Patent Application
20090158473
The present invention relates to nucleotide sequence capable of driving the expression of other nucleotide sequences.
An important consideration for the production of recombinant plants is the use of a gene promoter that exhibits appropriate activity in driving transgene expression. Promoters can control not only the level of gene expression, but also the timing and tissue specificity of expression.
There is interest in developing industrial oilseed crops that can be used to produce fatty acids having specific industrial utility. The castor plant (Ricinus communis) is of particular interest in this regard because of its long history of cultivation for castor oil. Therefore, promoters from castor for use in the production of transgenic varieties of castor and other plants would be an advancement in the art.
Example embodiments of the present invention include nucleotides sequences, vectors, cells, plants, and/or seeds comprising an isolated nucleotide sequence comprising a nucleotide sequence having at least about 90% homology to the sequence of SEQ ID NO:9 or SEQ ID NO:10.
Additional example embodiments of the present invention include nucleotides sequences, vectors, cells, plants, and/or seeds comprising a nucleotide sequence of interest operably linked to an isolated nucleotide sequence comprising a nucleotide sequence having at least about 90% homology to the sequence of SEQ ID NO:9 or SEQ ID NO:10.
A further example embodiment of the present invention comprises a method of promoting the expression of a molecule encoded by a nucleotide sequence of interest, the method comprising: operatively linking the isolated nucleotide sequence of claim 1 to the nucleotide sequence of interest.
An additional example embodiment of the present invention comprises a method of producing a molecule encoded by a nucleotide sequence of interest in a cell, the method comprising: operatively linking the isolated nucleotide sequence of claim 1 to the nucleotide sequence of interest; providing the operatively linked nucleotide sequences to the cell; and expressing the nucleotide sequence of interest.
An additional example embodiment of the present invention comprises a method of modulating the expression of a target in a cell, the method comprising: providing a nucleotide sequence of interest, wherein the nucleotide sequence encodes an antisense oligonucleotide or an siRNA that is capable of modulating the expression of the target in a cell; operatively linking the isolated nucleotide sequence of claim 1 to the nucleotide sequence of interest; providing the operatively linked nucleotide sequences to the cell; and expressing the nucleotide sequence of interest.
The present invention relates to nucleotide sequences capable of driving the expression of other nucleotide sequences. One aspect of the present invention provides an isolated nucleotide sequence that comprises a nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. In further aspects of the present invention, such a sequence is capable of acting as a promoter.
Further aspects of the present invention provide vectors comprising an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10.
Further aspects of the present invention provide cells comprising an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10.
Further aspects of the present invention provide cells comprising a vector comprising an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. As will be apparent to one of ordinary skill in the art, a cell can be any kind of cell capable of harboring a nucleotide sequence and/or a vector. Example of cells useful according to the present invention include, but are not limited to, eukaryotic cells, prokaryotic cells, animal cells, plant cells, bacterial cells, germ-line cells, seed cells, Arabidopsis sp. cells, sunflower cells, cotton cells, rapeseed cells, maize cells, palm cells, tobacco cells, peanut cells, soybean cells, and Ricinus sp. cells.
Further aspects of the present invention provide plants comprising an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. Examples of plants useful according to the present invention include, but are not limited to, sunflower, cotton, rapeseed, maize, palm, tobacco, peanut, soybean, Arabidopsis sp., and Ricinus sp.
Further aspects of the present invention provide seeds comprising an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. Examples of seeds useful according to the present invention include, but are not limited to, seeds from sunflower, cotton, rapeseed, maize, palm, tobacco, peanut, soybean, Arabidopsis sp., and Ricinus sp.
Further aspects of the present invention provide a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10.
Further aspects of the present invention provide vectors comprising a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10.
Further aspects of the present invention provide cells comprising a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10.
