METHOD FOR PRODUCING STRESS TOLERANT TRANSGENIC PLANT BY SILENCING A GENE ENCODING CALCIUM-DEPENDENT LIPID-BINDING PROTEIN WITH C2 DOMAIN AND APPLICATIONS OF THE SAME

Abstract

A transgenic plant includes a first gene having a first polynucleotide and a recombinant construct having a second polynucleotide. The first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1. The first polynucleotide encodes a C2-like domain, and the Atclb gene fragment encodes a C2 domain represented by amino acids 265-345 of SEQ ID NO:2. The C2-like domain is homologous to the C2 domain. The second polynucleotide has at least 90% identity to the first polynucleotide or a sequence complimentary to the first polynucleotide. The recombinant construct is configured to silence the first gene such that the transgenic plant is tolerant to abiotic stress. A method to produce the transgenic plants.

Description

FIELD OF THE INVENTION

The present invention relates generally to a method for producing a transgenic plant and application of same, and more particularly to a method for increasing stress tolerance of a plant by silencing a gene encoding calcium-dependent lipid-binding protein with C2 domain and a plant produced thereof.

BACKGROUND OF THE INVENTION

All abiotic stresses (cold, drought, salt) reduce plant growth and yield. These are the major limiting factors in agricultural productivity and quality, thus preventing crop plants from realizing their full genetic potential.

Transgenic or recombinant plants are of increasing interest because of the potential to control phenotypic traits as well as to produce large quantities of commercially useful products. Plants have been employed to overproduce heterologous proteins and in principle can produce a wide range of products, including high value proteins and certain pharmaceuticals. Transgenic plants with enhanced production traits such as the ability to survive and thrive after exposure to prolonged environmental stress are particularly desirable as a source of economic benefit to the commercial agricultural plant community including horticulturists, food producers, and agronomist. The identification of new genes that can effectively control stress response in plants is one of the major goals of plant biotechnology. Unfortunately, in many cases overexpression of genes involved in stress signaling can lead to morphological abnormalities, restricting the potential for use in commercial production.

Therefore, a heretofore unaddressed need exists in the art to address the aforementioned deficiencies and inadequacies.

SUMMARY OF THE INVENTION

In one aspect, the present invention is directed to a transgenic plant.

In one embodiment, the transgenic plant includes a first gene having a first polynucleotide and a recombinant construct having a second polynucleotide. The first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1. The second polynucleotide has at least 90% identity to the first polynucleotide or a sequence complimentary to the first polynucleotide. The recombinant construct is configured to silence the first gene such that the transgenic plant is tolerant to abiotic stress.

In one embodiment, the first polynucleotide has at least 50% similarity to the Atclb gene fragment.

In one embodiment, the first polynucleotide encodes a C2-like domain, and the C-2 like domain has at least 50% amino acid identity to amino acids 265-345 of SEQ ID NO: 2.

In one embodiment, the second polynucleotide is substantially identical to the first polynucleotide or the sequence complimentary to the first polynucleotide.

In one embodiment, the recombinant construct is configured to silence the first gene of the transgenic plant by RNA interference, anti-sense construction or virus induced gene silencing (VIGS).

In one embodiment, the abiotic stress is water deficit, salt stress, cold stress or a combination thereof.

In one embodiment, the transgenic plant is formed from a plant of Solanum lycopersicum, Ricinus communis, Populus trichocarpa, Vitis vinifera, Oryza sativa, or Sorghum bicolor, and the identified genes are SlCLB1, RcCLBP, PtIMSCDP, VvHP, OsHP, or SbIMSCDP, respectively.

In one embodiment, the transgenic plant is formed from the Oryza sativa, and the first gene is OsHP gene encoding Oryza sativa histidine-containing phosphotransfer protein.

In one embodiment, the transgenic plant is formed from the Solanum lycopersicum, and the first gene is SlCLB1 gene encoding a protein with a Ca²⁺-dependent lipid-binding domain.

In one embodiment, a seed is produced by the transgenic plant.

In another aspect, the present invention is directed to a transgenic plant. The transgenic plant includes a mutated first gene such that the transgenic plant is tolerant to abiotic stress. The first gene to be mutated has a first polynucleotide. The first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1.

In yet another aspect, the present invention is directed to a method of producing transformed plant cells.

