obtained by introducing into plants antisense constructs based on the CBF cDNA. For antisense suppression, the CBF cDNA is arranged in reverse orientation relative to the promoter sequence in the expression vector. The introduced sequence need not be the full length CBF cDNA or gene, and need not be identical to the CBF cDNA or a gene found in the plant type to be transformed.
Vectors in which RNA encoded by the CBF cDNA (or variants thereof) is overexpressed may also be used to obtain co-suppression of the endogenous CBF gene in the manner described in U.S. Pat. No. 5,231,020 to Jorgensen. Such co-suppression (also termed sense suppression) does not require that the entire CBF cDNA be introduced into the plant cells, nor does it require that the introduced sequence be exactly identical to the endogenous CBF gene. However, as with antisense suppression, the suppressive efficiency will be enhanced as (1) the introduced sequence is lengthened and (2) the sequence similarity between the introduced sequence and the endogenous CBF gene is increased.
Vectors expressing an untranslatable form of the CBF mRNA may also be used to suppress the expression of endogenous CBF activity to modify a trait. Methods for producing such constructs are described in U.S. Pat. No. 5,583,021 to Dougherty et al. Preferably, such constructs are made by introducing a premature stop codon into the CBF gene. Alternatively, a plant trait may be modified by gene silencing using double-strand RNA (Sharp (1999) Genes and Development 13: 139-141) or by simultaneous expression of both sense and antisense RNAs (Waterhouse et al. (1998) Proc. Natl. Acad. Sci. USA 95: 13959-13964).
Another method for abolishing the expression of a gene is by insertion mutagenesis using the T-DNA of Agrobacterium tumefaciens. After generating the insertion mutants, the mutants can be screened to identify those containing the insertion in a CBF gene. Mutants containing a single mutation event at the desired gene may be crossed to generate homozygous plants for the mutation (Koncz et al. (1992) Methods in Arabidopsis Research. World Scientific).
A plant trait may also be modified by using the cre-lox system (for example, as described in U.S. Pat. No. 5,658,772). A plant genome may be modified to include first and second lox sites that are then contacted with a Cre recombinase. If the lox sites are in the same orientation, the intervening DNA sequence between the two sites is excised. If the lox sites are in the opposite orientation, the intervening sequence is inverted.
C. Transgenic Plants with Modified CBF Expression
Once an expression cassette comprising a polynucleotide encoding a CBF gene of this invention has been constructed, standard techniques may be used to introduce the polynucleotide into a plant in order to modify a trait of the plant. The plant may be any higher plant, including gymnosperms, monocotyledonous and dicotyledenous plants. Suitable protocols are available for Leguminosae (alfalfa (Medicago sativa), soybean (Glycine max), clover (Trifolium), etc.), Umbelliferae (carrot, celery, parsnip), Cruciferae (cabbage, radish, rapeseed (Brassica rapa L and Brassica napus L), broccoli, leaf mustard (Brassica juncea), etc.), Curcurbitaceae (melons and cucumber), Gramineae (wheat (Triticum), corn (Zea mays), rice (Oryza sativa), barley (Hordeum vulgare), rye (Secale cereale), sorghum (Sorghum bicolor and Sorghum vulgare), millet (Panicum miliaceum, Setaria italica, and Eleusine coracana), etc.), Solanaceae (potato, tomato, tobacco, peppers, etc.), and various other crops. See protocols described in Ammirato et al. (1984) Handbook of Plant Cell Culture—Crop Species. Macmillan Publ. Co; Shimamoto et al. (1989) Nature 338:274-276; Fromm et al. (1990) Bio/Technology 8:833-839; and Vasil et al. (1990) Bio/Technology 8:429-434.
Transformation and regeneration of both monocotyledonous and dicotyledonous plant cells is now routine, and the selection of the most appropriate transformation technique will be determined by the practitioner. The choice of method will vary with the type of plant to be transformed; those skilled in the art will recognize the suitability of particular methods for given plant types. Suitable methods may include, but are not limited to: electroporation of plant protoplasts; liposome-mediated transformation; polyethylene glycol (PEG) mediated transformation; transformation using viruses; micro-injection of plant cells; micro-projectile bombardment of plant cells; vacuum infiltration; and Agrobacterium tumefaciens mediated transformation. Transformation means introducing a nucleotide sequence in a plant in a manner to cause stable or transient expression of the sequence.
Successful examples of the modification of plant characteristics or traits by transformation with cloned sequences which serve to illustrate the current knowledge in this field of technology, and which are herein incorporated by reference, include: U.S. Pat. Nos. 5,571,706; 5,677,175; 5,510,471; 5,750,386; 5,597,945; 5,589,615; 5,750,871; 5,268,526; 5,780,708; 5,538,880; 5,773,269; 5,736,369 and 5,610,042.
Following transformation, plants are preferably selected using a dominant selectable marker incorporated into the transformation vector. Typically, such a marker will confer antibiotic or herbicide resistance on the transformed plants, and selection of transformants can be accomplished by exposing the plants to appropriate concentrations of the antibiotic or herbicide.
After transformed plants are selected and grown to maturity, those plants with high levels of cell protectants are identified. Additionally, to confirm that the modified trait is due to changes in expression levels or activity of the polypeptide or polynucleotide of the invention may be determined by analyzing mRNA expression using Northern blots, RT-PCR or microarrays, or protein expression using immunoblots or Western blots or gel shift assays.
The following examples are intended to illustrate but not limit the present invention.
1. Plant Handling
Arabidopsis thaliana (L.) Heynh. ecotype Ws-2 and transgenic plants in the Ws-2 background were grown in controlled environment chambers at 20° C. under constant illumination from cool-white fluorescent lights (100-150 μmol m−2 s−1)) essentially as described (Gilmour, S. J., Plant Physiol. 87:745-750 (1988)) in Baccto planting mix (Michigan Peat, Houston). Pots were sub-irrigated with deionized water as necessary. All seeds were cold-treated (5° C.) for 4 days immediately after planting to ensure uniform germination.
2. RNA Hybridization and cDNA Probes
In the following examples, unless otherwise specified, total RNA was extracted from Arabidopsis plants as described previously (Gilmour et al. (1988) Plant Physiol 87, 745-750). Northern transfers were prepared and hybridized as described (Hajela et al. (1990) Plant Physiol. 93, 1246-1252) using high stringency wash conditions (Stockinger et al. (1997) supra). 32P-labeled probes were prepared by random priming (Feinberg and Vogelstein (1983) Anal. Biochem 132, 6-13). A gene-specific probe to CBF3 was made to the 3′ end of the cDNA clone by PCR as described previously (Gilmour et al. (1998) Plant J. 16, 433-442). Arabidopsis cDNA clones encoding Arabidopsis sucrose synthase (182C20T7), corresponding to the SUS1 gene (Martin et al. (1993) Plant J. 4, 367-377) and Δ′-pyrroline-5-carboxylate synthase (125M17T7), corresponding to the P5CS2 gene (Strizhov, et al. (1997) Plant J. 12, 557-569), were obtained from the Arabidopsis Biological Resource Center at Ohio State University. Probes for P5CS2 transcripts should cross-hybridize with the highly similar P5CS1 transcripts and thus is a measure of total P5CS transcripts.
3. Isolation and Analysis of Arabidopsis Thaliana cDNA Clone (CBF1) Encoding C-Repeat/DRE Binding Factor
The following example describes the isolation of an Arabidopsis thaliana cDNA clone that encodes a C-repeat/DRE binding factor, CBF1 LC-repeat/DRE Binding Factor 1). Expression of CBF1 in yeast was found to activate transcription of reporter genes containing the C-repeat/DRE (CCGAC) as an upstream activator sequence. Meanwhile, CBF1 did not activate transcription of mutant versions of the CCGAC binding element, indicating that CBF1 is a transcription factor that binds to the C-repeat/DRE. Binding of CBF1 to the C-repeat/DRE was also demonstrated in gel shift assays using recombinant CBF1 protein expressed in Escherichia coli. Analysis of the deduced CBF1 amino acid sequence indicated that the protein has a potential nuclear localization sequence, a possible acidic activation domain and an AP2 domain, a DNA-binding motif of about 60 amino acids that is similar to those present in Arabidopsis proteins APETALA2, AINTEGUMENTA and TINY, the tobacco ethylene response element binding proteins, and numerous other plant proteins of unknown function.
Cold treatment. Plants were treated by placing pots in a cold room at 2.5° C. under cool constant illumination with white florescent lamps (25 μmol m−2s−1) for the indicated times.
Arabidopsis cDNA expression library. The Arabidopsis pACT cDNA expression library was constructed by John Walker and colleagues (NSF/DOE/USDA Collaborative Research in Plant Biology Program grant USDA 92-37105-7675) and deposited in the Arabidopsis Biological Resource Center (stock #CD4-10).
Yeast reporter strains. Oligonucleotides (Table 4) (synthesized at the MSU Macromolecular Structure Facility) encoding either wild-type or mutant versions of the C-repeat/DRE were ligated into the BglII site of the lacZ reporter vector pBgl-lacZ (Li, J. J. and 1. Herskowitz, Science 262:1870-1874 (1993); kindly provided by Joachim Li). The resulting reported constructs were integrated into the ura3 locus of Saccharomyces cerevisiae strain GGY1 (MAT gal4 gal80 ura3 leu2 his3 ade2 tyr) (Li, J. J. and 1. Herskowitz, Science 262:1870-1874 (1993); provided by Joachim Li) by transformation and selection for uracil prototrophy.
E. coli strains. Escherichia coli strain GM2163 containing plasmid pEJS251 was deposited under the Budapest Treaty on May 17, 1996 with the American Type Culture Collection, Rockville, Md. as ATCC 98063. It is available by name and number pursuant to the provisions of the Budapest Treaty.
*The C-repeat/DRE sequences tested are either wild-type found in the promoters of COR15a (Baker, S. S., et al., Plant. mol. Biol. 24: 701-713 (1994)), COR15b or COR78/RD29A (Horvath, D. P., et al., Plant Physiol. 103: 1047-1053 (1993); Yamaguchi-Shinozaki, K., et al., The Plant Cell 6: 251-264 (1994)) or are mutant versions of the COR15a C-repeat/DRE (M1COR15a, M2COR15a and M3COR15a).
#Uppercase letters designate bases in wild type C-repeat/DRE sequences. The core CCGAC sequence common to the above sequences is indicated in bold type. Lowercase letters at the beginning of a sequence indicate bases added to facilitate cloning. The lowercase letters that are underlined indicate the mutations in the C-repeat/DRE sequence of COR15a.
