Patent Application
20240352477
The application contains a Sequence Listing which has been submitted electronically in .XML format and is hereby incorporated by reference in its entirety. Said .XML copy, created on Apr. 23, 2024, is named “20240423-ACA0163US-sequence listing.xml” and is 73,728 bytes in size. The sequence listing contained in this .XML file is part of the specification and is hereby incorporated by reference herein in its entirety.
The present invention relates to a method for promoting growth of plants. Particularly, the method of the present invention features overexpression of a calcineurin B-like (CBL) interacting protein kinase15 (CIPK15) having an isoleucine (Ile) residue at position 48 (e.g. a CIPK15 from rice) in plants which can promote growth of the plants. The present invention also relates to a recombinant construct comprising a nucleic acid encoding the CIPK15 operably linked to a promoter. The present invention further relates to a transgenic plant overexpressing the CIPK15 exhibiting improved growth compared to a non-transgenic plant counterpart.
Flooding is a widespread natural disaster that can account for up to 20% of yield losses of global food production1. Due to the slow diffusion of oxygen (O2) in water, plant roots submerged under water suffer O2 deficiency that impairs respiration and nutrient uptake from the soil, leading to cell damage, growth retardation and even death. Rice is the only cereal capable of growth under aquatic environments due to its activation of various anatomical, metabolic and/or morphological mechanisms to adapt to periods of hypoxia or anoxia. Such mechanisms include early production of enzymes for starch conversion to sugars for anaerobic germination and seedling development2, glycolysis in the absence of O2 through fermentative metabolism3, specific structures (e.g., aerenchyma in parenchymal tissues) that improve access to O24, gibberellin- and ethylene-promoted internode elongation to allow plants to extend above the water surface for gas exchange (e.g., deep water rice)3, and energy conservation during flooding and drought tolerance after recovery from flooding (e.g., lowland rice)5.
Rice is one of the most important crops in the world and is the principal food of nearly 50% of the world's population. Direct seeding, an important agricultural practice for rice, is increasingly employed by farmers in rain-fed and irrigated fields in Asia given its advantages of reduced labor, energy and water use, and production costs6. Underwater germination and seedling development is a prerequisite for effective direct-seeded rice cultivation. Despite tolerance of rice roots to waterlogging and partial submergence at vegetative stages, most rice varieties are extremely sensitive to hypoxia during germination and early seedling growth stages6. Under hypoxia, tolerant rice genotypes exhibit speedy hydrolysis of starch to sugars to fuel anaerobic metabolism, germination and coleoptile elongation, root and leaf development, and seedling emergence above the water surface2,7,8. Early increases in α-amylase (αAmy) activity (a few hours after seed imbibition) and late increases in ethylene accumulation (3 days after seed sowing) are tightly associated with enhanced seedling elongation and survival of submergence-tolerant rice varieties9.
Among the major cereals, only rice seeds produce the αAmy needed to mobilize starch into fermentable sugars for NAD+ recycling and ATP generation during anaerobic germination and coleoptile development10. The sugar starvation-inducible transcription factor MYBS1 binds to and activates the αAmy promoter, with energy-sensing SNF-related protein kinase 1A (SnRK1A) upregulating MYBS1 in response to sugar starvation and hypoxia2,11-13. CIPK15, a calcineurin B-like (CBL) protein-interacting Ser/Thr protein kinase induced by sugar starvation and hypoxia, activates the SnRK1A-dependent pathway to induce αAmy and alcohol dehydrogenase genes ADH1/2, and to control sugar and energy production during anaerobic germination and seedling growth2,7. CIPK15 knock-out mutation in rice impairs both underwater germination and seedling growth, as well as mature plant growth in waterlogged soil2.
The coleoptile is a conical plant structure and, upon exposure to O2, it undergoes splitting, senescence, and aerenchyma development to facilitate leaf and root growth14. Lysigenous aerenchyma is formed by the development of longitudinal gaseous channels resulting from death and lysis of cortical cells in roots and of parenchyma cells in shoots15. In rice, aerenchyma is also developed in the leaf midrib, sheath and stem internodes16, providing an internal channel for O2 transmission from shoots to root tips, which contributes to plant tolerance to waterlogged soil15. Although rice coleoptile elongation is rapid under water, root elongation is rather slow17. Active root growth occurs as coleoptiles approach the water surface where the O2 concentration is higher8,9, indicating that O2 acquisition by the coleoptile facilitates root development.
In rice roots, aerenchyma is constitutively formed in well-drained soils and further induced upon soil waterlogging, with induction being mediated by an ethylene-reactive oxygen species (ROS)-dependent programed cell death (PCD) pathway15,18. Rice produces more ethylene in its roots than maize due to higher expression under hypoxia of genes in the ethylene biosynthesis pathway, such as ACC SYNTHASE 1 (ACS1) and ACC OXIDASE 5(ACO5)19. Excess ethylene accumulation in root cortical cells promotes expression of RESPIRATORY BURST OXIDASE HOMOLOG H (RBOHH), the protein product of which converts O2 to O2−, thereby increasing H2O2 levels15. The resulting ROS signal further induces cell wall-degrading enzymes to trigger PCD in cortical cells to form aerenchyma20,21 Despite our comprehensive understanding of how aerenchyma development is regulated by ethylene under hypoxia, the mechanism connecting hypoxia-sensing to ethylene biosynthesis and signaling has remained unclear.