In one embodiment, the method includes: identifying a first gene of plant cells; constructing a recombinant construct for silencing the first gene in the plant cells; and transforming the plant cells with the recombinant construct to form the transformed plant cells. The first gene in the transformed plant cell is silenced by the recombinant construct such that the plant cells are tolerant to an abiotic stress. The first gene includes a first polynucleotide, and the first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1. The recombinant construct includes a second polynucleotide, and the second polynucleotide has at least 90% similarity to the first polynucleotide or a sequence complimentary to the first polynucleotide.

In one embodiment, the method further includes confirming the silencing of the first gene in the transformed plant cells.

In one embodiment, the method further includes producing a plant from the transformed plant cells.

In one embodiment, the first polynucleotide has at least 50% similarity to the Atclb gene fragment.

In one embodiment, the first polynucleotide encodes a C2-like domain, and the C-2 like domain has at least 50% amino acid identity to amino acids 265-345 of SEQ ID NO: 2.

In one embodiment, the second polynucleotide is substantially identical to the first polynucleotide or the sequence complimentary to the first polynucleotide.

In one embodiment, the plant cells are Solanum lycopersicum cells, Ricinus communis cells, Populus trichocarpa cells, Vitis vinifera cells, Oryza sativa cells, or Sorghum bicolor cells.

In one embodiment, the plant cells are the Oryza sativa cells, and the first gene is OsHP gene encoding Oryza sativa histidine-containing phosphotransfer protein.

In one embodiment, the plant cells are the Solanum lycopersicum cells, and the first gene is SlCLB1 gene encoding a protein with a Ca²⁺-dependent lipid-binding domain.

In one embodiment, the recombinant construct is configured to silence the first gene of the plant cells by RNA interference, anti-sense construction or virus induced gene silencing (VIGS).

In one embodiment, the abiotic stress is water deficit, salt stress, cold stress or a combination thereof.

In one embodiment, the plant cells are transformed by agrobacterial transformation or bombardment transformation to form the transformed plant cells.

In one aspect, the present invention is directed to a transgenic plant produced from the transformed plant cells.

In one aspect, the present invention is directed to a seed produced by the transgenic plant.

In a further aspect, the present invention is directed to a method of producing transformed plant cells.

In one embodiment, the method includes mutating a first gene of plant cells to form the transformed plant cells such that the transformed plant cells are tolerant to an abiotic stress. A first polynucleotide of the first gene is homologous to Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1.

These and other aspects of the present invention will become apparent from the following description of the preferred embodiment taken in conjunction with the following drawings, although variations and modifications therein may be effected without departing from the spirit and scope of the novel concepts of the disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings illustrate one or more embodiments of the invention and, together with the written description, serve to explain the principles of the invention. Wherever possible, the same reference numbers are used throughout the drawings to refer to the same or like elements of an embodiment.

FIG. 1 illustrates a method for producing a plant tolerant to stress conditions by silencing a gene in the plant that is homologous to Arabidopsis thaliana Atclb gene, according to one embodiment of the present invention.

FIG. 2A illustrate the schematic structure of the AtCLB protein, according to one embodiment of the present invention.

FIG. 2B illustrate the amino acid sequence alignment of C2 domain of the AtCLB protein with its homologues from different plant species, according to one embodiment of the present invention.

FIG. 2C illustrate phylogenetic analysis of the C2 domains from the different plant species, according to one embodiment of the present invention;.

FIGS. 3A-3E illustrate drought-tolerance phenotype of T-DNA insertion knockout lines Atclb1-1 and Atclb1-2 produced according to one embodiment of the present invention.

FIG. 3A is a schematic diagram of AtCLB genomic structure and T-DNA insertion site in the mutant allele Atclb1, according to one embodiment of the present invention.

FIG. 3B illustrate germination rate of Arabidopsis thaliana wild type (WT), a line expressing Atclb under the control of the 35S promoter, and two knockout mutant lines after 1 week of incubation on Murashige and Skoog medium (MS medium), according to one embodiment of the present invention.

FIG. 3C illustrate phenotype of wild type (WT) and knockout mutant lines after 3 weeks of withholding water, according to one embodiment of the present invention.

FIG. 3D illustrate relative leaf water content of 4-week-old wild type (WT) and two knockout mutant lines during 3 weeks of water deficit stress, according to one embodiment of the present invention.

FIG. 3E illustrate expression analysis of wild type and two homozygous knockout lines (Atclb1-1 and Atclb1-2 of thaliana) by RT-PCR, according to one embodiment of the present invention.