Further aspects of the present invention provide cells comprising a vector comprising a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. As will be apparent to one of ordinary skill in the art, a cell can be any kind of cell capable of harboring a nucleotide sequence. Example of cells useful according to the present invention include, but are not limited to, eukaryotic cells, prokaryotic cells, animal cells, plant cells, bacterial cells, germ-line cells, seed cells, sunflower cells, cotton cells, rapeseed cells, maize cells, palm cells, tobacco cells, peanut cells, soybean cells, Arabidopsis sp. cells, and Ricinus sp. cells.
Further aspects of the present invention provide plants comprising a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. Examples of plants useful according to the present invention include, but are not limited to, sunflower, cotton, rapeseed, maize, palm, tobacco, peanut, soybean, Arabidopsis sp., and Ricinus sp.
Further aspects of the present invention provide seeds comprising a nucleotide sequence of interest operatively linked to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10. Examples of seeds useful according to the present invention include, but are not limited to, seeds from sunflower, cotton, rapeseed, maize, palm, tobacco, peanut, soybean, Arabidopsis sp., and Ricinus sp.
As will be apparent to one of ordinary skill in the art, a nucleotide sequence of interest may be any nucleotide sequence that one wishes to express. Examples of nucleotides sequences of interest include, but are not limited to, nucleotide sequences encoding proteins, ribozymes, antisense RNAs, siRNAs, RNAi molecules, markers, reporters, enzymes, signaling molecules, proteins involved in fatty acid synthesis, degradation, storage, and/or regulation, antisense RNAs targeted to RNAs encoding proteins involved in fatty acid synthesis, degradation, storage, and/or regulation, and siRNAs and/or RNAi molecules targeted to RNAs encoding proteins involved in fatty acid synthesis, storage, degradation, and/or regulation.
Further aspects of the present invention provide methods of expressing a nucleotide sequence of interest. One example of such a method comprises operatively linking an nucleotide sequence of interest to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; and allowing the nucleotide sequence of interest to be expressed.
As will be apparent to one of ordinary skill in the art, allowing the nucleotide sequence of interest to be expressed relates generally to providing the operatively linked nucleotide sequences with or to an environment that allows for expression of the nucleotide sequence of interest. Examples of environments that allow for expression of the nucleotide sequence of interest are generally known in the art and include, but are not limited to, any environment having at least one dNTP and a polymerase, such as, but not limited to, an in vitro transcription kit, a PCR reaction, a cell, a eukaryotic cell, a prokaryotic cell, an animal cell, a plant cell, a bacterial cell, a germ-line cell, a seed cell, a sunflower cell, a cotton cell, a rapeseed cell, a maize cell, a palm cell, a tobacco cell, a peanut cell, a soybean cell, an Arabidopsis sp. cell, and a Ricinus sp. cell.
As will be appreciated by one of ordinary skill in the art, the operatively linked nucleotide sequences may be provided to an environment allowing expression using any procedure known in the art. Examples of such methods include, but are not limited to, transfection, using for example, lipofectin or lipofectamine, Agrobacterium mediated introduction (see, e.g., Chistou (1996), Trends Plant Sci., 1: 423-432; and Hooykaas and Schilperoot (1992), Plant Mol. Bio., 19: 15-38), floral dip (see, e.g., Clough and Bent (1998), Plant J., 16(6) 735-743), electroporation (see, e.g., Shigekawa and Dower (1988), Biotechniques, 6:742; Miller, et al. (1988), Proc. Natl. Acad. Sci. USA, 85:856-860; and Powell, et al. (1988), Appl. Environ. Microbiol., 54:655-660); direct DNA uptake mechanisms (see, e.g., Mandel and Higa (1 972), J. Mol. Biol., 53:159-162; Dityatkin, et al. (1972), Biochimica et Biophysica Acta, 281:319-323; Wigler, et al. (1979), Cell, 16:77; and Uchimiya, et al. (1982), In: Proc. 5th Intl. Cong. Plant Tissue and Cell Culture, A. Fujiwara (ed.), Jap. Assoc. for Plant Tissue Culture, Tokyo, pp. 507-508); fusion mechanisms (see, e.g., Uchidaz, et al. (1980), In: Introduction of Macromolecules Into Viable Mammalian Cells, Baserga et al. (eds.) Wistar Symposium Series, 1:169-185); infectious agents (see Fraley, et al. (1986), CRC Crit. Rev. Plant Sci., 4:1-46); and Anderson (1984), Science, 226:401-409); microinjection mechanisms (see, e.g., Crossway, et al. (1986), Mol. Gen. Genet., 202:179-185); and high velocity projectile mechanisms (see, e.g., EPO 0 405 696 to Miller, Schuchardt, Skokut and Gould, (The Dow Chemical Company).