Hexokinases (HXKs) are dual-function proteins that not only catalyze the ATP-dependent phosphorylation of hexose in the first step of glycolysis, but also serve as a sugar sensor monitoring sugar level in cells22,23. Most higher organisms express multiple HXK isoforms that are associated with various cellular membranes to exert diverse biological functions24. Arabidopsis has six HXK members and rice has ten25,26, but very few have been functionally characterized. In Arabidopsis, HXK1 senses glucose and integrates nutrient, light and hormone signaling networks to control growth and development23. HXKs mediate sugar feed-back repression of genes essential for photosynthesis and starch degradation, but the underlying mechanism remains largely unknown27. The voltage-dependent anion channel (VDAC) is the most abundant protein in the mitochondrial outer membrane and it is the major channel responsible for transporting ions, Ca2+, ADP/ATP and other metabolites in and out of these organelles28. In animal cells, interaction of VDAC1 with HXKs on mitochondrial membranes plays important roles in regulating cellular energy production, metabolism and apoptosis29.
The development of an aerated root system in waterlogged soil is a fundamental requirement for the flooding tolerance displayed by plants. Understanding the mechanism by which rice root growth is promoted under flooding or hypoxia is not only of fundamental scientific significance, but it is also important for breeding rice and other crops with enhanced flooding tolerance. There is also a need to provide an approach to promote growth, yield and root development of plants and enhance their tolerance to environmental stress.
In this invention, it is unexpectedly found that overexpression of a calcineurin B-like (CBL) interacting protein kinase15 (CIPK15) in a plant can improve growth, yield and/or root development of the plant, wherein the CIPK15 has an isoleucine (Ile) residue at a position corresponding to position 48 of SEQ ID NO: 1 (e.g. a CIPK15 from rice). The transgenic plant also exhibits enhanced tolerance to environmental stress e.g. drought, salinity and flooding stresses, and/or increased ethylene production.
Therefore, in one aspect, the present invention provides a method for promoting growth, yield and/or root development of a plant, comprising
In some embodiments, the CIPK15 is a CIPK15 from rice.
In some embodiments, the CIPK15 is a CIPK15 from barley, wheat, rye, oat, millet, corn, bamboo, sugarcane, onion, leek, ginger, stiff brome, millet, green foxtail, sorghum, Kans grass or Hall's panicgrass, having an isoleucine (Ile) substituent at a position corresponding to position 48 of SEQ ID NO: 1.
In some embodiments, the CIPK15 comprises
In some embodiments, the promoter is a root-specific promoter.
In some embodiments, the promoter is a native rice CIPK15 promoter.
In some embodiments, the transgenic plant exhibits improved growth, yield and/or root development as compared with a non-transgenic plant counterpart under aerobic or hypoxic conditions.
In some embodiments, the transgenic plant exhibits increased plant height, elongated coleoptiles and shoot, higher grain yield, longer roots, larger root radius, and/or more aerenchyma.
In some embodiments, the transgenic plant further exhibits enhanced tolerance to environmental stress.
In some embodiments, the environmental stress includes drought, salinity and/or flooding stresses.
In some embodiments, the transgenic plant further exhibits enhanced ethylene production.
In some embodiments, the transgenic plant is a monocot plant.
In some embodiments, the transgenic plant is rice, barley, wheat, rye, oat, corn, bamboo, sugarcane, onion, leek, ginger, stiff brome, millet, green foxtail, sorghum, cutgrasses, Kans grass or Hall's panicgrass.
In some embodiments, the transgenic plant is a dicot plant.
In some embodiments, the transgenic plant is Arabidopsis, soybean, peanut, sunflower, safflower, cotton, tobacco, tomato, pea, chickpea, pigeon pea or potato.
In another aspect, the present invention provides a recombinant construct comprising a nucleic acid encoding CIPK15 operably linked to a promoter, wherein the CIPK15 has an isoleucine (Ile) residue at a position corresponding to position 48 of SEQ ID NO: 1.
In some embodiments, the CIPK15 is a CIPK15 from rice.
In some embodiments, the CIPK15 is a CIPK15 from barley, wheat, rye, oat, millet, corn, bamboo, sugarcane, onion, leek, ginger, stiff brome, millet, green foxtail, sorghum, Kans grass or Hall's panicgrass, having an isoleucine (Ile) substituent at a position corresponding to position 48 of SEQ ID NO: 1.
In some embodiments, the CIPK15 comprises
In some embodiments, the promoter is a root-specific promoter.
In some embodiments, the promoter is a native rice CIPK15 promoter.
In a further aspect, the present invention provides a transgenic plant comprising an exeogenous nucleic acid operably linked to a promoter, wherein the exogenous nucleic acid (a transgene) encodes CIPK15. In some embodiments, the transgenic plant is generated by transformation with a recombinant construct encoding CIPK15 as described herein.
In some embodiments, the transgenic plant exhibits improved growth, yield and/or root development as compared with a non-transgenic plant counterpart.
In some embodiments, the transgenic plant exhibits improved growth, yield and/or root development as compared with a non-transgenic plant counterpart under aerobic or hypoxic conditions.
In some embodiments, the transgenic plant exhibits increased plant height, elongated coleoptiles and shoot, higher grain yield, longer roots, larger root radius, and/or more aerenchyma.
In some embodiments, the transgenic plant further exhibits enhanced tolerance to environmental stress.
In some embodiments, the environmental stress includes drought, salinity and/or flooding stresses.
In some embodiments, the transgenic plant further exhibits enhanced ethylene production.