FIGS. 4A-4C illustrate salt-tolerance phenotype of T-DNA insertion knockout lines Atclb1-1 and Atclb1-2 produced according to one embodiment of the present invention.

FIG. 4A illustrate germination of Arabidopsis thaliana wild type (WT) and Atclb1-1 line in the presence of 150 millimolar (mM) sodium chloride (NaCl), according to one embodiment of the present invention.

FIG. 4B illustrate seedings of loss-of-function Atclb1-1 mutant line were able to survive in the presence of 150 mM NaCl, according to one embodiment of the present invention.

FIG. 4C illustrate one-week-old Arabidopsis thaliana seedlings with 10 to 20 millimeter (mm) long roots on vertical agar plates were transferred to plates supplemented with NaCl and allowed to grow vertically at 23° C. with a 16-h light period, according to one embodiment of the present invention.

FIG. 5 illustrates a method for producing a rice plant tolerant to stress conditions by silencing a gene from rice plant that is homologous to Arabidopsis thaliana Atclb gene, according to one embodiment of the present invention.

FIG. 6 illustrates a method for producing a tomato plant tolerant to stress conditions by silencing a gene from tomato plant that is homologous to Arabidopsis thaliana Atclb gene, according to one embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention will now be described more fully hereinafter with reference to the accompanying drawings, in which exemplary embodiments of the invention are shown. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this invention will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. Like reference numerals refer to like elements throughout.

As used in the description herein and throughout the claims that follow, the meaning of “a,” “an,” and “the” includes plural reference unless the context clearly dictates otherwise. Also, as used in the description herein and throughout the claims that follow, the meaning of “in” includes “in” and “on” unless the context clearly dictates otherwise. Moreover, titles or subtitles may be used in the specification for the convenience of a reader, which has no influence on the scope of the invention. Additionally, some terms used in this specification are more specifically defined below.

As used herein, the terms “comprise or comprising”, “include or including”, “have or having”, “contain or containing” and the like are to be understood to be open-ended, i.e., to mean including but not limited to.

Typically, terms such as “first”, “second”, “third”, and the like are used for distinguishing various elements, members, regions, layers, and areas from others. Therefore, the terms such as “first”, “second”, “third”, and the like do not limit the number of the elements, members, regions, layers, areas, or the like. Further, for example, the term “first” can be replaced with the term “second”, “third”, or the like.

Typically, terms such as “about,” “approximately,” “generally,” “substantially,” and the like unless otherwise indicated mean within 20 percent, preferably within 10 percent, preferably within 5 percent, and even more preferably within 3 percent of a given value or range. Numerical quantities given herein are approximate, meaning that the term “about,” “approximately,” “generally,” or “substantially” can be inferred if not expressly stated.

As used herein, “AtCLB” refers to a Ca²⁺-dependent lipid-binding protein from Arabidopsis thaliana encoded by Atclb gene of Arabidopsis thaliana. AtCLB contains a Ca²⁺-binding domain or C2 domain. AtCLB may be a transcriptional regulator in the Ca²⁺ signaling pathway.

As used herein, an “Atclb gene” from Arabidopsis thaliana encodes the protein AtCLB. Atclb gene is identified as a novel and negative regulator for stress tolerance that can negatively regulate response to abiotic stress in Arabidopsis thaliana.

A protein “homologous” to AtCLB protein may have at least 30% identical or conserved amino acid sequence in comparison to AtCLB protein sequence. Preferably, the sequence identity or similarity between the homologous protein sequence and AtCLB protein sequence is more than 60%. More preferably, the sequence identity or similarity between the homologous protein sequence and AtCLB protein sequence is more than 90%. Further, the sequence identity or similarity between the homologous protein sequence and AtCLB protein sequence is more than 95%.

The description will be made as to the embodiments of the present invention in conjunction with the accompanying drawings in FIGS. 1-6. In accordance with the purposes of this invention, as embodied and broadly described herein, this invention, in one aspect, relates to method for producing transgenic plant.

In one aspect the present invention, a method for increasing plant productivity by enhancement of tolerance to stressful environmental conditions, especially abiotic stress including water deficit stress, cold and salt stress is provided. The method includes applying genetic approach and silencing key genes involved in plant stress signaling.