Screen of Arabidopsis cDNA library. The Arabidopsis pACT cDNA expression library was screened for clones encoding C-repeat/DRE environmental stress response regulatory elements by the following method. The cDNA library, harbored in Escherichia coli BNN132, was amplified by inoculating 0.5 ml of the provided glycerol stock into 1 L of M9 minimal glucose medium (Sambrook et al. (1989), supra) and shaking the bacteria for 20 h at 37° C. Plasmid DNA was isolated and purified by cesium chloride density gradient centrifugation (Sambrook et al (1989), supra) and transformed into the yeast GGY1 reporter strains selecting for leucine prototrophy. Yeast transformants that had been grown for 2 or 3 days at 30° C. were overlaid with either a nitrocellulose membrane filter (Schleicher and Schuell, Keene, N.H.) or Whatman #50 filter paper (Hillsboro, Oreg.) and incubated overnight at 30° C. The yeast impregnated filters were then lifted from the plate and treated with X-gal (5-bromo-4-chloro-3-indolyl-D-galactosidase) to assay colonies for beta-galactosidase activity (Li, J. J. and 1. Herskowitz, Science 262:1870-1874 (1993)). Plasmid DNA from “positive” transformants (those forming blue colonies on the X-gal-treated filters) was recovered (Strathern, J. N., and D. R. Higgens, Methods Enzymol. 194:319-329 (1991)), propagated in E. coli DH5α and transformed back into the yeast reporter strains to confirm activity.
Yeast transformation and quantitative beta-galactosidase assays. Yeast were transformed by either electroporation (Becker, D. M., et al., Methods Enzymol. 194:182-187 (1991)) or the lithium acetate/carrier DNA method (Schiestl, R. H., et al., Current Genetics 16:339-346 (1989)). Quantitative in vitro beta-galactosidase assays were done as described (Rose, M., et al., Methods Enzymol. 101:167-180 (1983)).
Expression of CBF1 protein in E. coli and yeast. CBF1 was expressed in E. coli using the pET-28a(+) vector (Novagen, Madison, Wis.). The BglII-BclI restriction fragment of pACT-11 encoding CBF1 was ligated into the BamHI site of the vector bringing CBF1 under control of the T7 phage promoter. The construct resulted in a “histidine tag,” a thrombin recognition sequence and a “T7 epitope tag” being fused to the amino terminus of CBF1. The construct was transformed into E. coli BL21 (DE3) and the recombinant CBF1 protein was expressed as recommended by the supplier (Novagen). Expression of CBF1 in yeast was accomplished by ligating restriction fragments encoding CBF1 (the BclI-BglII and BglII-BglII fragments from pACT-11) into the BglII site of pDB20.1 (Berger, S. L., et al., Cell 70:251-265 (1992); kindly provided by Steve Triezenberg) bringing CBF1 under control of the constitutive ADC1 (alcohol dehydrogenase constitutive 1) promoter.
Gel shift assays. The presence of expressed protein that binds to a C-repeat/DRE binding domain was evaluated using the following gel shift assay. Total soluble E. coli protein (40 ng) was incubated at room temperature in 10 μl of 1× binding buffer [15 mM HEPES (pH 7.9), 1 mM EDTA, 30 mM KCl, 5% glycerol, 5% BSA, 1 mM DTT) plus 50 ng poly(dI-dC):poly(dI-dC) (Pharmacia, Piscataway, N.J.) with or without 100 ng competitor DNA. After 10 min, probe DNA (1 ng) that was 32P-labeled by end-filling (Sambrook et al, (1989) supra) was added and the mixture incubated for an additional 10 min. Samples were loaded onto polyacrylamide gels (4% w/v) and fractionated by electrophoresis at 150V for 2 h (Sambrook et al (1989) supra). Probes and competitor DNAs were prepared from oligonucleotide inserts ligated into the BamHI site of pUC118 (Vieira, J., et al., Methods Enzymol. 153:3-11 (1987)). The orientation and concatenation number of the inserts were determined by dideoxy DNA sequence analysis (Sambrook, et al, (1989), supra). Inserts were recovered after restriction digestion with EcoRI and HindIII and fractionation on polyacrylamide gels (12% w/v) (Sambrook et al., (1989), supra).
Northern and Southern analysis. Northern and southern analysis was performed as follows. Total RNA was isolated from Arabidopsis (Gilmour, S. J., et al., Plant Physiol. 87:745-750 (1988)) and the poly(A)+ fraction purified using oligo dT cellulose (Sambrook, et al (1989), supra). Northern transfers were prepared and hybridized as described (Hajela, R. K., et al., Plant Physiol. 93:1246-1252 (1990)) except that high stringency wash conditions were at 50 C in 0.1×SSPE [×SSPE is 3.6 M NaCl, 20 mM EDTA, 0.2 M Na2—HPO4 (pH7.7)], 0.5% SDS. Membranes were stripped in 0.1×SSPE, 0.5% SDS at 95° C. for 15 min prior to re-probing. Total Arabidopsis genomic DNA was isolated (Stockinger, E. J., et al., J. Heredity, 87:214-218 (1996)) and southern transfers prepared (Sambrook et al., (1989); supra) using nylon membranes (MSI, Westborough, Mass.). High stringency hybridization and wash conditions were as described by Walling et al (Walling, L. L., et al., Nucleic Acids Res. 16:10477-10492 (1988)). Low stringency hybridization was in 6×SSPE, 0.5% SDS, 0.25% low fat dried milk at 60° C. Low stringency washes were in 1×SSPE, 0.5% SDS at 50° C. Probes used for the entire CBF1 coding sequence and 3′ end of CBF1 were the BclI/BglII and EcoRV/BglII restriction fragments from pACT-11, respectively, that had been gel purified (Sambrook et al., (1989), supra). DNA probes were radiolabeled with 32P-nucleotides by random priming (Sambrook et al., (1989), supra). Autoradiography was performed using hyperfilm-MP (Amersham, Arlington Heights, Ill.). Radioactivity was quantified using a Betascope 603 blot analyzer (Betagen Corp., Waltham, Mass.).
Screen of Arabidopsis cDNA library for sequence encoding a C-repeat/DRE binding domain. The “one-hybrid” strategy (Li, J. J. and 1. Herskowitz, Science 262:1870-1874 (1993)) was used to screen for Arabidopsis cDNA clones encoding a C-repeat/DRE binding domain. In brief, yeast strains were constructed that contained a lacZ reporter gene with either wild-type or mutant C-repeat/DRE sequences in place of the normal UAS (upstream activator sequence) of the GAL1 promoter.
Yeast strains carrying these reporter constructs produced low levels of beta-galactosidase and formed white colonies on filters containing X-gal. The reporter strains carrying the wild-type C-repeat/DRE sequences were transformed with a DNA expression library that contained random Arabidopsis cDNA inserts fused to the acidic activator domain of the yeast GAL4 transcription factor, “GAL4-ACT” (
Upon screening about 2×106 yeast transformants, three “positive” cDNA clones were isolated; i.e., clones that caused yeast strains carrying lacZ reporters fused to wild-type C-repeat/DRE inserts to form blue colonies on X-gal-treated filters (
Identification of 24 kDa polypeptide with an AP2 domain encoded by pACT-11.
Our expectation was that the cDNA insert in pACT-11 would have a C-repeat/DRE binding domain fused to the yeast GAL4-ACT sequence. However, DNA sequence analysis indicated that an open reading frame of only nine amino acids had been added to the C-terminus of GAL4-ACT. It seemed highly unlikely that such a short amino acid sequence could comprise a DNA binding domain. Also surprising was the fact that about half of the cDNA insert in pACT-11 corresponded to 25s rRNA sequences (
24 kDa polypeptide binds to the C-repeat/DRE and activates transcription in yeast. We hypothesized that the 24 kDa polypeptide was responsible for activating the lacZ reporter genes in yeast. To test this, the BclII-BglII fragment of pACT-11 containing the 24 kDa polypeptide, and the BglII-BglII fragment containing the 24 kDa polypeptide plus a small portion of the 25s rRNA sequence, was inserted into the yeast expression vector pDB20.1.
Plasmids containing either insert in the same orientation as the ADC1 promoter stimulated synthesis of beta-galactosidase when transformed into yeast strains carrying the lacZ reporter gene fused to a wild-type COR15a C-repeat/DRE (
Gel shift analysis indicates that the 24 kDa polypeptide binds to the C-repeat/DRE. Gel shift experiments were conducted to demonstrate further that the 24 kDa polypeptide bound to the C-repeat/DRE. Specifically, the open reading frame for the 24 kDa polypeptide was inserted into the pET-28a(+) bacterial expression vector (see Materials and Methods) and the resulting 28 kDa fusion protein was expressed at high levels in E. coli. (
Protein extracts prepared from E. coli expressing the recombinant protein produced a gel shift when a wild-type COR15a C-repeat/DRE was used as probe (
CBF1 is a unique or low copy number gene.
The hybridization patterns observed in southern analysis of Arabidopsis DNA using the entire CBF1 gene as probe were relatively simple indicating that CBF1 is either a unique or low copy number gene (
CBF1 transcript level response to low temperature.
Based on
Discussion. The above example regarding CBF1 represents the first identification of a gene sequence that encodes a protein capable of binding to the C-repeat/DRE sequence CCGAC. The experimental results presented evidence that CBF1 binds to the C-repeat/DRE both in vitro via gel shift assays and in vivo via yeast expression assays. Further, the results demonstrate that CBF1 can activate transcription of reporter genes in yeast that contain the C-repeat/DRE.
The results of the southern analysis indicate that CBF1 is a unique or low copy number gene in Arabidopsis. However, the CBF1 protein contains a 60 amino acid motif, the AP2 domain that is evolutionary conserved in plants (Weigel, D., The plant Cell 7:388-389 (1995)). It is present in the APETALA2 (Jofuku, K. D., et al., The Plant Cell 6:1211-1225 (1994)), AINTEGUMENTA (Klucher, K. M., et al., the Plant Cell 8:137-153 (1996; and Elliot, R. C., et al., The Plant Cell 8:155-168 (1996)), TINY (Wilson, K., et al., The Plant Cell 8:659-671 (1996)) and cadmium-induced (Choi, S.-Y., et al., Plant Physiol. 108:849 (1995)) proteins of Arabidopsis and the EREBPs of tobacco (Ohme-Takagi, M. et al., The Plant Cell 7:173-182 (1995)). In addition, a search of the GenBank expressed sequence tagged cDNA database indicates that there is one cDNA from B. napus, two from Ricinus communis, and more than 25 from Arabidopsis and 15 from rice, that are deduced to encode proteins with AP2 domains. The results of Ohme-Takagi and Shinshi (Ohme-Takagi, M., et al., The Plant Cell 7:173-182 (1995)) indicate that the function of the AP2 domain is DNA-binding; this region of the putative tobacco transcription factor EREBP2 is responsible for its binding to the cis-acting ethylene response element referred to as the GCC-repeat. As discussed by Ohme-Takagi and Shinshi (Ohme-Takagi, M., et al., the Plant Cell 7:173-182 (1995)), the DNA-binding domain of EREBP2 (the AP2 domain) contains no significant amino acid sequence similarities or obvious structural similarities with other known transcription factors or DNA binding motifs. Thus, the domain appears to be a novel DNA-binding motif that to date, has only been found in plant proteins.