In some embodiments, the transgenic plant is a monocot plant.
In some embodiments, the transgenic plant is rice, barley, wheat, rye, oat, corn, bamboo, sugarcane, onion, leek, ginger, stiff brome, millet, green foxtail, sorghum, cutgrasses, Kans grass or Hall's panicgrass.
In some embodiments, the transgenic plant is a dicot plant.
In some embodiments, the transgenic plant is Arabidopsis, soybean, peanut, sunflower, safflower, cotton, tobacco, tomato, pea, chickpea, pigeon pea or potato.
Also provided is a gene-edited plant having a genome comprising a nucleic acid encoding a CIPK15 having an isoleucine (Ile) substituent at a position corresponding to position 48 of SEQ ID NO: 1.
In particular, the plant, before genome edition, originally has a natural gene encoding a CIPK15 having an amino acid residue other than isoleucine (Ile) at a position corresponding to position 48 of SEQ ID NO: 1 in its genome, and after genome edition, the gene is modified to encode a mutant CIPK15 having an isoleucine (Ile) substituent at the position corresponding to position 48 of SEQ ID NO: 1 in its genome. In some examples, the amino acid residue other than isoleucine (Ile) at a position corresponding to position 48 of SEQ ID NO: 1 is valine (Val) or alanine (Ala).
In some embodiments, the mutant CIPK15 comprises (a) an amino acid sequence selected from the group consisting of SEQ ID NOs:19-32 or (b) an amino acid sequence having a sequence identity of at least 80% with the amino acid sequence of (a) and having an isoleucine (Ile) residue at position 48 of SEQ ID NO: 1.
The details of one or more embodiments of the invention are set forth in the description below. Other features or advantages of the present invention will be apparent from the following detailed description of several embodiments, and also from the appending claims.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawings will be provided by the Office upon request and payment of the necessary fee.
The foregoing summary, as well as the following detailed description of the invention, will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the invention, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the invention is not limited to the precise arrangements and instrumentalities shown.
In the drawings:
Unless defined otherwise, all technical and scientific terms used herein have the same meanings as is commonly understood by one of skill in the art to which this invention belongs.
As used herein, the articles “a” and “an” refer to one or more than one (i.e., at least one) of the grammatical object of the article. By way of example, “an element” means one element or more than one element.
As used herein, the term “comprise” or “comprising” is generally used in the sense of include/including which means permitting the presence of one or more features, ingredients or components. The term “comprise” or “comprising” encompasses the term “consists” or “consisting of.”
As used herein, the term “about” or “approximately” refers to a degree of acceptable deviation that will be understood by persons of ordinary skill in the art, which may vary to some extent depending on the context in which it is used. In general, “about” or “approximately” may mean a numeric value having a range of ±10% around the cited value
As used herein, the term “polypeptide” or proteins refers to a polymer composed of amino acid residues linked via peptide bonds.
As used herein, the term “corresponding to” refers to a residue at the enumerated position in a protein or peptide, or a residue that is analogous, homologous, or equivalent in position to the enumerated residue in a different protein or peptide. Determining corresponding amino acid residues can be done by aligning the sequences and identifying residues that like across from one another in the resultant alignment. Namely, the residue number or position of a given amino acid sequence is designated with respect to the reference sequence rather than by the actual numerical position of that residue within the given amino acid sequence. The same corresponding rule is applicable to nucleotides in polynucleotide sequences.
As used herein, the term “substantially identical” refers to two sequences having 80% or more, preferably 85% or more, more preferably 90% or more, even more preferably 95% or more homology.
As used herein, the term “polynucleotide” or “nucleic acid” refers to a polymer composed of nucleotide units. Polynucleotides include naturally occurring nucleic acids, such as deoxyribonucleic acid (“DNA”) and ribonucleic acid (“RNA”) as well as nucleic acid analogs including those which have non-naturally occurring nucleotides. Polynucleotides can be synthesized, for example, using an automated DNA synthesizer. The term “nucleic acid” typically refers to large polynucleotides. It will be understood that when a nucleotide sequence is represented by a DNA sequence (i.e., A, T, G, C), this also includes an RNA sequence (i.e., A, U, G, C) in which “U” replaces “T.” The term “cDNA” refers to a DNA that is complementary or identical to an mRNA, in either single stranded or double stranded form.
As used herein, the term “complementary” refers to the topological compatibility or matching together of interacting surfaces of two polynucleotides. Thus, the two molecules can be described as complementary, and furthermore the contact surface characteristics are complementary to each other. A first polynucleotide is complementary to a second polynucleotide if the nucleotide sequence of the first polynucleotide is identical to the nucleotide sequence of the polynucleotide binding partner of the second polynucleotide. Thus, the polynucleotide whose sequence 5′-TATAC-3′ is complementary to a polynucleotide whose sequence is 5′-GTATA-3′.”
As used herein, the term “encoding” refers to the inherent property of specific sequences of nucleotides in a polynucleotide (e.g., a gene, a cDNA, or an mRNA) to serve as templates for synthesis of other polymers and macromolecules in biological processes having either a defined sequence of nucleotides (i.e., rRNA, tRNA and mRNA) or a defined sequence of amino acids and the biological properties resulting therefrom. Therefore, a gene encodes a protein if transcription and translation of mRNA produced by that gene produces the protein in a cell or other biological system. It is understood by a skilled person that numerous different polynucleotides and nucleic acids can encode the same polypeptide as a result of the degeneracy of the genetic code. It is also understood that skilled persons may, using routine techniques, make nucleotide substitutions that do not affect the polypeptide sequence encoded by the polynucleotides described there to reflect the codon usage of any particular host organism in which the polypeptides are to be expressed. Therefore, unless otherwise specified, a “nucleotide sequence encoding an amino acid sequence” includes all nucleotide sequences that are degenerate versions of each other and that encode the same amino acid sequence. Nucleotide sequences that encode proteins and RNA may include introns.