Mutation in Arabidopsis thaliana Atclb gene encoding calcium-dependent protein with a C2 domain (AtCLB) leads to significant increase of abiotic stress tolerance in Arabidopsis thaliana plant. Thus, lack of expression of Atclb gene with following lack of production of AtCLB protein leads to increase of tolerance to water deficit and salt stresses in Atclb mutants of Arabidopsis thaliana.

Many valuable crops have homologues of Atclb gene. Bioinformatics analysis revealed genes from important crops including tomato and rice, which include sequences identical/similar to Atclb gene fragment encoding C2 domain. Increasing crop tolerance to stressful environmental conditions in valuable crops may be achieved by silencing of those genes homologues to Atclb gene.

In one embodiment, the plant is Solanum lycopersicum, and the gene homologous to Atclb gene is SlCLB1, the plant is Ricinus communis, and the gene homologous to Atclb gene is RcCLBP, the plant is Populus trichocarpa, and the gene homologous to Atclb gene is PtIMSCDP, the plant is Vitis vinifera, and the gene homologous to Atclb gene is VvHP, the plant is Oryza sativa, and the gene homologous to Atclb gene is OsHP, or the plant is Sorghum bicolor, and the gene homologous to Atclb gene is SbIMSCDP.

In one embodiment, rice has the OsHP gene encoding Oryza sativa histidine-containing phosphotransfer protein. The OsHP gene is homologous to Atclb gene. Transformation of rice with an established vector construction (for example, Panda-OsHP) may silence rice OsHP gene and increase stress tolerance of a transformed rice plant.

Genetically modified plants carrying silenced homolog of Atclb gene can be used as alternative to traditional crops in areas with stressful environmental conditions (areas with water deficit, areas with salt soil). The production of those transgenic crops, among other things, will enhance productivity of lands and benefit agriculture.

FIG. 1 illustrates a method for producing a plant tolerant to stress conditions by silencing a gene in the plant that is homologous to Arabidopsis thaliana Atclb gene, according to one embodiment of the present invention. The stress may be abiotic stress and includes water deficit, salt stress, cold stress or a combination thereof. The method includes the following steps.

In step 101, a gene homologues to Atclb gene is identified from a plant or crop of choice. In one embodiment, the gene from the plant or crop of choice is identified by bioinformatics analysis. In certain embodiments, the gene has a first polypeptide encoding a C2-like domain. The first polypeptide of the gene is homologous to a fragment of the Atclb gene that encoding C2 domain of the ATCLB protein. The nucleotide fragment encoding C-2 domain of ATCLB protein is represented by nucleotide acids 963-1205 of SEQ ID NO:1, and the C-2 domain of ATCLB protein is represented by amino acids 265-345 of SEQ ID NO:2. The first polynucleotide is homologous to the nucleotide acids 963-1205 of SEQ ID NO:1, and the C2-like domain encoded by the first polynucleotide is homologous to the C2 domain, i.e., amino acids 265-345 of SEQ ID NO:2.

In certain embodiments, the first polynucleotide from the plant of choice has at least about 30% sequence similarity to the Atclb gene fragment encoding C 2 domain. Preferably, the sequence similarity is above 50%. More preferably, the sequence similarity/identity is above 90%.

In certain embodiments, the first polynucleotide from the plant of choice has at least about 30% sequence identity to the Atclb gene fragment encoding C 2 domain. Preferably, the sequence identity is above 50%. More preferably, the sequence identity is above 90%. In certain embodiments, due to the gene degeneracy, the protein pairwise identity percentage is higher than the corresponding nucleic acid pairwise identity percentage.

In certain embodiments, the C2-like domain from the plant of choice has at least about 30% sequence similarity to the C2 domain of AtCLB protein. Preferably, the sequence similarity is above 50%. More preferably, the sequence similarity/identity is above 90%.

In certain embodiments, the C2-like domain from the plant of choice has at least about 30% sequence identity to the C2 domain of AtCLB protein. Preferably, the sequence identity is above 50%. More preferably, the sequence identity is above 90%. In certain embodiments, due to the gene degeneracy, the protein pairwise identity percentage is higher than the corresponding nucleic acid pairwise identity percentage.

Bioinformatics analysis has revealed that the C2 domain of Arabidopsis thaliana calcium-dependent, lipid-binding protein is homologous to the C2-like domain sequences of important crops, including tomato and rice. Expression analysis of Atclb rice homologue (OsHP) confirmed the presence of the gene transcripts in root, stem, leaf, flower of these crops (data generated but not shown here). T-DNA knockout mutant analysis revealed that down regulation of AtCLB containing a conserved C2 domain could confer resistance to various abiotic stress conditions such as salinity and drought in Arabidopsis thaliana (FIGS. 2 and 3). Silencing of the expression of AtCLB C2 domain homologues in crops proves involvement of conserved C2 domain in stress signaling and potentially brings resistance to abiotic stress conditions.