It is generally believed that that the CCGAC core sequence is a member of family of core sequences having the common subsequence CCG, and that the binding of CBF1 to the C-repeat/DRE involves the AP2 domain. In this regard, it is germane to note that the tobacco ethylene response element, AGCCGCC, closely resembles the C-repeat/DRE sequences present in the promoters of the Arabidopsis genes COR15a, GGCCGAC, and COR78/RD29A, TACCGAC. Applicants believe that CBF1, the EREBPs and other AP2 domain proteins are members of a superfamily of DNA binding proteins that recognize a family of cis-acting regulatory elements having CCG as a common core sequence. Differences in the sequence surrounding the CCG core element could result in recruitment of different AP2 domain proteins which, in turn, could be integrated into signal transduction pathways activated by different environmental, hormonal and developmental cues. Such a scenario is akin to the situation that exists for the ACGT-family of cis-acting elements (Foster et al., FASEB J. 8:192-200 (1994)). In this case, differences in the sequence surrounding the ACGT core element result in the recruitment of different bZIP transcription factors involved in activating transcription in response to a variety of environmental and developmental signals. Applicants believe that other C-repeat/DRE regulatory sequences exist which belong to a broader CCG family of regulatory sequences. By screening plant genomes according to the methodology taught herein using other members of the CCG family, additional regulatory sequences as well as the binding proteins which bind to these regulatory sequences can be identified. For example, plants which are known to exhibit a form of environmental stress tolerance can be screened according to the blue colony assay and other screening methodologies used in the present invention with other members of the CCG family in order to identify other binding proteins and their gene sequences. Examples of other members of the CCG family include, but are not limited to, environmental stress response regulatory elements which include one of the following sequences: CCGAA, CCGAT, CCGAC, CCGAG, CCGTA, CCGTT, CCGTC, CCGTG, CCGCA, CCGCT, CCGCG, CCGCC, CCGGA, CCGGT, CCGGC, CCGGG, AACCG, ATCCG, ACCCG, AGCCG, TACCG, TTCCG, TCCCG, TGCCG, CACCG, CTCCG, CGCCG, CCCCG, GACCG, GTCCG, GCCCG, GGCCG, ACCGA, ACCGT, ACCGC, ACCGG, TCCGA, TCCGT, TCCGC, TCCGG, CCCGA, CCCGT, CCCGC, CCCGG, GCCGA, GCCGT, GCCGC, and GCCGG (see U.S. Pat. No. 6,417,428).
The results of the yeast transformation experiments indicate that CBF1 has a domain that can serve as a transcriptional activator. The most likely candidate for this domain is the acidic C-terminal half of the polypeptide. Indeed, random acidic amino acid peptides from E. coli have been shown to substitute for the GAL4 acidic activator domain of GAL4 in yeast (Ma, J. and M. Ptashne, Cell 51:113-199 (1987)). Moreover, acidic activator domains have been found to function across kingdoms (Hahn, S., Cell 72:481483 (1993)); the yeast GAL4 acidic activator, for instance, can activate transcription in tobacco (Ma, J., et al., Nature 334:631-633 (1988)). It has also been shown that certain plant transcription factors, such as Vp1 (McCarty, D. R., et al., Cell 66:895-905 (1991)), have acidic domains that function as transcriptional activators in plants. Significantly, the acidic activation domains of the yeast transcription factors VP16 and GCN4 require the “adaptor” proteins ADA2, ADA3, and GCN5 for full activity (see Guarente, L., Trends Biochem. Sci. 20:517-521 (1995)). These proteins form a heteromeric complex (Horiuchi, J., et al., Mol. Cell Biol. 15:1203-1209 (1995)) that bind to the relevant activation domains. The precise mechanism of transcriptional activation is not known, but appears to involve histone acetylation: there is a wealth of evidence showing a positive correlation between histone acetylation and the transcriptional activity of chromatin (Wolffe, A. P., Trends Biochem. Sci. 19:240-244 (1994)) and recently, the GCN5 protein has been shown to have histone acetyltransferase activity (Brownell, J. E., et al., Cell 84:843-851 (1996)). Genetic studies indicate that CBF1, like VP16 and GCN4, requires ADA2, ADA3 and GCN5 to function optimally in yeast. The fundamental question thus raised is whether plants have homologs of ADA2, ADA3 and GCN5 and whether these adaptors are required for CBF1 function (and function of other transcription factors with acidic activator regions) in Arabidopsis.
A final point regards regulation of CBF1 activity. The results of the northern analysis indicate that CBF1 transcript levels increase only slightly in response to low temperature, while those for COR15a increase dramatically (
4. Identification of Modified Phenotypes in Overexpression or Gene Knockout Plants
Experiments were performed to identify those transformants or knockouts that exhibited modified cell protectant levels. Among the biochemicals that were assayed were sugars, proline and fatty acids.
Proline levels in leaves were measured by preparing lyophilized leaf material; 30 mg samples of the lyophilized material were then extracted with 3 ml deionized water at 80° C. for 15 min. The samples were shaken for approximately 1 hour at room temperature and then allowed to stand overnight at 4° C. The extracts were filtered through glass wool and analyzed for proline content using the acid ninhydrin reaction (Troll and Lindsley (1955) J. Biol. Chem. 215, 655-660). Proline levels in certain samples were confirmed by amino acid analysis using an amino acid analyzer at the Macromolecular Structure Facility in the Biochemistry Department at Michigan State University.
Total soluble sugars (e.g. sucrose, glucose, and fructose among others) were extracted from lyophilized leaf material (20 mg) in 80% ethanol (2 ml) at 80° C. for 15 min. The samples were shaken for approximately 1 hr at room temperature and allowed to stand overnight at 4° C. Extracts were filtered through glass wool and chlorophyll removed by shaking samples (0.4 ml) with water (0.4 ml) and chloroform (0.4 ml). The aqueous extract was tested for sugar content using the phenol-sulfuric acid assay (Dubois et al., (1956) Anal Chem. 28, 350-356). Certain samples were dried down, suspended in water and the sugars analyzed by HPLC using a sugar column (Shodex, Shoko Co. Ltd., Japan) with a refractive index detector as previously described (Gao et al. (1999) Physiol. Plant. 106, 1-8). Retention times were compared to those of standard glucose, fructose and sucrose, and the peaks integrated using Millennium-32 software (Waters Corp.).
The fatty acid composition of plant cells and tissues may be altered by transcriptional control of fatty acid biosynthesis. The presently disclosed transcription factors and variants thereof may be able to modify the expression of fatty acid biosynthetic pathways, which may, in turn, alter cell protectant levels within a plant. A number of individual fatty acids in the leaves of transgenic plants are presently of interest as cell protectants. These fatty acids of interest represent either end products or intermediates within one or more biosynthetic pathways. Modifications of the levels of intermediates generally affect the throughput and yield of an entire pathway, and thus measurements of individual fatty acid metabolites are often representative of changes to an entire biosynthetic pathway. For example, malonyl-CoA is a common intermediate in fatty acid biosynthesis of anthroquinones, cuticular waxes, flavonoids, and fatty acids. The formation of malonyl-CoA may be regulated by the action of acetyl-CoA carboxylase, which catalyzes ATP-dependent carboxylation of acetyl-CoA to malonyl-CoA. Control of malonyl-CoA synthesis at the enzymatic or transcriptional level has a profound impact on various fatty acid levels via a number of pathways (Higuchi, T. (1997) Biochemistry and Molecular Biology of Wood, Springer-Verlag, Berlin, pp. 238-242, and Buchanan et al (2000) Biochemistry and Molecular Biology of Plants, Amer Soc Plant Physiol, Rockville, Md., pp. 465-471) e.g., saturated fatty acids such as 18:1, 18:2 and/or 18:3 fatty acids that may protect plants freezing stress). Thus, analysis of both total lipids and of individual fatty acids that affect entire pathways is central to understanding how fatty acid biosynthesis and composition can act to modulate a plant's cell protectant levels.
Total lipids from Arabidopsis leaves were measured by extraction, hydrolysis, and methylation essentially as described by Benning and Somerville ((1992) J. Bacteriol. 174, 2352-2360). Triplicate samples of leaf material (approximately 20 mg fresh weight) were placed in Teflon®-lined glass screw cap tubes with 1 ml 1 N HCl in methanol and heated at 80° C. for 40 min. Myristic acid (14:0) (5 μg) was added as an internal standard to each sample. The resulting fatty acid methyl esters were partitioned into 0.9% NaCl in hexane (1 ml), the hexane phase concentrated to a small volume and the entire sample separated by gas chromatography as detailed (Rossak et al., 1997 Arch. Biochem. Biophys. 340, 219-230). The individual fatty acids were quantified using AGP_TOP software (Hewlett Packard). Experiments were performed to identify those transformants or knockouts that exhibited an improved environmental stress tolerance, including cold or freezing stress, drought stress or salt stress, as described in the following examples. For such studies, the transformants were exposed to a variety of environmental stresses. Plants were exposed to chilling stress (6 hour exposure to 4-8° C.), heat stress (6 hour exposure to 32-37° C.), high salt stress (6 hour exposure to 200 mM NaCl), drought stress (168 hours after removing water from trays), or osmotic stress (6 hour exposure to 3 M mannitol).
5. Use of CBF1 to Induce Cold Regulated Gene Expression in Non-Cold Acclimated Arabidopsis Plants.
The following example demonstrates that increased expression of CBF1 induces COR gene expression in non-cold acclimated Arabidopsis plants. Transgenic Arabidopsis plants that overexpress CBF1 were created by placing a cDNA encoding CBF1 under the control of the strong cauliflower mosaic virus (CaMV) 35S promoter and transforming the chimeric gene into Arabidopsis ecotype RLD plants (Standard procedures were used for plasmid manipulations (Sambrook et al., (1989), supra). The CBF1-containing Asel-BglII fragment from pACT-Bgl+ (Stockinger, E. J., et al., Proc. Natl. Acad. Sci. U.S.A. 94:1035 (1997)) was gel-purified, BamHI linkers were ligated to both ends and the fragment was inserted into the BamHI site in pCIB710 (S. Rothstein, et al., Gene 53:153-161 (1987)) which contains the CaMV 35S promoter and terminator. The chimeric plasmid was linearized at the KpnI site and inserted into the KpnI site of the binary vector pCIB10g (Ciba-Geigy, Research Triangle Park, N.C.). The plasmid was transformed into Agrobacterium tumefaciens strain C58C1 (pMP90) by electroporation. Arabidopsis plants were transformed by the vacuum infiltration procedure (N. Bechtold, J. Ellis, and G. Pelletier, C. R. Acad. Sci. Paris, Life Sci. 316:1194-1199 (1993)) as modified (A. van Hoof, P. J. Green, Plant Journal 10:415-424 (1996)). Initial screening gave rise to two transgenic lines, A6 and B16, that accumulated CBF1 transcripts at elevated levels.
Southern analysis indicated that the A6 line had a single DNA insert while the B16 line had multiple inserts (not shown). Examination of fourth generation homozygous A6 and B16 plants indicated that CBF1 transcript levels were higher in non-cold acclimated A6 and B16 plants than they were in non-cold acclimated RLD plants, the levels in A6 being about three fold higher than in B16 (
CBF1 overexpression resulted in strong induction of COR gene expression (
The results from this example demonstrate that overexpression of the Arabidopsis transcriptional activator CBF1 induces expression of an Arabidopsis COR “regulon” composed of genes carrying the CRT/DRE DNA regulatory element. It appears that CBF1 binds to the CRT/DRE DNA regulatory elements present in the promoters of these genes and activates transcription that is consistent with the notion of CBF1 having a role in COR gene regulation. Significantly, there was a strong correlation between CBF1 transcript levels and the magnitude of COR gene induction in non-cold acclimated A6, B16, and RLD plants (
6. CBF1 Overexpression Resulted in a Marked Increase in Plant Freezing Tolerance
The following example describes a comparison of the freezing tolerance of non-cold acclimated Arabidopsis plants that overexpress CBF1 to that of cold-acclimated wild-type plants. As described below, the freezing tolerance of non-cold acclimated Arabidopsis plants overexpressing CBF1 significantly exceeded that of non-cold acclimated wild-type Arabidopsis plants and approached that of cold-acclimated wild-type plants.