As used herein, the term “overexpression” can refer to the production of a gene product in transgenic plants that exceeds levels of production in non-transgenic plants, including but not limited to constitutive or induced expression.
As used herein, the term “transgenic plant” or “transgenic line” refers to a plant that contains a recombinant nucleotide sequence that encodes a gene i.e. a transgene. The transgenic plant can be grown from a recombinant cell.
As used herein, the term “genome editing” or “gene-editing” can refer to introducing a targeted variation and/or mutation into the nucleotide sequence of plant cells, including knocking-out or knocking-in a specific gene, or introducing a variation into a coding DNA sequence or a non-coding DNA sequence that produces no protein. For the purpose of the present disclosure, the genome editing may mean introducing a mutation or change (e.g. an isoleucine (Ile) substituent at a position corresponding to position 48 of SEQ ID NO: 1) using a Cas protein and a guide RNA, for example.
CIPK15 is known as a plant-specific Ser-Thr protein kinase containing a conserved NAF (Asn-Ala-Phe) domain, which is critical for the interaction with calcineurin B-like proteins. CIPK15 can be found in a variety of plants. CIPK15 comprises a total of 400 to 450 amino acid residues in length. CIPK15 comprises from N-terminal to C-terminal a catalytic kinase domain, a junction domain and a regulatory domain, wherein the catalytic kinase domain includes an activation loop at a region from position 153 to 182 with a threonine (T) at position 171, and the regulatory domain includes a NAF (Asn-Ala-Phe) domain at a region from position 298 to 333, with respect to SEQ ID NO: 1. See
Specifically, a native CIPK15 from rice may have the amino acid sequence of SEQ ID NO: 1 (OsCIPK15, Oryza sativa), SEQ ID NO: 2 (ObCIPK15, Oryza barthii), SEQ ID NO: 3 (OgCIPK15, Oryza glaberrima) or SEQ ID NO: 4 (OrCIPK15, Oryza rufipogon), wherein the amino acid residue at position 48 is isoleucine (Ile 48). A native CIPK15 from stiff brome may have the amino acid sequence of SEQ ID NO: 5 (BdCIPK15, Brachypodium distachyon), a native CIPK15 from millet may have the amino acid sequence of SEQ ID NO: 6 (SiCIPK15, Setaria Italica), a native CIPK15 from green foxtail may have the amino acid sequence of SEQ ID NO: 7 (SvCIPK15, Setaria viridis), a native CIPK15 from sorghum may have the amino acid sequence of SEQ ID NO: 8 (SbCIPK15, Sorghum bicolor), and a native CIPK15 from barley may have the amino acid sequence of SEQ ID NO: 9 (HvCIPK15, Hordeum vulgare), wherein the amino acid residue at position 48 is valine (Val 48). A native CIPK15 from wheat may have the amino acid sequence of SEQ ID NO: 10 (TaCIPK15, Triticum aestivum), SEQ ID NO: 11 (TridCIPK15, Triticum dicoccoides), or SEQ ID NO: 12 (Tritd, Triticum turgidum), wherein the amino acid residue at position 53 is valine (Val 53) which is also called Val 48 since the position Val 53 corresponds to position 48 with respect to SEQ ID NO: 1 because of four amino acid residues at N-terminal of SEQ ID NO: 10-12. A native CIPK15 from wheat may have the amino acid sequence of SEQ ID NO: 13 (TuGCIPk15, Triticum Urartu), wherein the amino acid residue at position 48 is valine (Val 48). A native CIPK15 from corn may have the amino acid sequence of SEQ ID NO: 14 (ZmCIPK15, Zea mays), a native CIPK15 from cutgrasses may have the amino acid sequence of SEQ ID NO: 15 LpCIPK15 (Leersia perrieri), a native CIPK15 from Kans grass may have the amino acid sequence of SEQ ID NO: 16 (SsCIPK15, Saccharum spontaneum), a native CIPK15 from Hall's panicgrass may have the amino acid sequence of SEQ ID NO: 17 (PhCIPK15, Panicum hallii), and a native CIPK15 from rye may have the amino acid sequence of SEQ ID NO: 18 (ScCIPK15, Secale cereal), wherein the amino acid residue at position 48 is valine (Val 48).
Oryza sativa
Oryza barthii
Oryza glaberrima
Oryza rufipogon
Brachypodium
distachyon
Setaria Italica
Setaria viridis
Sorghum bicolor
Hordeum vulgare
Triticum aestivum
Triticum dicoccoides
Triticum turgidum
Triticum Urartu
Zea mays
Leersia perrieri
Saccharum spontaneum
Panicum hallii
Secale cereal
As used herein, the term “CIPK15,” unless indicated otherwise, refers to “CIPK15 with Ile 48” namely a CIPK15 from a plant species having isoleucine at a position corresponding to position 48 of SEQ ID NO: 1.
In some embodiments, CIPK15 as described herein can be a native CIPK15 from rice where the amino acid residue at position 48 is isoleucine (Ile 48) in nature. Examples of CIPK15 from rice may have the amino acid sequence of SEQ ID NO: 1, 2, 3 or 4.