AtCLB gene was identified using a 240-bp DNA sequence as bait in a yeast one-hybrid screen assay against the cDNA library from Arabidopsis thaliana root apices. The 240-bp DNA sequence is a fragment of the promoter region of AtTHAS1 (Thalianol synthase). The identified AtCLB gene codes for an Arabidopsis thaliana calcium-dependent lipid-binding protein (AtCLB) with a C2-like domain. Referring to FIG. 2A, AtCLB is a putative C2-domain-like protein containing 510 amino acid residues with a predicted molecular mass of 55 kDa, represented by SEQ ID NO2. The AtCLB protein has a predicted N-terminal signal peptide at positions 1-22, a predicted C-terminal coiled-coil region, and the C2 domain at positions 265-345. The asterisks in the C2 domain represents four of the five conserved aspartic acid residues at positions 285, 333, 335, and 339 that are thought to be involved in Ca²⁺ binding.

Referring to FIG. 2B, identical residues in all sequences in the alignment are denoted by ‘*’ while conserved substitutions and semi-conserved substitutions are denoted by ‘:’ and ‘.’ respectively. BLAST analysis revealed that the C2 domain of AtCLB protein has significant homology to C2-domain sequences from plant species SlCLB1 gene of plant Solanum lycopersicum, RcCLBP gene of plant Ricinus communis, PtIMSCDP gene of plant Populus trichocarpa, VvHP gene of plant Vitis vinifera, OsHP gene of plant Oryza sativa, and SbIMSCDP gene of plant Sorghum bicolor. The pairwise identities of AtCLB protein with its homologous C2-domain sequences SlCLB1, RcCLBP, PtIMSCDP, VvHP, OsHP, and SbIMSCDP proteins are >57%.

Referring to FIG. 2C, to evaluate the divergence of the C2 domain of AtCLB from other C2 domains aligned in FIG. 2B, a phylogenetic tree was constructed using C2-domain sequences of these proteins and it was found that they fall into distinct classes, with AtCLB sharing the same group as SlCLB1. The length of lines connecting the different C2 domains is a measure of their sequence distance.

In step 103, a recombinant construct, such as a vector, is constructed. The recombinant construct comprises a second polynucleotide. In certain embodiment, the second polynucleotide has at least 90% sequence identity to the first polynucleotide or a sequence complimentary to the first polynucleotide. In one embodiment, the second polynucleotide is identical to the first polynucleotide. In one embodiment, the second polynucleotide is identical to the complementary sequence of the first polynucleotide. The recombinant construct is capable of switching off (silencing) the gene in the plant that is homologous to Atclb gene. In one embodiment, the recombinant construct is constructed for RNA silencing, antisense silencing or virus induced gene silencing (VIGS).

In step 105, the plant is transformed with the established recombinant construct by any available transformation technique. In certain embodiments, the transformation method may include agrobacterial transformation and bombardment method.

In certain embodiments, the transformation of the plant has a transient silencing effect. In certain preferred embodiments, the transformation of the plant has a stable silencing effect that can be passed on.

The method may further include a confirmation step to confirm or select transgenic plants with the gene homologous to Atclb gene successfully silenced. In one embodiment, homozygous lines of transgenic plants are tested in abiotic stress experiments and stress tolerant lines can be selected for range of field experiments.

EXAMPLE 1

Tolerance to Water of Arabidopsis thaliana with Mutated Atclb Gene

An Arabidopsis thaliana Ca²⁺-dependent lipid-binding protein (AtCLB) containing C2 domain is able to negatively regulate stress response in Arabidopsis thaliana. Expression of the Atclb gene was documented in all analyzed tissues of Arabidopsis thaliana (leaf, root, stem, flower, and silique) by real-time PCR analysis. Immunofluorescence analysis revealed that AtCLB protein is localized in the nucleus of cells in Arabidopsis thaliana root tips. It is demonstrated that the AtCLB protein is capable of binding to the membrane lipid ceramide. The role of the Atclb gene in negatively regulating responses to abiotic stress in Arabidopsis thaliana was identified. FIGS. 3A-3E illustrate drought-tolerance phenotype of T-DNA insertion knockout lines Atclb1-1 and Atclb1-2 produced according to one embodiment of the present invention.