Freezing tolerance was determined using the electrolyte leakage test (Sukumaran, N. P., et al., HortScience 7:467 (1972)). Detached leaves were frozen to various subzero temperatures and, after thawing, cellular damage (due to freeze-induced membrane lesions) was estimated by measuring ion leakage from the tissues.
As can be seen from
The results presented in
A comparison of EL50 values (the freezing temperature that results in release of 50% of tissue electrolytes) of leaves from RLD, A6, B16 and T8 plants is presented in Table 5.
EL50 values were calculated and compared by analysis of variance curves fitting up to third order linear polynomial trends were determined for each electrolyte leakage experiment. To insure unbiased predictions of electrolyte leakage, trends significantly improving the model fit at the 0.2 probability level were retained. EL50 values were calculated from the fitted models. In Table 2, an unbalanced one-way analysis of variance, adjusted for the different numbers of EL50 values for each plant type, was determined using SAS PROC GLM [SAS Institute, Inc. (1989), SAS/STAT User's Guide, Version 6, Cory, N.C.)]. EL50 values±SE (n) are presented on the diagonal line for leaves from non-cold acclimated RLD (RLDw), cold-acclimated (7 to 10 days) RLD (RLDc) and non-cold acclimated A6, B16 and T8 plants. P values for comparisons of EL50 values are indicated in the intersecting cells.
The data confirm that: 1) the freezing tolerance of leaves from both non-cold acclimated A6 and B16 plants is greater than that of leaves from both non-cold acclimated RLD and T8 plants; and 2) that leaves from non-cold acclimated A6 plants are more freezing tolerant than leaves from non-cold acclimated B16 plants. No significant difference was detected in EL50 values for leaves from non-cold acclimated A6 and cold-acclimated RLD plants or from non-cold acclimated RLD and T8 plants.
The enhancement of freezing tolerance in the A6 line was also apparent at the whole plant level.
Although the magnitude of the difference varied from experiment to experiment, non-cold acclimated A6 plants consistently displayed greater freezing tolerance in whole plant freeze tests than did non-cold acclimated RLD plants (
The results of this experiment show that CBF1-induced expression of CRT/DRE-regulated COR genes result in a dramatic increase in freezing tolerance and confirms the belief that COR genes play a major role in plant cold acclimation. The increase in freezing tolerance brought about by expressing the battery of CRT/DRE-regulated COR genes was much greater than that brought about by overexpressing COR15a alone indicating that COR genes in addition to COR15a have roles in freezing tolerance.
Traditional plant breeding approaches have met with limited success in improving the freezing tolerance of agronomic plants (Thomashow, M. F., Adv. Genet 28:99 (1990)). For instance, the freezing tolerance of the best wheat varieties today is essentially the same as the most freezing-tolerance varieties developed in the early part of this century. Thus, in recent years there has been considerable interest that biotechnology might offer new strategies to improve the freezing tolerance of agronomic plants. By the results of the present invention, Applicants demonstrate the ability to enhance the freezing tolerance of non-cold acclimated Arabidopsis plants by increasing the expressing of the Arabidopsis regulatory gene CBF1. As described throughout this application, the ability of the present invention to modify the expression of environmental stress tolerance genes such as core genes has wide ranging implications since the CRT/DRE DNA regulatory element is not limited to Arabidopsis (Jiang C., et al., Plant Mol. Biol. 30:679 (1996)). Rather, CBF1 and homologous genes can be used to manipulate expression of CRT/DRE-regulated COR genes in important crop species and thereby improve their freezing tolerance. By transforming modified versions of CBF1 (or homologs) into such plants, it will extend their safe growing season, increase yield and expand areas of production.
7. Selection of Promoters to Control Expression of CBF1 in Plants.
The following examples describe the isolation of different promoters from plant genomic DNA, construction of the plasmid vectors carrying the CBF1 gene and the inducible promoters, transformation of Arabidopsis cells/plants with these constructs, and regeneration of transgenic plants with increased tolerance to environmental stresses.
Isolation of inducible promoters from plant genomic DNAs. Inducible promoters from different plant genomic DNAs were identified and isolated by PCR amplification using primers designed to flank the promoter region and contain suitable restriction sites for cloning into the expression vector. The following genes were used to BLAST search GenBank to find the inducible promoters: Dreb2a; P5CS; Rd22; Rd29a; Rd29b; Rab18; Cor47. Table 6 lists the accession numbers and positions of these promoters. Table 7 lists the forward and reverse primers that were used to isolate the promoters.
(1) Dreb2a Promoter
A cDNA encoding DRE (C-repeat) binding protein (DREB2A) has been recently identified (Liu, et al. 1998 Plant Cell 10:1391-1406). The transcription of the DREB2A gene is activated by dehydration and high-salt stress, but not by cold stress. The upstream untranslated region (166 bps) of dreb2a was used to BLAST-search the public database. A region containing the DREB2A promoter was identified in chromosome 5 of Arabidopsis (Accession No. AB010692) between nucleotide positions 51901-53955 (Table 6).
Two PCR primers designed to amplify the promoter region from Arabidopsis thaliana genomic DNA are as follows: dreb2a-reverse:
and dreb2a-forward:
The dre2ba-reverse primer includes a Hind III (AAGCTT) restriction site near the 5′-end of the primer and dreb2a-forward primer has a Bgl II (AGATCT) restriction site at near 5′-end of the primer. These restriction sites may be used to facilitate cloning of the fragment into an expression vector.
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The reaction conditions that may be used in this PCR experiment are as follows: Segment 1: 94° C., 2 minutes; Segment 2: 94° C., 30 seconds; 60° C., 1 minute; 72° C., 3 minutes, for a total of 35 cycles; Segment 3: 72° C. for 10 minutes. A PCR product of 2054 bp is expected.
The PCR products can be subject to electrophoresis in a 0.8% agarose gel and visualized by ethidium bromide staining. The DNA fragments containing the inducible promoter will be excised and purified using a Qiaquick gel extraction kit (Qiagen, Valencia, Calif.).
(2) P5CS Promoter
A cDNA for delta 1-pyrroline-5-carboxylate synthetase (P5CS) has been isolated and characterized (Yoshiba, et al., 1995, Plant J. 7:751-760). The cDNA encodes an enzyme involved in the biosynthesis of proline under osmotic stress (drought/high salinity). The transcription of the P5CS gene was found to be induced by dehydration, high salt and treatment with plant hormone ABA, while it did not respond to heat or cold treatment.
A genomic DNA containing a promoter region of P5CS was identified by a BLAST search of GenBank using the upstream untranslated region (106 bps) of the P5CS sequence (Accession No. D32138). The sequence for the P5CS promoter is located in the region between from nucleotide positions 45472 to 47460 (Accession No. AC003000; Table 6).
Reverse and forward PCR primers designed to amplify this promoter region from Arabidopsis thaliana genomic DNA are P5CS-reverse primer
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1988 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
(3) rd22 Promoter
A cDNA clone of rd22 was isolated from Arabidopsis under dehydration conditions (Yamaguchi-Shinozaki and Shinozaki, Mol. Gen. Genet. 238:17-25 (1993)). Transcripts of rd22 were found to be induced by salt stress, water deficit and endogenous abscisic acid (ABA) but not by cold or heat stress. A promoter region was identified from GenBank by using Nucleotide Search WWW Entrez at the NCBI with the rd22 as a search word. The sequence for the rd22 promoter is located in the region between nucleotide positions 17 to 1046 (Accession No. D10703; Table 6).
Reverse and forward PCR primers designed to amplify this promoter region from Arabidopsis thaliana genomic DNA are rd22-reverse primer
The rd22-reverse primer includes a Hind III (AAGCTT) restriction site near the 5′-end of primer and rd22-forward primer has a KpnI (GGTACC) restriction site at near 5′-end of primer.
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1029 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
(4) rd29a Promoter
The rd29a and rb29b genes were isolated and characterized by Shinozaki's group in Japan (Yamaguchi-Shinizaki and Shinozaki, Plant Physiol. 101: 1119-1120 (1993)). Both rd29a and rb29b gene expressions were found to be induced by desiccation, salt stress and exogenous ABA treatment (Yamaguchi-Shinizaki and Shinozaki, Plant Physiol. 101: 1119-1120 (1993); Ishitani et al., Plant Cell 10: 1151-1161 (1998)). The rd29a gene expression was induced within 20 min after desiccation, but rd29b mRNA did not accumulate to a detectable level until 3 hours after desiccation. Expression of rd29a could also be induced by cold stress, whereas expression of rd29b could not be induced by low temperature.
A genomic clone carrying the rd29a promoter was identified by using Nucleotide Search WWW Entrez at the NCBI with the rd29a as a search word. The sequence for the rd29a promoter is located in the region between nucleotide positions 3870 to 5511 (Accession No. D13044, Table 6).
Reverse and forward primers designed to amplify this promoter region from Arabidopsis genomic DNA are: rd29a-reverse primer
The rd29a-reverse primer includes a Hind III (AAGCTT) restriction site near the 5′-end of primer and rd29a-forward primer has a KpnI (GGTACC) restriction site near 5′-end of primer.
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1641 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
(5) rd29b Promoter
A genomic clone carrying the rd29b promoter was identified by using Nucleotide Search WWW Entrez at the NCBI with the rd29b as a search word. The sequence for the rd29a promoter was located in the region between nucleotide positions 90 to 1785 for rd29b (Accession No. D13044; Table 6).
Reverse and forward PCR primers designed to amplify this promoter region from Arabidopsis thaliana genomic DNA are: rd29b-reverse primer
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1695 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
(6) rab18 Promoter
A rab-related (responsive to ABA) gene, rab18 from Arabidopsis has been isolated. The gene encodes a hydrophilic, glycine-rich protein with the conserved serine- and lysine-rich domains. The rab18 transcripts accumulate in plants exposed to water deficit or exogenous abscisic acid (ABA) treatment. A weak induction of rab18 mRNA by low temperature was also observed (Ishitani et al., Plant Cell 10: 1151-1161 (1998)).
A genomic DNA containing a promoter region of rab18 was identified by a BLAST search of GenBank using the upstream untranslated region (757 bps) of the rab18 sequence (Accession No. L04173). The sequence of the rab18 promoter is located in the region between nucleotide positions 8070 to 9757 (Accession No. AB013389).
Reverse and forward PCR primers designed and used to amplify this promoter region from Arabidopsis thaliana genomic DNA are: rab18-reverse primer
The rab18-reverse primer includes a Hind III (AAGCTT) restriction site near the 5′-end of the primer and rab18-forward primer has a Bgl II (AGATCT) restriction site near the 5′-end of the primer.