In some embodiments, CIPK15 as described herein can be a CIPK15 from other plant species with modification where the amino acid residue at a position corresponding to position 48 with respect to SEQ ID NO: 1 is changed to isoleucine (Ile). Examples of modified CIPK15 may have the amino acid sequence ofany of SEQ ID NO: 19-32 which are identical to SEQ ID NO: 5-18, respectively, except that the amino acid residue at a position corresponding to position 48 with respect to SEQ ID NO: 1 is changed to isoleucine (Ile). CIPK15 as described herein can also include those comprising an amino acid sequence which has Ile 48 and are substantially identical to the amino acid sequences constituting CIPK15 as described herein. Specifically, CIPK15 as described herein may include an amino acid sequence with Ile 48, having at least 80% (e.g. 82%, 84%, 85%, 86%, 88%, 90%, 92%, 94%, 95%, 96%, 98%, or 99%) identity to SEQ ID NO: 1-4 and 19-32.
Brachypodium distachyon
Setaria Italica
Setaria viridis
Sorghum bicolor
Hordeum vulgare
Triticum aestivum
Triticum dicoccoides
Triticum turgidum
Triticum Urartu
Zea mays
Leersia perrieri
Saccharum spontaneum
Panicum hallii
Secale cereal
1 Valine (V) or Alanine (A) at position 48 is substituted with isoleucine (I)
2 Valine (V) at position 53 is substituted with isoleucine (I)
It is understandable a polypeptide may have a limited number of changes or modifications that may be made within a certain portion of the polypeptide irrelevant to its activity or function and still result in a molecule with an acceptable level of equivalent biological activity or function. Modifications and changes may be made in the structure of such polypeptides and still obtain a molecule having similar or desirable characteristics. For example, certain amino acids may be substituted for other amino acids in the peptide/polypeptide structure (other than the conserved region) without appreciable loss of activity. Amino acid substitutions are generally based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. For example, arginine (Arg), lysine (Lys), and histidine (His) are all positively charged residues; and alanine (Ala), glycine (Gly) and serine (Ser) are all in a similar size. Therefore, based upon these considerations, arginine (Arg), lysine (Lys) and histidine (His); and alanine (Ala), glycine (Gly) and serine (Ser) may be defined as biologically functional equivalents. One can readily design and prepare recombinant genes for microbial expression of polypeptides having equivalent amino acid residues.
To determine the percent identity of two amino acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in the sequence of a first amino acid sequence for optimal alignment with a second amino acid sequence). In calculating percent identity, typically exact matches are counted. The determination of percent homology or identity between two sequences can be accomplished using a mathematical algorithm known in the art, such as BLAST and Gapped BLAST programs, the NBLAST and XBLAST programs, or the ALIGN program.
The present invention provides a recombinant construct encoding CIPK15. In particular, the recombinant construct comprises a nucleotide sequence encoding CIPK15 operably linked to a promoter.
As used herein, the term “recombinant construct” refers to a polynucleotide or nucleic acid having sequences that are not naturally joined together. A recombinant construct may be present in the form of a vector. “Vectors” may contain a given nucleotide sequence of interest and a regulatory sequence. Vectors may be used for expressing the given nucleotide sequence (expression vector) or maintaining the given nucleotide sequence for replicating it, manipulating it or transferring it between different locations (e.g., between different organisms). Vectors can be introduced into a suitable host cell for the above-mentioned purposes. A “recombinant cell” refers to a cell where a recombinant nucleic acid is introduced.
As used herein, the term “operably linked” may mean that a polynucleotide is linked to an expression control sequence in such a manner to enable expression of the polynucleotide when a proper molecule (such as a transcriptional factor) is bound to the expression control sequence.
As used herein, the term “expression control sequence” or “regulatory sequence” means a DNA sequence that regulates the expression of the operably linked nucleic acid sequence in a certain host cell.
Examples of vectors include, but are not limited to, plasmids, cosmids, phages, YACs or PACs. Typically, in vectors, the given nucleotide sequence is operatively linked to the regulatory sequence such that when the vectors are introduced into a host cell, the given nucleotide sequence can be expressed in the host cell under the control of the regulatory sequence. The regulatory sequence may comprise, for example and without limitation, a promoter sequence (e.g., the cytomegalovirus (CMV) promoter, simian virus 40 (SV40) early promoter, T7 promoter, and alcohol oxidase gene (AOX1) promoter), a start codon, a replication origin, enhancers, an operator sequence, a secretion signal sequence (e.g., □-mating factor signal) and other control sequence (e.g., Shine-Dalgano sequences and termination sequences). Preferably, vectors may further contain a marker sequence (e.g., an antibiotic resistant marker sequence) for the subsequent screening procedure. In vectors, the given nucleotide sequence of interest may be connected to another nucleotide sequence other than the above-mentioned regulatory sequence such that a fused polypeptide is produced and beneficial to the subsequent purification procedure. Said fused polypeptide includes, but is not limited to, a His-tag fused polypeptide and a GST fused polypeptide. The given nucleotide sequence of interest may also be connected to a reporter gene e.g. β-glucuronidase (GUS) or green fluorescent protein (GFP) to monitor promoter activity and gene expression.