Two T-DNA insertion knockout mutant lines Atclb1-1 and Atclb1-2 were constructed. The mutant lines Atclb1-1 and Atclb1-2 were confirmed homozygous mutant lines. FIG. 3A shows schematically the AtCLB genomic structure, with T-DNA insertion site indicated for Atclb-1. Referring to FIG. 3A, 5′UTR and 3′UTR are 5′ untranslated region and 3′ untranslated region respectively. The start codon ATG and stop codon TGA are labeled. The box and solid lines indicate exons and introns, respectively, and E1-E11 represent 11 exons. The insertion position of the T-DNA in the Atclb1-1 mutant line is indicated by a triangle, which pointed to exon 10.

FIG. 3E shows expression analysis of wild type and two homozygous knockout lines Atlcb1-1 and Atclb1-2 of Arabidopsis thaliana by reverse transcription polymerase chain reaction (RT-PCR). Actin was used as the internal control. As shown in FIG. 3E, transcript of the Atclb gene was detected in the wild type (WT) Arabidopsis thaliana, while no transcript of the Atclb gene was detected in either of the knockout lines Atlcb1-1 and Atclb1-2.

Referring to FIG. 3B, germination rate of Arabidopsis thaliana wild type (WT), a line expressing Atclb under the control of the 35S promoter, and two knockout mutant lines Atclb1-1 and Atclb1-2 after 1 week of incubation on MS medium are shown. The mutant lines Atclb1-1 and Atclb1-2 exhibit higher germination rate (100%) compared with wild-type plants (69.2%±4%). Further, the mutant lines produced slightly longer roots.

The loss of the Atclb gene function in mutants confers an enhanced drought tolerance (FIGS. 3A-3E), salt tolerance (FIGS. 4A-4C), and a modified gravitropic response (not shown) in T-DNA insertion knockout mutant lines. To test water deficit stress response, 4-week-old wild-type and mutant plants (Atclb1-1 and Atclb1-2) were deprived of water for 3 weeks in a growth chamber under a 16-hour photoperiod at 23/23° C. (day/night). At the end of the treatment period, wild-type plants showed signs of water deficit stress as indicated by wilting and yellowing of their rosette leaves, while no stress symptoms were observed in mutant plants (FIG. 3D). Furthermore, plants from both mutant lines (Atclb1-1 and Atclb1-2) were able to maintain their leaf Relative Water Content (RWC) even at 3 weeks of withholding water compared with wild-type plants which showed a rapid decrease in leaf RWC from as early as 1 week after withholding water (FIG. 3C). Hence the observed phenotypic differences between wild-type and mutant plants in relation to water deficit stress tolerance may be attributed to the differences in expression of the Atclb gene (FIG. 3E).

EXAMPLE 2

Tolerance to Salt of Arabidopsis thaliana with Mutated Atclb Gene

Referring to FIGS. 4A-4C, tolerance of mutant lines Atclb1-1 and Atclb1-2 to salt are evaluated. 1-week-old seedlings of wild type, 35S-Atclb overexpression line, Atclb1-1, and Atclb1-2 mutant lines were grown on media containing different concentrations of NaCl. The Atclb knockout lines exhibited increased tolerance to salt stress, while 35S-Atclb overexpression lines were hypersensitive to NaCl. Referring to FIG. 4A, seeds of the Atclb1-1 knockout line were able to germinate on 150 mM NaCl-containing medium. Further, referring to FIG. 4B, sterilized seeds of wild type and knockout lines were germinated on regular MS medium, then 6-day-old seedlings were transferred to Petri plates containing 150 mM NaCl. The seedlings of loss-of-function Atclb1-1 mutant line were able to survive in the presence of 150 mM NaCl for 2 months.

Referring to FIG. 4C, in a separate experiment, one-week-old Arabidopsis thaliana seedlings with 10 to 20 mm long roots on vertical agar plates were transferred to plates supplemented with NaCl and allowed to grow vertically at 23° C. with a 16-hour light period. After 1 week of stress, incremental root growth of each seedling was recorded. Although the incremental root growth of all plants decreased with the increasing salt concentration in the media, both mutant lines exhibited higher root growth compared with wild-type and 35S-Atclb overexpression lines. The incremental root growth of 35S-Atclb plants was less than that of wild-type seedlings and reduced to almost zero at 200 mM NaCl concentration.