Particular embodiments of the present invention provide methods of expressing a nucleotide sequence of interest in a seed preferred manner. One example of such a method comprises: operatively linking a nucleotide sequence of interest to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; directly or indirectly providing the operatively linked nucleotide sequences to a seed cell; and allowing for the expression of the nucleotide sequence of interest.
Other embodiments of the present invention provide methods of lowering the levels of a target protein. One example of such a method comprises: providing a nucleotide sequence encoding an antisense RNA and/or an siRNA that is capable of binding to an RNA encoding the target protein; operatively linking the nucleotide sequence encoding an antisense RNA and/or an siRNA to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; and allowing the nucleotide sequence encoding an antisense RNA and/or an siRNA to be expressed.
Other aspects of the present invention provide methods of lowering the levels of a target protein in a seed preferred manner. One example of such a method comprises: providing a nucleotide sequence encoding an antisense RNA and/or an siRNA that is capable of binding to an RNA encoding the target protein; operatively linking the nucleotide sequence encoding an antisense RNA and/or an siRNA to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; directly or indirectly providing the operatively linked nucleotide sequences to a seed cell; and allowing the nucleotide sequence encoding an antisense RNA and/or an siRNA to be expressed.
Further aspects of the present invention provide methods of changing the fatty acid content of a seed. One example of such a method comprises: operatively linking a nucleotide sequence encoding a protein involved in fatty acid synthesis, degradation, storage, and/or regulation to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; directly or indirectly providing the operatively linked nucleotide sequences to a seed cell; and allowing for the expression of the nucleotide sequence of interest. Examples of proteins involved in fatty acid synthesis, degradation, storage, and/or regulation include, but are not limited to, ACCase, FAS, KAS I, KAS II, KAS III, Fad2, and Fad3.
An additional example of a method of changing the fatty acid content of a seed comprises: providing a nucleotide sequence encoding an antisense RNA and/or an siRNA that is capable of binding to an RNA encoding a protein involved in fatty acid synthesis, degradation, storage, and/or regulation; operatively linking the nucleotide sequence encoding an antisense RNA and/or an siRNA to an isolated nucleotide sequence having at least about 60% identity, at least about 70% identity, at least about 80% identity, at least about 90% identity, or at least about 95% identity to a nucleotide sequence selected from SEQ ID NO:9 and SEQ ID NO:10; directly or indirectly providing the operatively linked nucleotide sequences to a seed cell; and allowing the nucleotide sequence encoding an antisense RNA and/or an siRNA to be expressed.
As used herein, a “promoter” refers to a region of DNA, generally upstream from the transcription initiation site, which is involved in recognition and binding of RNA polymerase and other proteins to initiate transcription. A promoter may include enhancers and repressors.
As used herein, “operably linked” refers to nucleotides sequences being joined so as to function in their intended manner. Sequences that are “operatively linked” may or may not be directly contiguous. For example, a promoter which is operatively linked to a nucleotide sequence of interest can be joined and positioned in such a way that it is capable of driving the expression of the nucleotide sequence of interest.
The present invention is further described in the following examples, which are offered by way of illustration and are not intended to limit the invention in any manner.