Where the expression vector is constructed for a plant cell, several suitable promoters known in the art may be used, including but not limited to the Figwort mosaic virus 35S promoter, the cauliflower mosaic virus (CaMV) 35S promoter, the commelina yellow mottle virus promoter, the rice cytosolic triosephosphate isomerase (TPI) promoter, the rice actin 1 (Act1) gene promoter, the uniquitin (Ubi) promoter, the rice amylase gene promoter, the adenine phosphoribosyltransferase (APRT) promoter of Arabidopsis, the mannopine synthase and octopine synthase promoters.
In some embodiments, a promoter described herein may be heterologous to the nucleic acid encoding a target gene in the vector. As used herein, a promoter heterologous to a coding sequence (a gene) refers to a promoter that is not the natural promoter that controls (drives) expression of the gene in native state. For example, the vector of the present disclosure may comprise a promoter derived from a non-CIPK15 gene.
In some examples, the promoter described herein can be constitutive, which initiates transcription independent of the influence of regulation. Exemplary constitutive promoters include, but are not limited to a maize ubiquitin (Ubi) promoter, a rice actin (Act1) promoter, and a cauliflower mosaic virus 35S (CaMV35S) promoter.
In other examples, the promoter described herein can be inducible, which initiates transcription in a regulated manner, for example, in the presence or absence of a particular factor. Exemplary inducible promoters include an ethanol inducible promoter (e.g., a A1cR/A1cA promoter) or a β-estradiol inducible promoter (e.g., a XVE promoter, see Examples section below). Exemplary promoters inducible by biotic or abiotic stress (e.g., osmotic stress, drought stress, salt stress, high or low temperatures, hypoxia, anoxia, hydration, pH, chemicals, hormones or a combination thereof) include an Arabidopsis rd29A promoter, an Arabidopsis corl SA promoter, an Arabidopsis kinl promoter, an Arabidopsis heat-shock factor (HSF) promoter, and an alpha-amylase promoter.
In some embodiments, the promoter described herein may be homologous to the nucleic acid encoding a target gene in the vector. As used herein, a promoter homologous to a coding sequence (a gene) refers to a promoter that is the natural promoter that controls (drives) expression of the gene in native state. For example, the vector of the present disclosure may comprise a promoter derived from a native CIPK15 gene (a native CIPK15 promoter).
In certain example, a promoter sequence as used in the invention is a Ubi promoter having SEQ ID NO: 34.
In certain example, a promoter sequence as used in the invention is a XVE promoter having SEQ ID NO: 35.
In certain example, a promoter sequence as used in the invention is a native rice CIPK15 promoter having SEQ ID NO: 36.
In some embodiments, a vector comprising a nucleic acid encoding CIPK15 operably linked to a Ubi promoter comprises a fused promoter/coding region fragment of SEQ ID NO: 37 (Ubi: CIPK15).
In some embodiments, a vector comprising a nucleic acid encoding CIPK15 operably linked to a XVE promoter comprises a fused promoter/coding region fragment of SEQ ID NO: 38 (XVE: CIPK15).
In some embodiments, a vector comprising a nucleic acid encoding CIPK15 operably linked to a CIPK15 promoter comprises a fused promoter/coding region fragment of SEQ ID NO: 39 (CIPK15: CIPK15).
A recombinant construct described herein may be prepared via conventional recombinant technology.
Some aspects of the present invention provide host cells (e.g., an Agrobacterium cell or a plant cell) comprising any of the vectors as described herein. These host cells (or called recombinant cells) carry exogenous/foreign genetic materials (e.g., the vectors described herein), which can be introduced into the host cell via conventional practice. “Exogenous genetic materials” as used herein can mean that the genetic materials are not originally present in the cells and instead artificially introduced into the cells of a parent thereof. In some instances, the exogenous genetic material may be derived from a different species as the host cell. In some other instances, the exogenous genetic material may be derived from the same species as the host cell and introduced into the host cell such that the resultant recombinant cell comprises extra copies of the genetic material as compared with the wild-type counterpart. The term “transformation” or “transform” as used herein refers to the introduction of exogenous genetic materials into a host cell such as a plant cell.
In certain embodiments, the host cell may be an Agrobacterium host cell. In certain embodiments, the host cell may be a plant cell, for example, a cell from a monocotyledonous plant or a dicotyledonous plant.
Suitable conventional methods are available to make the recombinant cells described herein. Examples of such methods include electroporation, PEG operation, particle bombardment, micro injection of plant cell protoplasts or embryogenic callus or other plant tissue, or Agrobacterium-mediated transformation.
Transgene expression (e.g., before and after transformation of a vector presented herein in a host cell) may be detected using methods known in the art. For example, reverse transcriptional polymerase chain reaction (RT-PCR) may be used to determine mRNA expression. Additional detection methods include western blot analysis and an enzyme-linked immunosorbent assay (ELISA) with a proper antibody for protein detection.
A transgenic plant can be grown from a recombinant cell. Therefore, the present invention provides a transgenic plant comprising an exeogenous nucleic acid operably linked to a promoter, wherein the exeogenous nucleic acid (a transgene) encodes CIPK15.
As used herein, plants may be a full plant or a part thereof, including a fruit, shoot, stem, root, leaf or seed, or various types of cells in culture (e.g., single cells, protoplasts, embryos, callus, protocorm-like bodies, and other types of cells). As described above, a plant of the present disclosure may be a monocot or a dicot.
In some embodiments, the plants as described herein are monocotyledonous plants. Examples of monocots include, but are not limited to, rice, barley, wheat, rye, oat, corn, bamboo, sugarcane, onion, leek, ginger, stiff brome, millet, green foxtail, sorghum, cutgrasses, Kans grass or Hall's panicgrass.