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1687 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
(7) Cor47 Promoter
The DNA sequence of cDNA for cold-regulated (cor47) gene of Arabidopsis thaliana was determined. Gilmour et al., Plant Molecular Biology 18: 13-21 (1992)). Expression of cor47 gene was induced by cold stress, dehydration and high NaCl treatment (Ishitani et al., Plant Cell, 10: 1151-1161 (1998)). The promoter region of cor47 gene was identified in GenBank by using Nucleotide Search WWW Entrez at the NCBI with the cor47 as a search word. The sequence of the cor47 promoter is located in the region between nucleotide positions 1-1370 (Accession No. AB004872; Table 6).
Reverse and forward PCR primers designed to amplify this promoter region from Arabidopsis thaliana genomic DNA are: cor47-reverse primer
The cor47-reverse primer includes a Hind III (AAGCTT) restriction site near the 5′-end of the primer and cor47-forward primer has a Bgl II (AGATCT) restriction site near the 5′-end of the primer.
Total genomic DNA may be isolated from Arabidopsis thaliana (ecotype colombia) by using the CTAB method (Ausubel et al. (1992) Current Protocols in Molecular Biology (Greene & Wiley, New York)). Ten nanograms of the genomic DNA can be used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The PCR product is expected to be 1370 bps and may be PCR amplified and gel purified following the same protocol described for the dreb2a promoter.
Construction of the plasmids containing CBF1 and inducible promoter. The expression binary vector pMEN020 contains a kanamycin resistance gene (neomycin phosphotransferase) for antibiotic selection of the transgenic plants and a Spc/Str gene used for bacterial or agrobacterial selections. The pMEN020 plasmid is digested with restriction enzymes such as HindIII and BglII to remove the 35S promoter. The 35S promoter is then replaced with an inducible promoter.
(1) Cloning of the Inducible Promoter into pMEN020
The sequences of the inducible promoters that are PCR amplified and gel purified, as well as the plasmid pMEN020, are subject to restriction digestion with their respective restriction enzymes as listed in Table 7. Both DNA samples are purified by using the Qiaquick purification kit (Qiagen) and ligated at a ratio of 3:1 (vector to insert). Ligation reactions using T4 DNA ligase (New England Biolabs, MA) are carried out at 16° C. for 16 hours. The ligated DNAs are transformed into competent cells of the E. coli strain DH5a by using the heat shock method. The transformed cells are plated on LB plates containing 100 μg/ml spectinomycin (Sigma-Aldrich). Individual colonies are grown overnight in five milliliters of LB broth containing 100 μg/ml spectinomycin at 37° C.
Plasmid DNAs from transformants are purified by using Qiaquick Mini Prep kits (Qiagen) according to the manufacturer's instruction. The presence of the promoter insert is verified by restriction mapping with the respective restriction enzymes as listed in Table 7 to cut out the cloned insert. The plasmid DNA is also subject to double-strand DNA sequencing analysis using a vector primer
(2) Cloning of the cbf1 Gene into the Plasmids Containing the Inducible Promoters
To clone the CBF1 gene into the plasmids, different PCR primers with suitable restriction sites for each plasmid are used to isolate cbf1 gene from Arabidopsis thaliana genomic DNA. The primers that may be used are listed in Table 8.
Two of the four available PCR primers (Table 8) are used for cloning the at-cbf1 gene into the expression vectors containing each inducible promoter described above. The four primers have these sequences: cbf1-reverse 1
For example, for the Dreb2a, P5CS, and COR47 promoters that are ligated to a BamHI and BglII flanked insert, the cbf1-reverse 1 and cbf1-forward 1 primers [SEQ ID NO: 34 and 35, respectively] are used to isolate cbf1 gene from Arabidopsis thaliana genomic DNA. The cbf1-reverse primer includes a BglII (AGATCT) restriction site near the 5′-end of the primer and cbf1-forward primer has a BamHI (GGATCC) restriction site near the 5′-end of the primer. A PCR product of 764 bp is expected. The genomic DNA (10 ng) is used as a template in a PCR reaction under conditions suggested by the manufacturer (Boehringer Mannheim). The reaction conditions to be used in this PCR experiment are as follows: Segment 1: 94° C., 2 minutes; Segment 2: 94° C., 30 seconds; 55° C., 1 minute; 72° C., 1 minute, for a total of 35 cycles; Segment 3: 72° C. for 10 minutes.
The PCR products are subject to electrophoresis in a 0.8% agarose gel and visualized by ethidium bromide staining. The DNA fragment containing cbf1 is excised and purified by using a Qiaquick gel extraction kit (Qiagen). The purified fragment and the vector pMB12001 containing the inducible promoter (Table 8) are each digested with BglII and BamHI restriction enzymes at 37° C. for 2 hours. Both DNA samples are purified by using the Qiaquick purification kit (Qiagen) and ligated at a ratio of 3:1 (vector to insert). Ligation reactions using T4 DNA ligase (New England Biolabs, MA) are carried out at 16° C. for 16 hours. The ligated DNAs are transformed into competent cells of the E. coli strain DH5α by using the heat shock method. The transformation are plated on LB plates containing 100 (g/ml spectinomycin (Sigma-Aldrich).
Individual colonies are grown overnight in five milliliters of LB broth containing 100 g/ml spectinomycin at 37° C. Plasmid DNA are purified by using Qiaquick Mini Prep kits (Qiagen). The presence of the cbf1 insert is verified by restriction mapping with BglII and BamHI. The plasmid DNA is also subject to double-strand DNA sequencing analysis by using vector primer
The other primers shown in Table 8 and appropriate restriction enzymes are used in a similar way to clone the Cbf1 gene into plasmids containing the other inducible promoters. The resulting plasmids are listed in Table 9 and shown in
A similar cloning strategy may be used to clone other genes, such as cbf2, cbf3, and the other full length CBF genes listed in Table 9 and shown in
8. Transformation of Agrobacterium with Plasmids Containing CBF1 Gene and Inducible Promoters
After the plasmid vectors containing cbf1 gene and inducible promoters are constructed, these vectors are used to transform Agrobacterium tumefaciens cells expressing the gene products. The stock of Agrobacterium tumefaciens cells for transformation are made as described by Nagel et al. FEMS Microbiol Letts 67: 325-328 (1990). Agrobacterium strain ABI is grown in 250 ml LB medium (Sigma-Aldrich) overnight at 28° C. with shaking until an absorbance (A600) of 0.5-1.0 is reached. Cells are harvested by centrifugation at 4,000×g for 15 min at 4 C. Cells are then resuspended in 250 μl chilled buffer (1 mM HEPES, pH adjusted to 7.0 with KOH). Cells are centrifuged again as described above and resuspended in 125 μl chilled buffer. Cells are then centrifuged and resuspended two more times in the same HEPES buffer as described above at a volume of 100 μl and 750 μl, respectively. Resuspended cells are then distributed into 40 μl aliquots, quickly frozen in liquid nitrogen, and stored at −80 C.
Agrobacterium cells are transformed with plasmids formed as described above in Section 4B(2) following the protocol described by Nagel et al. FEMS Microbiol Letts 67: 325-328 (1990). For each DNA construct to be transformed, 50-100 ng DNA (generally resuspended in 10 mM Tris-HCl, 1 mM EDTA, pH 8.0) is mixed with 40 μl of Agrobacterium cells. The DNA/cell mixture is then transferred to a chilled cuvette with a 2 mm electrode gap and subject to a 2.5 kV charge dissipated at 25 μF and 200 μF using a Gene Pulser II apparatus (Bio-Rad, Hercules, Calif.). After electroporation, cells are immediately resuspended in 1.0 ml LB and allowed to recover without antibiotic selection for 2-4 hours at 28° C. in a shaking incubator. After recovery, cells are plated onto selective medium of LB broth containing 100 μg/ml spectinomycin (Sigma-Aldrich) and incubated for 24-48 h at 28° C. Single colonies are then picked and inoculated in fresh medium. The presence of the plasmid construct are verified by PCR amplification and sequence analysis.
9. Transformation of Arabidopsis Plants with Agrobacterium tumefaciens Carrying Expression Vector for CBF1 Protein
After transformation of Agrobacterium tumefaciens with plasmid vectors containing cbf1 gene and inducible promoters, single Agrobacterium colonies containing each of pMB12008-pMB12014 are identified, propagated, and used to transform Arabidopsis Plants. Briefly, 500 ml cultures of LB medium containing 100 ug/ml spectinomycin are inoculated with the colonies and grown at 28 C with shaking for 2 days until an absorbance (A600) of >2.0 is reached. Cells are then harvested by centrifugation at 4,000×g for 10 min, and resuspended in infiltration medium (½× Murashige and Skoog salts (Sigma-Aldrich), 1× Gamborg's B-5 vitamins (Sigma-Aldrich), 5.0% (w/v) sucrose (Sigma-Aldrich), 0.044 μM benzylamino purine (Sigma-Aldrich), 200 μl/L Silwet L-77 (Lehle Seeds) until an absorbance (A600) of 0.8 is reached.
Prior to transformation, Arabidopsis thaliana seeds (ecotype Columbia) are sown at a density of ˜10 plants per 4″ pot onto Pro-Mix BX potting medium (Hummert International) covered with fiberglass mesh (18 mm×16 mm). Plants are grown under continuous illumination (50-75 μE/m2/sec) at 22-23 C with 65-70% relative humidity. After about 4 weeks, primary inflorescence stems (bolts) are cut off to encourage growth of multiple secondary bolts. After flowering of the mature secondary bolts, plants are prepared for transformation by removal of all siliques and opened flowers.
The pots are then immersed upside down in the mixture of Agrobacterium/infiltration medium as described above for 30 sec, and placed on their sides to allow draining into a 1′×2′ flat surface covered with plastic wrap. After 24 h, the plastic wrap is removed and pots are turned upright. The immersion procedure is repeated one week later, for a total of two immersions per pot. Seeds are then collected from each transformation pot and analyzed following the protocol described below.
10. Identification of Arabidopsis Primary Transformants
Seeds collected from the transformation pots are sterilized essentially as follows. Seeds are dispersed into in a solution containing 0.1% (v/v) Triton X-100 (Sigma-Aldrich) and sterile H2O and washed by shaking the suspension for 20 min. The wash solution is then drained and replaced with fresh wash solution to wash the seeds for 20 min with shaking. After removal of the second wash solution, a solution containing 0.1% (v/v) Triton X-100 and 70% EtOH (Equistar) is added to the seeds and the suspension is shaken for 5 min. After removal of the ethanol/detergent solution, a solution containing 0.1% (v/v) Triton X-100 and 30% (v/v) bleach (Chlorox) is added to the seeds, and the suspension is shaken for 10 min. After removal of the bleach/detergent solution, seeds are then washed five times in sterile distilled H2O. The seeds are stored in the last wash water at 4° C. for 2 days in the dark before being plated onto antibiotic selection medium (1× Murashige and Skoog salts (pH adjusted to 5.7 with 1 M KOH), 1× Gamborg's B-5 vitamins, 0.9% phytagar (Life Technologies, Rockville, Md.), and 50 μg/L kanamycin). Seeds are germinated under continuous illumination (50-75 μE/m2/sec) at 22-23° C. After 7-10 days of growth under these conditions, kanamycin resistant primary transformants (T1 generation) are visible and are obtained for each of constructs pMB12008-pMB12014. These seedlings are transferred first to fresh selection plates where the seedlings continued to grow for 3-5 more days, and then to soil (Pro-Mix BX potting medium). Progeny seeds (T2) are collected; kanamycin resistant seedlings selected and analyzed as described above.