Genes encoding the legumin-like (“54-SSP”) and oleosin proteins were identified via a random cDNA sequencing project, wherein gene annotation was accomplished using sequence-based homology to known genes. The promoters for these selected genes were isolated via PCR-based “genome walking,” using a GenomeWalker™ kit (Clontech Laboratories, Inc.) according to the manufacturer's instructions. In this technique, short oligonucleotide adapter molecules with a known sequence were first ligated onto the ends of castor genomic DNA that had been digested with several different blunt-cutting restriction enzymes. A primary PCR reaction was carried out using a forward PCR primer that annealed to the adapter molecule and a reverse PCR primer that annealed specifically to the DNA within the coding region of the 54-SSP or oleosin gene. A second round of PCR using nested primers, also based on the known adapter and gene-specific sequences, was then carried out. Using this strategy, DNA sequences upstream from the selected coding sequences were isolated and inserted into the cloning vector pCR2.1 (Invitrogen Corp.) and sequenced. The primers used in this process are shown below.
Once the sequences of the promoter fragments obtained in this manner were determined, it was possible to generate additional PCR products with specific cloning sites built into the primer sequences to facilitate expression vector construction.
The consensus nucleotide sequence of the 54-SSP promoter (1124 base pairs immediately preceding the 54-SSP start codon) can be found at SEQ ID NO:9.
The consensus nucleotide sequence of the oleosin promoter (528 base pairs immediately preceding the oleosin start codon) can be found at SEQ ID NO:10. It should be noted that the clone used for oleosin promoter testing had a PCR-generated sequence error, wherein the T at position 234 was replaced by an A.
The activities of the oleosin and 54-SSP gene promoters were tested in whole plants (Arabidopsis thaliana) through the use of the reporter gene Green Fluorescent Protein (GFP). Binary vectors for Arabidopsis transformation were constructed that had an expression cassette with the oleosin or 54-SSP promoter upstream of the CopGFP gene (Evrogen), followed by a Cauliflower Mosaic Virus 35S terminator region. Maps for the following vectors are shown in
Arabidopsis plants were transformed by the floral dip method (Clough and Bent Plant Journal 16:735-743). The binary vectors contained the phosphinothricin acetyltransferase (PAT) gene, which allowed selection of transformants on the herbicide glufosinate. In order to determine whether the promoters were active primarily in seeds, certain tissues were harvested from first generation (T1) transformants, including leaves, developing siliques, and mature seeds. These tissues were tested for CopGFP fluorescence as described below. The seeds from the TI plants were planted to generate T2 plants, from which leaf, developing siliques, and mature seed samples were also taken and analyzed. Tissue samples were analyzed by the following CopGFP Assay procedure:
CopGFP Assay: Tissue samples were ground in 1×CCLR buffer (Cell Culture Lysis Buffer 5× Reagent (Promega Corp., catalog #E153A) containing 125 mM Tris (pH 7.8) with H3PO4, 10 mM CDTA, 10 mM DTT, 50% glycerol and 5% Triton X-100) for one minute in a tissue homogenizer. Samples were placed on dry ice until further use. The extracts were centrifuged at 14K×g for 15 minutes at 4° C. The supernatant fluid was transferred into another tube and used for further analysis. 200 μl of each supernatant was placed in a Costar 96-well flat bottom microtiter plate (Coming, Inc., catalog #3915) and fluorescence was measured using a SpectraMax Gemini XS microplate reader (Molecular Devices, Inc.). A culture containing an E. coli strain expressing CopGFP was used as a standard. The protein concentration of the tissue extracts was determined with a BCA protein assay kit (Pierce Biotechnology, Inc.; catalog #23225). Fluorescence was expressed as fluorescence per mg of protein. All experiments were performed in duplicate.
The results of these studies are presented in
Additional testing of the oleosin promoter was carried out in Arabidopsis plants using the luciferase gene as a reporter gene. The results of these experiments also indicated higher activity of the oleosin promoter in seeds.