In other embodiments, the plants described herein are dicotyledonous plants. Exemplary dicot plants include Arabidopsis, soybean, peanut, sunflower, safflower, cotton, tobacco, tomato, pea, chickpea, pigeon pea and potato.
A variety of procedures that can be used to engineer a stable transgenic plant are available in this art. In some embodiments, the transgenic plant is produced by transforming a tissue of a plant, such as a protoplast or leaf-disc of the plant, with a recombinant Agrobacterium cell comprising a nucleic acid encoding a desired protein (e.g. CIPK15) and generating a whole plant from the transformed plant tissue. In some embodiments, a nucleic acid encoding a desired protein can be introduced into a plant via gene gun technology, particularly if transformation with a recombinant Agrobacterium cell is not efficient in the plant. To prepare a transgenic plant, it is preferably that the expression vector as used herein carries one or more selection markers for selection of the transformed plants, for example, genes conferring the resistance to antibiotics such as hygromycin, ampicillin, gentamycine, chloramphenicol, streptomycin, kanamycin, neomycin, geneticin and tetracycline, URA3 gene, genes conferring the resistance to any other toxic compound such as certain metal ions or herbicide, such as glufosinate or bialaphos.
Specifically, a transgenic plant according to the present invention comprises a transgene encoding CIPK15 allowing for overexpression of CIPK15 in the transgenic plant. For example, the level of CIPK15 in the transgenic plant may be at least 10% higher (e.g., 20% higher, 30% higher, 50% higher, 1-fold higher, 2-fold higher, 5-folder higher, 10-fold higher, or above) as compared with that in non-transgenic (wild type) counterpart plants. In some instances, the wild-type parent does not express the such CIPK15.
According to the present invention, a transgenic plant as disclosed herein exhibits improved growth, yield and/or root development. For example, a transgenic plant as disclosed herein exhibits increased plant height, elongated coleoptiles and shoot, higher grain yield, longer roots, larger root radius, and/or more aerenchyma, compared to a non-transgenic (wild type) counterpart plant, under the same growing conditions. In some embodiments, the growing condition is aerobic or hypoxic.
In some embodiments, a transgenic plant as disclosed herein further exhibits enhanced tolerance to environmental stress. For example, a transgenic plant as disclosed herein exhibits improved ability to survive under environmental stress. In some instances, the environmental stress includes drought, salinity and/or flooding stresses.
In some embodiments, a transgenic plant as disclosed herein further exhibits enhanced ethylene production.
Accordingly, the present invention also provides a method of producing the transgenic plants described herein. The method may comprise: (a) transforming plant cells with a recombinant construct comprising a nucleic acid operably linked to a promoter to obtain recombinant plant cells overexpressing CIPK15, wherein the nucleic acid encodes CIPK15; and (b) growing the recombinant plant cells obtained in (a) to generate the transgenic plants.
The present invention further provides a method for improving growth, yield and/or root development of a plant by overexpressing CIPK15 in the plant. In particular, the method comprises (a) transforming plant cells with a recombinant construct comprising a nucleic acid operably linked to a promoter to obtain recombinant plant cells overexpressing CIPK15, wherein the nucleic acid encodes CIPK15; (b) growing the recombinant plant cells obtained in (a) to generate a plurality of transgenic plants; and (c) selecting a transgenic plant from the plurality of transgenic plants generated in (b) that exhibits improved growth, yield and/or root development as compared with a non-transgenic plant counterpart growing under the same conditions. In some embodiments, the transgenic plant as selected exhibits improved growth, yield and/or root development as compared with a non-transgenic plant counterpart under aerobic or hypoxic condition. In some examples, the improved growth, yield and/or root development may include increased plant height, elongated coleoptiles and shoot, higher grain yield, longer roots, larger root radius, and/or more aerenchyma. In some embodiments, the transgenic plant as selected further exhibits enhanced tolerance to environmental stress, such as drought, salinity and/or flooding stresses.
Genome/gene editing methods are also available to introduce targeted mutation in plants. Typically, targeted gene editing may include deletion, insertion and/or substitution at one or more given sites in the genome to give mutation to genes in the plant cells. Examples of gene editing methods include zinc finger nuclease (ZFN), transcription activator-like effector DNA binding protein (TALLEN) and clustered regularly interspaced short palindromic repeats (CRISPR)/Cas system. Typically, in CRISPR/Cas system, the key components include a Cas protein (endonuclease) and a guide RNA (gRNA) containing a 20-nt guide sequence that can direct the Cas protein to the target site. The Cas protein can be a Cas9 enzyme that may be one from Streptococcus pyogenes while other Cas9 homologs may also be used. The Cas protein creates a DNA double-strand break (DSB) in the genome.
During the DSB repair, gene mutagenesis or replacement can be obtained via non-homologous end joining leading to nucleotide deletion, insertions and substitution around the DSB region and disrupting gene function, or by homologous recombination to provide precise gene editing in the presence of a repair template. In some embodiments, a binary vector is designed and used which expresses two elements, a Cas9 protein and a gRNAs with a target sequence e.g. CIPK15 (V48I), to cleave target genomic regions. Delivery of a Cas protein and a gRNA may be through direct injection or cell transfection using known methods, for example, Agrobacterium, gene gun, protoplast transfection and viral delivery. In some examples, a Cas protein and a gRNA or a binary vector expressing both are/is introduced into plants through Agrobacterium-mediated transformation procedures and a gene-edited plant is regenerated from the transformed plant cells. In some examples, a Cas protein and a gRNA or a binary vector expressing both are/is introduced into an isolated plant protoplast and a gene-edited plant is regenerated from the transfected plant protoplast.