11. Transformation of Cereal Plants with Plasmid Vectors Containing cbf1 Gene and Inducible Promoters.
Cereal plants, such as corn, wheat, rice, sorghum and barley, can also be transformed with the plasmid vectors containing the cbf genes and inducible promoters to increase their tolerance to environmental stresses. In these cases, the cloning vector, pMEN020, is modified to replace the NptII coding region with the BAR gene of Streptomyces hygroscopicus that confers resistance to phosphinothricin. The KpnI and BglII sites of the Bar gene are removed by site-directed mutagenesis with silent codon changes. After cloning of the inducible promoters into the modified plasmid by the same procedures described above, the at-cbf coding region of cbf1 gene is inserted into the plasmid following the same procedures as described above. The resulting plasmids are listed in Table 10.
It is now routine to produce transgenic plants of most cereal crops (Vasil, I., Plant Molec. Biol. 25: 925-937 (1994)) such as corn, wheat, rice, sorghum (Cassas, A. et al., Proc. Natl. Acad Sci USA 90: 11212-11216 (1993) and barley (Wan, Y. and Lemeaux, P. Plant Physiol. 104:37-48 (1994) Other direct DNA transfer methods such as the microprojectile gun or Agrobacterium tumefaciens-mediated transformation can be used for corn (Fromm. et al. Bio/Technology 8: 833-839 (1990); Gordon-Kamm et al. Plant Cell 2: 603-618 (1990); Ishida, Y., Nature Biotechnology 14:745-750 (1990)), wheat (Vasil, et al. Bio/Technology 10:667-674 (1992); Vasil et al., Bio/Technology 11:1553-1558 (1993); Weeks et al., Plant Physiol. 102:1077-1084 (1993)), rice (Christou Bio/Technology 9:957-962 (1991); Hiei et al. Plant J. 6:271-282 (1994); Aldemita and Hodges, Planta 199:612-617; Hiei et al., Plant Mol. Biol. 35:205-18 (1997)). For most cereal plants, embryogenic cells derived from immature scutellum tissues are the preferred cellular targets for transformation (Hiei et al., Plant Mol. Biol. 35:205-18 (1997); Vasil, Plant Molec. Biol. 25: 925-937 (1994)).
Plasmids according to the present invention may be transformed into corn embryogenic cells derived from immature scutellar tissue by using microprojectile bombardment, with the A188XB73 genotype as the preferred genotype (Fromm, et al., Bio/Technology 8: 833-839 (1990); Gordon-Kamm et al., Plant Cell 2: 603-618 (1990)). After microprojectile bombardment the tissues are selected on phosphinothricin to identify the transgenic embryogenic cells (Gordon-Kamm et al., Plant Cell 2: 603-618 (1990)). Transgenic plants are regenerated by standard corn regeneration techniques (Fromm, et al., Bio/Technology 8: 833-839 (1990); Gordon-Kamm et al., Plant Cell 2: 603-618 (1990)).
The plasmids prepared as described above can also be used to produce transgenic wheat and rice plants (Christou, Bio/Technology 9:957-962 (1991); Hiei et al., Plant J. 6:271-282 (1994); Aldemita and Hodges, Planta 199:612-617 (1996); Hiei et al., Plant Mol. Biol. 35:205-18 (1997)) by following standard transformation protocols known to those skilled in the art for rice and wheat Vasil, et al. Bio/Technology 10:667-674 (1992); Vasil et al., Bio/Technology 11:1553-1558 (1993); Weeks et al., Plant Physiol. 102:1077-1084 (1993)), where the BAR gene is used as the selectable marker.
12. Transformation of Plants with Plasmid Vectors Containing CBF1 Gene and Seed Specific Promoters.
The napin promoter from Brassica campestris (GenBank accession no. M64632) is a seed specific promoter. A fragment of the napin promoter (between nucleotides 1146 to 2148) is identified and isolated by PCR amplification using a 5′ PCR primer containing a HindIII site upstream of the promoter and a 3′ PCR primer containing a BamHI site downstream of the promoter. Deletion of the napin promoter to −211 and −152 have been shown to have reduced levels of expression (Ellerstrom et al., Plant Mol Biol 32: 1019-27 (1996); Stalberg et al., Planta 199: 515-9 (1996); Stalberg et al., Plant Mol Biol 23: 671-83 (1993)). These 5′ deleted promoters are useful to have reduced levels of CBF1 expression for applications where the larger napin promoter fragment is too large.
Other seed-active promoters or deletions of these promoters can also be isolated from genomic DNA by using the same method described above for the napin promoter. Examples of these promoters include but are not limited to the soybean 7S seed storage protein (Chen et al., Devel Gen 10: 112-22 (1989), the bean phaseolin promoter (cited in U.S. Pat. No. 5,003,045), the Arabidopsis 12S globulin (cruciferin) promoter (Pang et al., Plant Mol. Biol. 11: 805-820 (1988), the maize globulin1 promoter (Kriz et al., Plant Physiol. 91: 636 (1989); U.S. Pat. No. 5,773,691). These promoters may be used for altering COR gene expression in cereals such as corn, barley, wheat, rice and rye seeds.
The binary constructs containing seed-specific napin promoters (pMEN1001.1-4; pMEN1002.1-4; and pMEN1003.1-4) are used to transform canola and rapeseed plants as described (Moloney et al. U.S. Pat. No. 5,750,871), except that the Bar gene selectable marker is used.
These constructs are also used to transform regenerable barley cells by microprojectile bombardment (Wan and Lemaux, Plant Physiol. 104: 37-48 (1994)). After bombardment the tissues are selected on phosphinothricin by standard barley regeneration techniques (Wan and Lemaux, supra).
13. Identification of Homologous Sequence To CBF1 in Canola
This example describes the identification of homologous sequences to CBF1 in canola using PCR. Degenerate primers were designed for regions of AP2 binding domain and outside of the AP2 (carboxyl terminal domain). More specifically, the following degenerate PCR primers were used:
Y: C/T, N: A/C/G/T, H: A/C/T, M: A/C, R: A/G)
Primer Mol 368 is in the AP2 binding domain of CBF1 (amino acid sequence: H P I Y R G V) while primer Mol 378 is outside the AP2 domain (carboxyl terminal domain)(amino acid sequence: M A E G M L L P).
The genomic DNA isolated from Brassica Napus was PCR amplified by using these primers following these conditions: an initial denaturation step of 2 min at 93° C.; 35 cycles of 93° C. for 1 min, 55° C. for 1 min, and 72° C. for 1 min; and a final incubation of 7 min at 72° C. at the end of cycling.
The PCR products were separated by electrophoresis on a 1.2% agarose gel and, transferred to nylon membrane and hybridized with the AT CBF1 probe prepared from Arabidopsis genomic DNA by PCR amplification. The hybridized products were visualized by colorimetric detection system (Boehringer Mannheim) and the corresponding bands from a similar agarose gel were isolated (By Qiagen Extraction Kit). The DNA fragments were ligated into the TA clone vector from TOPO TA Cloning Kit (Invitrogen) and transformed into E. coli strain TOP10 (Invitrogen).
Seven colonies were picked and the inserts were sequenced on an ABI 377 machine from both strands of sense and antisense after plasmid DNA isolation. The DNA sequence was edited by sequencer and aligned with the AtCBF1 by GCG software and NCBI blast searching.
As illustrated in
14. Identification of Homologous Sequence to CBF1 in Canola and Other Species
A PCR strategy similar to that described in Example 13 was used to isolate additional CBF homologues from Brassica juncea, Brassica napus, Brassica oleracea, Brassica rapa, Glycine max, Raphanus sativus and Zea mays. The nucleotide (e.g. bjCBF1) and peptide sequences (e.g. BJCBF1-PEP) of these isolated CBF homologues are shown in
*Percentage identity to the CBF1 (SEQ ID NO: 2) AP2 region of derived polypeptide, wherein the AP2 region is defined by the AP2 consensus sequence and bounded by: HP-Y-GVR---ADS
As can be seen from the consensus sequence shown in
As can be seen from the consensus sequence shown in
As can be seen from the consensus sequence shown in
As can be seen from the consensus sequence shown in
While the present invention is disclosed by reference to the preferred embodiments and examples detailed above, it is to be understood that these examples are intended in an illustrative rather than limiting sense, as it is contemplated that modifications will readily occur to those skilled in the art, which modifications will be within the spirit of the invention and the scope of the appended claims.
15. Homologous CBF Encoding Genes in Other Plants.
This example shows that homologous sequences to CBF1 are present in other plants. The presence of these homologous sequences suggest that the same or similar cold regulated environmental stress response regulatory elements such as the C-repeat/DRE of Arabidopsis (CCGAC) exist in other plants. This example serves to indicate that genes with significant homology to CBF1, CBF2 and CBF3 exist in a wide range of plant species.
Total plant DNAs from Arabidopsis thaliana, Nicotiana tabacum, Lycopersicon pimpinellifolium, Prunus avium, Prunus cerasus, Cucumis sativus, and Oryza sativa were isolated according to Stockinger al (Stockinger, E. J., et al., J. Heredity, 87:214-218 (1996)). Approximately 2 to 10 μg of each DNA sample was restriction digested, transferred to nylon membrane (Micron Separations, Westboro, Mass.) and hybridized according to Walling et al. (Walling, L. L., et al., Nucleic Acids Res. 16:10477-10492 (1988)). Hybridization conditions were: 42° C. in 50% formamide, 5×SSC, 20 mM phosphate buffer 1× Denhardt's, 10% dextran sulfate, and 100 μg/ml herring sperm DNA. Four low stringency washes at RT in 2×SSC, 0.05% Na sarcosyl and 0.02% Na4 pyrophosphate were performed prior to high stringency washes at 55° C. in 0.2×SSC, 0.05% Na sarcosyl and 0.01% Na4 pyrophosphate. High stringency washes were performed until no counts were detected in the washout. The BclI-BglII fragment of CBF1 (Stockinger et al., Proc Natl Acad Sci USA 94:1035-1040 (1997)) was gel isolated (Sambrook et al., (1989), supra) and direct prime labeled (Feinberg and Vogelstein, Anal. Biochem 132: 6-13 (1982)) using the primer MT117
(TTGGCGGCTACGAATCCC; SEQ ID NO: 16).
Specific activity of the radiolabelled fragment was approximately 4×108 cpm/μg. Autoradiography was performed using HYPERFILM-MP (Amersham) at −80° C. with one intensifying screen for 15 hours.
Autoradiography of the gel showed that DNA sequences from Arabidopsis thaliana, Nicotiana tabacum, Lycopersicon pimpinellifolium, Prunus avium, Prunus cerasus, Cucumis sativus, and Oryza sativa hybridized to the labeled BclI, BglII fragment of CBF1. These results suggest that homologous CBF encoding genes are present in a variety of other plants.
16. Identification of CBF1 Homologs CBF2 and CBF3 Using CBF1
This example describes two homologs of CBF1 from Arabidopsis thaliana and named them CBF2 and CBF3.