Vectors for the modulation of fatty acid synthesis proteins are created as outlined in Example 2. The following vectors encoding fatty acid synthesis proteins under the control of the 54-SSP promoter are created:
The following vectors encoding fatty acid synthesis proteins under the control of the Oleosin promoter are created:
pOleo:KASII—Oelosin promoter operatively linked to a KASII gene.
The following vectors encoding antisense molecules against fatty acid synthesis proteins under the control of the 54-SSP promoter are created:
The following vectors encoding antisense molecules against fatty acid synthesis proteins under the control of the Oleosin promoter are created:
Vectors encoding siRNA molecules against fatty acid synthesis proteins are created. The siRNA molecules may be designed to express an RNA molecule that hybridizes with itself to form a hairpin structure that comprises a single-stranded loop region and a base-paired stem. The base-paired stem region comprises a sense sequence corresponding to all or part of the endogenous messenger RNA encoding the gene whose expression is to be inhibited, and an antisense sequence that is fully or partially complementary to the sense sequence. Thus, the base-paired stem region of the molecule generally determines the specificity of the RNA interference. These hairpin RNA molecules are highly efficient at inhibiting the expression of endogenous genes, and the RNA interference they induce is inherited by subsequent generations. See, for example, Chuang and Meyerowitz (2000) Proc. Natl. Acad. Sci. USA 97:5985-5990; Stoutjesdijk et al. (2002) Plant Physiol. 129:1723-1731; and Waterhouse and Helliwell (2003) Nat. Rev. Genet. 5:29-38. Methods for using hpRNA interference to inhibit or silence the expression of genes are described, for example, in Chuang and Meyerowitz (2000) Proc. Natl. Acad. Sci. USA 97:5985-5990; Stoutjesdijk et al. (2002) Plant Physiol. 129:1723-1731; Waterhouse and Helliwell (2003) Nat. Rev. Genet. 5:29-38; Pandolfini et al. BMC Biotechnology 3:7, and U.S. Patent Publication No. 20030175965. A transient assay for the efficiency of hairpin RNA constructs to silence gene expression in vivo has been described by Panstruga et al. (2003) Mol. Biol. Rep. 30:135-150.
The following vectors encoding siRNA molecules against fatty acid synthesis proteins under the control of the 54-SSP promoter are created:
The following vectors encoding antisense molecules against fatty acid synthesis proteins under the control of the Oleosin promoter are created:
Arabidopsis and Ricinus are cultivated under normal conditions. The vectors are introduced into Agrobacterium tumefaciens strain GV3 101 pMP90 by electroporation and used to transform Arabidopsis thaliana and Ricinus communis plants by the floral dip method (N. Bechtold, J. Ellis, and G. Pelletier (1993) C. R. Acad. Sci. Paris 316, 1194-1198). Vectors are also introduced using high velocity particles and infectious agents Transformation is performed ˜5 days after initial flowering.
Fatty Acid Analysis: Seeds are methylated (1 ml of 1 N HCl, methanol, Supelco, 80° C. for one hour), and extracted with hexane and trimethylsilylated (100 μl of BSTFA-TMCS (bis(treimethylsilyl)trifluoroacetamidetrimethylsilane), Supelco, 90° C. for 45 minutes). The BSTFA-TMCS is removed by evaporation and the sample is resuspended in hexane. Samples are analyzed on a Hewlett-Packard 6890 gas chromatograph equipped with a 5973 mass selective detector (GC/MS) and a Supelco SP-2340 cyano capillary column (60 m×250 μm×0.25 μm). The injector is held at 225° C., the oven temperature is varied (100-240° C. at 15° C./minute followed by 240° C. for five minutes), and the helium flow is 1.1 ml/minute. Assignment of peak identities is performed based on elution time versus authentic standards and validated based on their mass spectra. Quantitation is performed using Hewlett-Packard chemstation software.