According to Examples 1 and 2, it is demonstrated that loss of function of the Atclb gene can lead to increased tolerance to abiotic stress (salt and drought) in Arabidopsis thaliana plant.

EXAMPLE 3

Constructing a Transgenic Rice Plant Tolerant to Abiotic Stress by Silencing OsHP Gene

Atclb gene is playing role of negative regulator of abiotic stress response. In certain embodiments, the silencing of active homologues of Atclb gene will lead to increase of tolerance to abiotic stress. The plant or crop of choice includes, but not limited to, Solanum lycopersicum, Ricinus communis, Populus trichocarpa, Vitis vinifera, Oryza sativa, and Sorghum bicolor.

FIG. 5 illustrates a method for producing a rice plant tolerant to stress conditions by silencing a gene that contains C2 domain that is homologue to C2 domain of Atclb gene, according to one embodiment of the present invention. Vectors for post transcriptional gene silencing (RNA interference (RNAi)) or virus-induced gene silencing (VIGS) can be used for silencing of AtCLB crop homologues.

In the embodiment, Rice cultivar Nipponbare or other rice cultivar is used as the starting material for constructing a transgenic rice plant.

In step 501, through bioinformatics analysis, a first gene, rice OsHP gene, is identified as homologous to Atclb gene of Arabidopsis thaliana based on homology of C2 domains.

In step 503, a recombinant construct is established. In one embodiment, a fragment of C2 domain (300 base pair) of OsHP gene was cloned into special silencing pANDA vector (RNAi vector) under control strong promoter (uniquitin-1 (ubi)) to form the recombinant construct.

In step 505, rice plant cells or rice plants are transformed with the established recombinant construct to form transformed rice cells, and produce a transgenic rice plant from the transformed cells.

In step 507, the silencing of the first gene in the transgenic rice plant is confirmed by analysis of expression of OsHP gene.

In one embodiment, a seed is produced from the transgenic plant.

In certain embodiments, the recombinant construct is capable of silencing the rice OsHP gene, and the transgenic rice plant shows increased abiotic stress tolerance comparing to wild type rice plant.

EXAMPLE 4

Constructing a Transgenic Tomato Plant Tolerant to Abiotic Stress by Silencing SlCLB1 Gene

In one embodiment, the plant of choice is tomato plant Solanum lycopersicum.

FIG. 6 illustrates a method for producing a tomato plant tolerant to abiotic stress conditions by silencing a gene homologue that is homologous to Arabidopsis thaliana Atclb gene, according to one embodiment of the present invention.

In step 601, through bioinformatics analysis, a first gene, rice SlCLB1 gene, is identified as homologous to Atclb gene of Arabidopsis thaliana based on homology of C2 domains.

In step 603, a recombinant construct is established. In one embodiment, a fragment of SlCLB1 gene, corresponding to a polynucleotide of Atclb gene encoding at least part of C2 domain, is cloned into any suitable silencing vector to form the recombinant construct.

In step 605, tomato plant cells are transformed with the established recombinant construct to form transformed tomato cells, and produce a transgenic tomato plant from the transformed cells.

In step 607, the silencing of the first gene in the transgenic tomato plant is confirmed.

In one embodiment, a seed is produced from the transgenic tomato plant.

In certain embodiments, the recombinant construct is capable of silencing the tomato SlCLB1 gene, and the transgenic tomato plant shows increased stress tolerance comparing to wild type tomato plant.

The foregoing description of the exemplary embodiments of the invention has been presented only for the purposes of illustration and description and is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Many modifications and variations are possible in light of the above teaching.

While there has been shown several and alternate embodiments of the present invention, it is to be understood that certain changes can be made as would be known to one skilled in the art without departing from the underlying scope of the invention as is discussed and set forth above and below including claims and drawings. Furthermore, the embodiments described above and claims set forth below are only intended to illustrate the principles of the present invention and are not intended to limit the scope of the invention to the disclosed elements. Moreover, aspects of the present invention are further disclosed and described in Appendix A, which are incorporated herein by references in their entireties as an integral part of the application.

Claims

1. A transgenic plant, comprising: a first gene having a first polynucleotide, wherein the first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1; anda recombinant construct having a second polynucleotide, wherein the second polynucleotide has at least 90% identity to the first polynucleotide or a sequence complimentary to the first polynucleotide, and wherein the recombinant construct is configured to silence the first gene such that the transgenic plant is tolerant to abiotic stress.