CBF2 and CBF3 have been cloned and sequenced as described below. The sequences of the DNA and encoded proteins are set forth in SEQ ID NOs: 12, 13, 14 and 15, and
A lambda cDNA library prepared from RNA isolated from Arabidopsis thaliana ecotype Columbia (Lin and Thomashow, Plant Physiol. 99: 519-525 (1992)) was screened for recombinant clones that carried inserts related to the CBF1 gene (Stockinger, E. J., et al., Proc Natl Acad Sci USA 94:1035-1040 (1997)). CBF1 was 32P-radiolabeled by random priming (Sambrook et al., (1989), supra) and used to screen the library by the plaque-lift technique using standard stringent hybridization and wash conditions (Hajela, R. K., et al., Plant Physiol 93:1246-1252 (1990); Sambrook et al., (1989), supra;) 6×SSPE buffer, 60° C. for hybridization and 0.1×SSPE buffer and 60° C. for washes). Twelve positively hybridizing clones were obtained and the DNA sequences of the cDNA inserts were determined at the MSU-DOE Plant Research Laboratory sequencing facility. The results indicated that the clones fell into three classes. One class carried inserts corresponding to CBF1. The two other classes carried sequences corresponding to two different homologs of CBF1, designated CBF2 and CBF3. The nucleic acid sequences and predicted protein coding sequences for CBF1, CBF2 and CBF3 appear in
A comparison of the nucleic acid sequences of CBF1, CBF2 and CBF3 indicate that they are 83 to 85% identical as shown in Table 12.
aPercent identity was determined using the Clustal algorithm from the Megalign program (DNASTAR, Inc.).
bComparisons of the nucleic acid sequences of the open reading frames are shown.
Similarly, the amino acid sequences of the three CBF polypeptides range from 84 to 86% identity. An alignment of the three amino acidic sequences reveals that most of the differences in amino acid sequence occur in the acidic C-terminal half of the polypeptide. This region of CBF1 serves as an activation domain in both yeast and Arabidopsis (not shown).
Residues 47 to 106 of CBF1 correspond to the AP2 domain of the protein, a DNA binding motif that to date, has only been found in plant proteins. A comparison of the AP2 domains of CBF1, CBF2 and CBF3 indicates that there are a few differences in amino acid sequence. These differences in amino acid sequence might have an effect on DNA binding specificity.
17. Activation of Transcription in Yeast Containing C-repeat/DRE Using CBF1, CBF2 and CBF3
This example shows that CBF1, CBF2 and CBF3 activate transcription in yeast containing CRT/DREs upstream of a reporter gene. The CBFs were expressed in yeast under control of the ADC1 promoter on a 2μ plasmid (pDB20.1; Berger, S. L., et al., Cell 70:251-265 (1992)). Constructs expressing the different CBFs were transformed into yeast reporter strains that had the indicated CRT/DRE upstream of the lacZ reporter gene. Copy number of the CRT/DREs and its orientation relative to the direction of transcription from each promoter is indicated by the direction of the arrow.
18. Identification and Isolation of Novel CBF-Related Polypeptides
Additionally, we identified novel CBF-related polypeptides from soybean, wheat, rice and rye plants.
Soybean seeds were bought from a local supermarket (packaged by JAMECO Co, San Francisco, Calif.). DNA and mRNA were isolated using standard procedures (Ausubel et al. (1998) Current Protocols in Molecular Biology (Greene & Wiley, New York)). A soybean seedling cDNA library was also constructed using standard procedures. Based on the sequence of the Arabidopsis CBF1 gene (SEQ ID NO: 1), degenerate primers
were designed. O376 and O2953 were first used in a PCR experiment using soybean genomic DNA as template. The product from this reaction was excised from the gel, purified (Ausubel et al. (1998) supra), and used as a template in a second round of PCR using primers O368 and O376. Then, the PCR product was cloned into pGEM-T and sequenced using T7 and sp6 primers (Promega Corp).
Based on the sequence of the cloned soybean clone, 3′ rapid amplification of cDNA ends (RACE) was performed using the Marathon™ cDNA amplification kit (Clontech, Palo Alto, Calif.). Generally, the method entailed first isolating poly(A) mRNA, synthesize first and second strand cDNA to generate double stranded cDNA, blunting cDNA ends, followed by ligation of the Marathon™ Adaptor to the cDNA to form a library of adaptor-ligated double-stranded cDNA. Gene-specific primers were designed to be used along with adaptor specific primers for 3′ RACE reactions. Often, nested primers were used to increase PCR specificity. In this case, the 3′ nested primers were
The resulting RACE fragment was cloned into the pGEM-T vector (Promega Corp) and sequenced using T7 and sp6 primers. The cloned insert was then labeled using the DIG DNA Labeling and Detection Kit following the manufacture's instructions (Boehringer Mannheim), and the labeled probe was used to screen the soybean cDNA library using standard procedures and hybridization conditions (Ausubel et al. (1998) supra). SEQ ID NO: 17 was isolated in this manner.
Rice seeds were obtained from the laboratory of Dr. Pam Ronald at UC Davis. Corn, wheat, and rye seeds were obtained from the USDA, ARS National Small Grains Research Facility, Aberdeen, Id. DNA and mRNA were isolated using standard procedures. Seedling cDNA libraries were also constructed using standard procedures.
In order to isolate CBF1 homologs from monocotyledon species, CBF1 polypeptide sequence was used to identify related sequences from public plant sequence databases. The tblastn sequence analysis program was employed. A rice homologue (Acc. No. AB023482) was identified as having a P value of 6.3e-17. Based on its sequence, primers
were synthesized, and the rice gene was isolated from rice genomic DNA by a standard PCR procedure using those primers. The amplified fragment was cloned into the pGEM-T vector following the manufacture's protocol (Promega Corp). The clone was sequenced using O18016, O18017,
Based on the rice sequence, primers
were synthesized. These primers were used to isolate rye and wheat CBF gene fragments by PCR from their respective cDNA libraries. For some of the PCR reactions outlined above, a PCR optimization kit (Boehringer Mannheim) was used. The PCR product was cloned into the pGEM-T vector (Promega Corp). To isolate full-length rye cDNAs, the rye fragment was then labeled with 32P dCTP using the High Prime DNA Labeling Kit (Boehringer Mannheim). Purified radiolabeled probes were used to probe a rye cDNA library using standard conditions (Current protocols in Molecular Biology, section 6.3). SEQ ID Nos. 115, 117, 119, 121 and 123, which are rye CBF-related sequences, were isolated in this manner. SEQ ID NO: 125 is a CBF-related sequence identified from wheat.
The percent sequence identity of the AP2 regions of polypeptide SEQ ID Nos: 116, 118, 120, 122, 124 and 126, with CBF1, (SEQ ID NO: 2) are shown in Table 13. The percent sequence identity between the different polypeptides provided in the Sequence Listing varied from 53% to 96% over most of the length of the sequences. Generally, these sequences comprise an AP2 domain comprising amino acids 45, 49-52, 54, 60-61, 64, 65, 72, 74, 76, 77, 80, 82, 85, 86, 88, 89, 91, 94, 95, 100, 102-109 of SEQ ID NO: 2 or comprise one or more of the following peptides: PKXXAGR (amino acids 31-37 of SEQ ID NO: 2), or AGRXKF (amino acids 35-40 of SEQ ID NO: 2) or ETRHP (amino acids 4246 of SEQ ID NO: 2).
*Percentage identity to the CBF1 (SEQ ID NO: 2) AP2 region of derived polypeptide, wherein the AP2 region is defined by the AP2 consensus sequence and bounded by: HP-Y-GVR---ADS
19. Overexpression of CBF1 or CBF2 Increases Arabidopsis Drought or High Salt Tolerance
Soil studies were done by growing seedlings for 10 days with water, and then letting the soil dry out (no further watering) until the plants were severely dehydrated. The soil was then watered and then recovery of the plants was measured. The transgenic lines were alternated with the control wild type lines, with a one-inch spacing between plants in two inches of soil. No detrimental effects were observed but the beneficial effects seen need further testing with drought inducible promoter lines.
Two separate root elongation assays were performed to evaluate the drought resistance phenotypes of the transgenic plants. First plants were grown on MS agar plates for two weeks, and then transferred to MS agar plates containing either 300 mM mannitol or 150 mM NaCl. Those concentrations were chosen because preliminary testing showed that wild type plants showed the most dramatic reduction in root growth in those conditions. The root lengths were then measured after seven days, and the data summarized in Table 14. The growth on sucrose (0.3% w/v), the non-inhibition control and the growth on either salt or mannitol is shown. The control line lacking a CBF gene is the 643-3 line. When the ratio of the CBF line to the 643-3 line (CBF/wild type) is significantly above 1.0, this is an indication of drought or salt tolerance.
From these, we concluded that the overexpression of the CBF genes did provide growth benefit under high osmotic pressure and high salt, particularly for the CBF2 lines tested.
20. Identification of Transgenic Arabidopsis Plants that Express CBF3
Total soluble protein was obtained essentially as described (Gilmour et al., (1996) Plant Physiol. 111, 293-299) by grinding leaf material (about 100 mg) in 0.4 ml extraction buffer (50 mM PIPES pH 7.0, 25 mM EDTA) containing 2.5% (w/v) polyvinyl-polypyrrolidone and removing insoluble material by centrifugation (16000 g×20 min). Protein concentration in the supernatant was measured using the dye-binding method of Bradford (1976) with BSA as the standard. Protein samples (50 μg total protein) were fractionated by tricine SDS/PAGE (Schägger and von Jagow (1987) Anal. Biochem. 166, 368-379) and transferred to 0.2 micron nitrocellulose membranes by electroblotting. COR15am and COR6.6 were detected using the ECL kit (Amersham) with antiserum raised to recombinant COR15am and COR6.6 (Gilmour et al. (1996) Plant Physiol. 111, 293-299).
Transgenic Arabidopsis plants that overexpress CBF3 at normal growth temperature were created by placing the CBF3 coding sequence under control of the cauliflower mosaic virus (CaMV) 35S promoter and transforming the construct into Arabidopsis plants using the floral dip transformation procedure. Transgenic Arabidopsis plants that overexpress CBF3 were generated by transforming the chimeric genes into Arabidopsis ecotype Ws-2 plants.
A 910 bp BamHI/HindIII fragment from a cDNA clone containing the whole coding region of CBF3 (Gilmour et al., (1998) Plant J. 16, 433-442) was inserted into the BglII and HindIII sites of the binary transformation vector pGA643. PGA643 has a CaMV 35S promoter and the terminator from gene 7 of pTiA6 (An, “Binary Vectors”, Gynheung et al. eds (1988) Plant Molecular Biology Manual, Kluwer Acad. Publishers). The resulting plasmid, pMPS13, which contains the CBF3 coding sequence under control of the CaMV 35S promoter, was transformed into Agrobacterium tumefaciens strain GV3101 by electroporation (Koncz et al. (1986) Mol. Gen. Gen. 204: 383). Arabidopsis plants were transformed with plasmid pMPS13 or the transformation vector pGA643 using the floral dip method (Clough and Bent, (1998) Plant J. 16, 735-743). Transformed plants were selected on the basis of kanamycin resistance. Homozygous T3 or T4 plants were used in all experiments.