Three methods of modulating fatty acid synthesis via Fad2 are compared (gene expression, antisense expression, siRNA expression). Three genes are chosen for the comparison of the three methods of gene repression (the 12-desatuarse FAD2 and the 15-desaturase FAD3 because they are easily scored; and the FAD2 because it had been used before for evaluation of reduction in gene expression), as well as β-ketoacyl-ACP synthase (KAS) II. The relationship between these enzymes and fatty acid synthesis is depicted in
Seeds are chosen for analysis because they allow for reproducible quantitative analysis of their composition by gas chromatography and because they allow for mass spectrometric analysis of peaks to qualitatively confirm the assignments of peaks as specific fatty acids. Student T-test is used to assign significance to differences between means (based on ten or more samples per mean).
KASII elongates 16 C to 18 C fatty acids in the plastid. For KASII, levels of 16:0 plus 16:1 fatty acids (the substrates for KASII) are compared with the levels of its product 18:0 and 18:1 plus metabolites 18:2 and 18:3.
Wild-type Arabidopsis and Ricinus are compared to lines transformed with pSSP:KASII, pOleo:KASII, pSSP:KASII:AS, pOleo:KASII:AS, pSSP:KASII:si, or pOleo:KASII:si. Those plants harboring the pSSP:KASII and pOleo:KASII vectors show significant decreases in 16:0 fatty acids with corresponding increases in C18 and higher fatty acids. Those plants harboring the pSSP:KASII:AS, pOleo:KASII:AS, pSSP:KASII:si, and pOleo:KASII:si vectors show significant increases in 16:0 fatty acids with corresponding decreases in C18 and higher fatty acids.
For FAD2, levels of 18:1 fatty acids (the substrate for FAD2) are compared with the levels of its product 18:2 and the metabolite 18:3. For analysis, 18:2 is summed with 18:3 to get the total fatty acid proportion that had been desaturated by FAD2.
Wild-type Arabidopsis and Ricinus are compared to lines transformed with pSSP:FAD2, pOleo:FAD2, pSSP:FAD2:AS, pOleo:FAD2:AS, pSSP:FAD2:si, or pOleo:FAD2:si. Those plants harboring the pSSP:FAD2 and pOleo:FAD2 vectors show significant increases in 18:2 and 18:3 fatty acids. Those plants harboring the pSSP:FAD2:AS, pOleo:FAD2:AS, pSSP:FAD2:si, and pOleo:FAD2:si vectors show significant decreases in 18:2 and 18:3 fatty acids with corresponding increases in lower order fatty acids.
For FAD3, levels of 18:1 plus 18:2 fatty acids (18:2 being the substrate for FAD3) are compared with the levels of its product 18:3.
Wild-type Arabidopsis and Ricinus are compared to lines transformed with pSSP:FAD3, pOleo:FAD3, pSSP:FAD3:AS, pOleo:FAD3:AS, pSSP:FAD3:si, or pOleo:FAD3:si. Those plants harboring the pSSP:FAD3 and pOleo:FAD3 vectors show significant increases in 18:3 fatty acids. Those plants harboring the pSSP:FAD3:AS, pOleo:FAD3:AS, pSSP:FAD3:si, and pOleo:FAD3:si vectors show significant decreases in 18:3 fatty acids with corresponding increases in lower order fatty acids.
While this invention has been described in certain example embodiments, the present invention may be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fall within the limits of the appended claims.
All references, including publications, patents, and patent applications, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
This application is a utility conversion of U.S. Provisional Patent Application Ser. No. 60/992,273, filed Dec. 4, 2007, for “Seed-Preferred Gene Promoters From the Castor Plant.”
Work described herein was supported in part by an award from the Department of Energy; award number DE-FC07-01ID 14213. The United States Government may have certain rights in the invention.
| Number | Date | Country | |
|---|---|---|---|
| 60992273 | Dec 2007 | US |