2. The transgenic plant of claim 1, wherein the first polynucleotide has at least 50% similarity to the Atclb gene fragment.

3. The transgenic plant of claim 1, wherein the first polynucleotide encodes a C2-like domain, and the C-2 like domain has at least 50% amino acid identity to amino acids 265-345 of SEQ ID NO: 2.

4. The transgenic plant of claim 1, wherein the second polynucleotide is substantially identical to the first polynucleotide or the sequence complimentary to the first polynucleotide.

5. The transgenic plant of claim 1, wherein the recombinant construct is configured to silence the first gene of the transgenic plant by RNA interference, anti-sense construction or virus induced gene silencing (VIGS).

6. The transgenic plant of claim 1, wherein the abiotic stress is water deficit, salt stress, cold stress or a combination thereof.

7. The transgenic plant of claim 1, being formed from a plant comprising Solanum lycopersicum, Ricinus communis, Populus trichocarpa, Vitis vinifera, Oryza sativa, Sorghum bicolor, or the like.

8. The transgenic plant of claim 7 being formed from the Oryza sativa, wherein the first gene is OsHP gene encoding Oryza sativa histidine-containing phosphotransfer protein.

9. The transgenic plant of claim 7 being formed from the Solanum lycopersicum, wherein the first gene is SlCLB1 gene encoding a protein with a Ca2+-dependent lipid-binding domain.

10. A seed of the transgenic plant of claim 1.

11. A transgenic plant, comprising: a mutated first gene such that the transgenic plant is tolerant to abiotic stress, wherein the first gene comprises a first polynucleotide homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1.

12. A method of producing transformed plant cells, comprising: identifying a first gene of plant cells, wherein the first gene has a first polynucleotide, and the first polynucleotide is homologous to a Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1;constructing a recombinant construct for silencing the first gene in the plant cells, wherein the recombinant construct comprises a second polynucleotide, and the second polynucleotide has at least 90% similarity to the first polynucleotide or a sequence complimentary to the first polynucleotide; andtransforming the plant cells with the recombinant construct to form the transformed plant cells,wherein the first gene in the transformed plant cell are silenced by the recombinant construct such that the plant cells are tolerant to an abiotic stress.

13. The method of claim 12, further comprising: confirming the silencing of the first gene in the transformed plant cells.

14. The method of claim 12, further comprising: producing a plant from the transformed plant cells.

15. The method of claim 12, wherein the first polynucleotide has at least 50% similarity to the Atclb gene fragment.

16. The method of claim 12, wherein the first polynucleotide encodes a C2-like domain, and the C-2 like domain has at least 50% amino acid identity to amino acids 265-345 of SEQ ID NO: 2.

17. The method of claim 12, wherein the second polynucleotide is substantially identical to the first polynucleotide or the sequence complimentary to the first polynucleotide.

18. The method of claim 12, wherein the plant cells comprises Solanum lycopersicum cells, Ricinus communis cells, Populus trichocarpa cells, Vitis vinifera cells, Oryza sativa cells, Sorghum bicolor cells, or the like.

19. The method of claim 12, wherein the plant cells are the Oryza sativa cells, and the first gene is OsHP gene encoding Oryza sativa histidine-containing phosphotransfer protein.

20. The method of claim 12, wherein the plant cells are the Solanum lycopersicum cells, and the first gene is SlCLB1 gene encoding a protein with a Ca2+-dependent lipid-binding domain.

21. The method of claim 12, wherein the recombinant construct is configured to silence the first gene of the plant cells by RNA interference, anti-sense construction or virus induced gene silencing (VIGS).

22. The method of claim 12, wherein the abiotic stress is water deficit, salt stress, cold stress or a combination thereof.

23. The method of claim 12, wherein the plant cells are transformed by agrobacterial transformation or bombardment transformation to form the transformed plant cells.

24. Transformed plant cells produced by the method of claim 12.

25. A transgenic plant produced from the transformed plant cells of claim 24.

26. A seed produced by the transgenic plant of claim 25.

27. A method of producing transformed plant cells, comprising: mutating a first gene of plant cells to form the transformed plant cells such that the transformed plant cells are tolerant to an abiotic stress, wherein a first polynucleotide of the first gene is homologous to Atclb gene fragment represented by nucleotide acids 963-1205 of SEQ ID NO:1.