Standard procedures were used for plasmid manipulations (Sambrook et al., (1989), supra). Prior to transformation, Arabidopsis thaliana seeds were sown at a density of ˜10 plants per 4″ pot onto Bacto planting mix (Michigan Peat Co., Houston, Tex.) covered with fiberglass mesh (18 mm×18 mm). Plants were grown under continuous illumination (100-150 μE/m2/sec) at 20-22° C. with 65-70% relative humidity. Plants were used when the primary inflorescences were approximately 10-12 cm high. The pots were then immersed upside down in the mixture of Agrobacterium infiltration medium as described above (Clough and Bent, supra) for 2-3 seconds, and placed on their sides to allow draining into a 1′×2′ flat surface covered with plastic wrap. After 24 hours, the plastic wrap is removed and the pots were turned upright. Seeds were then collected from each transformation pot and analyzed following the protocol described below.
A construct comprising a cold-regulatable polypeptide gene coding sequence (CBF3) operably linked to a constitutive promoter was generated.
Twenty-two independent lines were identified in which the T2 plants segregated 3:1 for kanamycin resistance (the selectable marker carried on the transformation vector). These lines presumably carried a single active T-DNA locus. The kanamycin resistant T2 plants were then screened by western analysis for constitutive expression of COR15a, a target gene of the CBF transcriptional activators.
Three independent transgenic lines—A28, A30 and A40—were identified that produced the COR15am polypeptide at high levels uniformly among plants grown at normal temperatures. Northern analysis indicated that the transcript levels for CBF3 were about equal in non-cold acclimated and cold-treated A28, A30 and A40 plants and were much greater than those observed in either non-cold acclimated or cold-treated control plants (i.e. non-transformed plants or transgenic plants carrying the transformation vector without an insert). The transcript levels for two target COR genes, COR15a and COR6.6, were also nearly equal in non-cold acclimated and cold-treated A28, A30 and A40 plants and approximated the levels observed in cold-acclimated control plants. Western analysis indicated that the proteins encoded by COR15a and COR6.6 were present in both non-cold acclimated and cold-acclimated A28, A30 and A40 plants at 3 to 5 fold-higher levels than those found in cold-acclimated control plants.
21. Salinity Tolerance of Canola after Transformation with Plasmids Containing CBF1, CBF2, or CBF3
Canola was transformed with a plasmid containing the Arabidopsis CBF1, CBF2, or CBF3 genes cloned into the vector pGA643 (G. An (1987) Methods in Enzymol. 253: 292). In these constructs the CBF genes were expressed constitutively under the CaMV 35S promoter. In addition, the CBF1 gene was cloned under the control of the Arabidopsis COR15 promoter in the same vector pGA643. Each construct was transformed into Agrobacterium strain GV3101. Transformed agrobacteria was grown for 2 days in Minimal AB medium containing the appropriate antibiotics.
Spring canola (B. napus cv. Westar) was transformed using the protocol of Moloney (Moloney et. al. (1989) Plant Cell Reports 8, 238) with some modifications as described. Briefly, seeds were sterilized and plated on half strength MS medium, containing 1% sucrose. Plates were incubated at 24° C. under 60-80 uE/m2s light using a 16 hour light/8 hour dark photoperiod. Cotyledons from 4-5 day old seedlings were collected, the petioles cut and dipped into the Agrobacterium solution. The dipped cotyledons were placed on co-cultivation medium at a density of 20 cotyledons/plate and incubated as described above for 3 days. Explants were transferred to the same media, but containing 300 mg/L timentin (GlaxoSmithKline, PA) and thinned to 10 cotyledons/plate. After 7 days explants were transferred to Selection/Regeneration medium. Transfers were continued every 2-3 weeks (2 or 3 times) until shoots had developed. Shoots were transferred to Shoot-Elongation medium every 2-3 weeks. Healthy looking shoots were transferred to rooting medium. Once good roots had developed, the plants were placed into moist potting soil.
The transformed plants were then analyzed for the presence of the NPTII gene/kanamycin resistance by Elisa, using the Elisa NPTII kit from 5Prime-3Prime Inc. (Boulder, Colo.). Approximately 70% of the screened plants were NPTII positive. Only those plants were further analyzed.
From Northern blot analysis of the plants that were transformed with the constitutively expressing constructs, showed expression of the CBF genes and all CBF genes were capable of inducing the Brassica napus cold-regulated gene BN115 (homolog of the Arabidopsis COR15 gene). Most of the transgenic plants appear to exhibit a normal growth phenotype. As expected, the transgenic plants are more freezing tolerant than the wild-type plants. Using the electrolyte leakage of leaves test, the control showed a 50% leakage at −2 to −3° C. Spring canola transformed with either CBF1 or CBF2 showed a 50% leakage at −6 to −7° C. Spring canola transformed with CBF3 shows a 50% leakage at about −10 to −15° C. Winter canola transformed with CBF3 may show a 50% leakage at about −16 to −20° C. Furthermore, if the spring or winter canola are cold acclimated the transformed plants may exhibit a further increase in freezing tolerance of at least −2° C.
To test salinity tolerance of the transformed plants, plants were watered with 150 mM NaCl. Plants overexpressing CBF1, CBF2 or CBF3 grew better compared with plants that had not been transformed with CBF1, CBF2 or CBF3.
22. Overexpression of CBF3 Affects Proline Metabolism
Proline levels in leaf samples were analyzed by methods described in Example 4.
Under non-cold acclimating growth conditions, the free proline levels in the CBF3-expressing plants were about 5-fold higher than they were in the control plants, levels which were about the same as those found in cold-acclimated control plants (
The proline biosynthetic enzyme Δ′-pyrroline-5-carboxylate synthase has a key role in determining proline levels in plants (Yoshiba et al. (1997) Plant Cell Physiol. 38, 1095-1102). Because of this, and that P5CS transcript levels have been shown to increase in Arabidopsis in response to low temperature (Xin and Browse (1998) Proc. Natl. Acad. Sci. USA 95, 7799-7804), it was of interest to determine whether P5CS transcript levels were elevated in the CBF3-expressing plants. Northern analysis indicated that they were; P5CS transcript levels were about 4 fold higher in non-cold acclimated CBF3-expressing plants than they were in non-cold acclimated control plants and were about equal to those found in the control plants that had been cold-treated for 1 day (
23. Overexpression of CBF3 Affects Sugar Metabolism
Total soluble sugars (e.g. sucrose, glucose, and fructose among others) were extracted from lyophilized leaf material as described in Example 4. The results showed that CBF3 expression affected the sugar levels in plants. Total soluble sugars in control and CBF3-expressing plants at both non-cold acclimating and cold acclimating temperatures were measured. The results show (
24. Overexpression of CBF3 Affects Lipid Composition
Total lipids were extracted from Arabidopsis leaves and measured as described in Example 4. The results indicated that CBF3 expression affected lipid composition. The representative results of Ws-2 and A28 are presented in
25. Overexpression of CBF3 Increases Arabidopsis Freezing Tolerance Whole Plant Freeze Test
Ws-2 and A30 seedlings were grown (13 days and 20 days, respectively) on Gamborg's B-5 medium containing 0.2% sucrose under sterile conditions in Petri dishes. The plants were tested for freezing tolerance by first placing the plates at −2° C. in the dark for 24 hours followed by ice nucleation with sterile ice chips for 3 hours. The temperature of the freezer was then turned down to −6° C. and the plates were left at this temperature for an additional 24 hours. The plates were taken from the freezer and placed at 4° C. in the dark for 18 hours, followed by 2 days at 22° C. under cool white fluorescent lights (40-50 μmol m−2 s−1) with an 18 hour photoperiod. The plates were scored 2 days later for freezing damage.
Electrolyte leakage freeze tests were performed essentially as described (Uemura et al. (1995) Plant Physiol. 109, 15-30.) with minor modifications. Tubes (16×125 mm) containing 3-4 leaves were placed in a low temperature bath set at −2° C. in a randomized design. The randomization was performed with the aid of the SAS system (SAS Institute Inc, Cary N.C.). Ice chips were added to each tube after 1 hour incubation. Each tube was capped with foam plugs and incubated a further 1 hour at −2° C. The bath temperature was then lowered one degree C. every 20 minutes. Tubes were removed at each temperature and incubated an additional hour at that same temperature in a separate bath. Tubes were placed on ice after removal from the bath until all tubes had been removed. The samples were then thawed overnight at 2.5° C. and electrolyte leakage was measured as described (Gilmour et al., 1988 Plant Physiol. 87, 745-750).
Non-cold acclimated control plants were killed by freezing at −6° C. for 24 hours while non-cold acclimated CBF3-expressing plants were not. Results for Ws-2 and A30 plants are shown in
While the present invention is disclosed by reference to the preferred embodiments and examples detailed above, it is to be understood that these examples are intended in an illustrative rather than limiting sense, as it is contemplated that modifications will readily occur to those skilled in the art, which modifications will be within the spirit of the invention and the scope of the appended claims.
This application is a continuation-in-part of the following U.S. applications: U.S. Application Ser. No. 09/580,377, filed: May 26, 2000, which in turn claimed priority from U.S. provisional Application Ser. No. 60/165,860, filed: Nov. 16, 1999, now abandoned; U.S. application Ser. No. 09/996,140, filed Nov. 26, 2001; U.S. application Ser. No. 09/601,802, filed: Sep. 15, 2000, which in turn claimed priority from PCT Application No.: PCT/US99/01895, filled: Jan. 28, 1999, now abandoned, which in turn claimed priority from U.S. application Ser. No. 09/198,119, filed: Nov. 23, 1998, which issued as U.S. Pat. No. 6,417,428; U.S. application Ser. No. 09/018,233, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/017,816, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/018,235, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/017,575, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/018,227, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/018,234, filed: Feb. 3, 1998, now abandoned; U.S. application Ser. No. 09/713,994, filed: Nov. 16, 2000, which in turn claimed priority from U.S. provisional Application Ser. No. 60/227,439 filed Aug. 22, 2000, now abandoned; and U.S. application Ser. No. 08/706,270, filed: Sep. 4, 1996, which issued as U.S. Pat. No. 5,892,009; each of which are incorporated herein by reference in their entirety.
This invention was supported by a subcontract under a USDA/CSREES Cooperative Agreement. The US Government has certain rights in this invention.
| Number | Date | Country | |
|---|---|---|---|
| 60165860 | Nov 1999 | US | |
| 60227439 | Aug 2000 | US | |
| 60166228 | Nov 1999 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 09580377 | May 2000 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09996140 | Nov 2001 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09601802 | Sep 2000 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | PCT/US99/01895 | Jan 1999 | US |
| Child | 09601802 | Sep 2000 | US |
| Parent | 09198119 | Nov 1998 | US |
| Child | PCT/US99/01895 | Jan 1999 | US |
| Parent | 09018233 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09197899 | Nov 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09017816 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09018235 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09017575 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09018227 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09018234 | Feb 1998 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 09713994 | Nov 2000 | US |
| Child | 10230415 | Aug 2002 | US |
| Parent | 08706270 | Sep 1996 | US |
| Child | 10230415 | Aug 2002 | US |