In some embodiments, a gene-edited plant is thus provided which comprises a genome comprising a nucleic acid encoding a CIPK15 having an isoleucine (Ile) substituent at a position corresponding to position 48 of SEQ ID NO: 1. In particular, the plant, before genome edition, originally has a natural gene encoding a CIPK15 having an amino acid residue other than isoleucine (Ile) at a position corresponding to position 48 of SEQ ID NO: 1 in its genome, and after genome edition, the gene is modified to encode a mutant CIPK15 having an isoleucine (Ile) substituent at the position corresponding to position 48 of SEQ ID NO: 1 in its genome. In some examples, the amino acid residue other than isoleucine (Ile) at a position corresponding to position 48 of SEQ ID NO: 1 includes valine (Val) or alanine (Ala).
In some embodiments, the mutant CIPK15 comprises (a) an amino acid sequence selected from the group consisting of SEQ ID NOs:19-32; or (b) an amino acid sequence having a sequence identity of at least 80% with the amino acid sequence of (a) and having an isoleucine (Ile) residue at position 48 of SEQ ID NO: 1.
The present invention is further illustrated by the following examples, which are provided for the purpose of demonstration rather than limitation. Those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
In this study, we show that protein kinase CIPK15 transmits low oxygen signal to activate genes essential for sugar and energy generation, ethylene and auxin biosynthesis, and root development under hypoxia. We also demonstrate HXK5/6-VDAC1 complex interacting with and inactivating CIPK15 on mitochondria in a sugar- and oxygen-dependent manner, revealing the structure-function relationship of CIPK15-HXK6-VDAC1 interaction. Under hypoxia, CIPK15 expression, phosphorylation and stability are enhanced, whereas expression of HXK5/6 and VDAC1 is reduced, thus enabling sufficient CIPK15 functionality to induce genes necessary for underwater root growth. Moreover, root-specific induction of CIPK15 prompted a 20-50% increase in grain yield in a hypoxic rice paddy. Our study reveals a unique mitochondria-based machinery in rice for sensing oxygen and promoting growth under hypoxia.
Rice seeds were sterilized in 3% (v/v) sodium hypochlorite for 1 h and washed with sterile deionized water. Seeds were laid on 1/2X MS agar (0.3% CultureGel™ Type1, Phytotechlab) medium without sucrose in 400 ml bottles filled with or without deionized water for submerged or aerobic treatments, respectively. Seeds were germinated at 28° C. under a 16:8 h light:dark cycle in a growth chamber. Water for submergence treatment was de-gassed with a vacuum pump and flushed with nitrogen before use. To examine root morphology, seeds were pre-germinated on 1/2X MS agar plates at 37° C. in the dark for 2 days, before transferring the seedlings to glass tubes (25 cm in height, 5 cm in diameter), with 5 seedlings per tube, for aerobic or submerged treatments in the growth chamber for another 12 days.
Setaria viridis seeds were sterilized in 0.6% (v/v) sodium hypochlorite plus 0.1% tween-20 for 10 minutes and washed with sterile deionized water. Seeds were laid on 1/2X MS agar medium without sucrose in glass jars and incubate at 4° C. for 2 weeks to break the dormancy, then the jars were shifted to a growth chamber setting at 24° C. under a 16:8 h light:dark cycle.
For inducible overexpression of CIPK15, full-length CIPK15 cDNA was inserted into pXVE:dHA vector between NotI and SpeI restriction sites, and then the plasmid was further inserted between KpnI and SpeI sites in pCAMBIA1301, generating pXVE:CIPK15-dHA. For CIPK15 promoter-driven GUS expression, the 2.0-kb CIPK15 promoter region plus the 1.4-kb 5′ untranslated region (UTR), including the first intron, was inserted into the pENTR™/D-TOPO™ vector (Invitrogen), generating pENTR-pCIPK15, and this plasmid was inserted into the binary vector pccdB:GUS/pSMY1H using the Gateway® LR system, generating pCIPK15:GUS. For LAX promoter-driven GUS expression, 2037-, 2629- or 2246-bp upstream of the ATG translation start codon, were inserted between EcoRI and NcoI sites of pCAMBIA1305.1, generating pLAX1:GUS, pLAX3:GUS and pLAX5:GUS, respectively.
To construct CIPK15:CIPK15, the CIPK15 promoter from pENTR-pCIPK15 was amplified with KpnI and NcoI restriction sites, and the coding region of CIPK15 was amplified with NcoI and SpeI restriction sites. The pCAMBIA1305.1 binary vector was then digested with KpnI and SpeI, allowing us to ligate the CIPK15 promoter and coding region, thereby generating the CIPK15:CIPK15 construct.
For plasmids used in our protoplast transient expression assays, cDNAs of CIPK15, HXK5, HXK6 and VDAC1 were inserted into pENTR vectors and then inserted into pUbi:ccdB-mCherry, pUbi:ccdB-GFP, p35S:cYFP-ccdB, p35S:ccdB-nYFP or pUbi:ccdB-HA binary vectors via the Gateway LR system, thereby generating CIPK15, HXK5 and HXK6 fused to desirable reporter genes.
The CIPK15 and HXK6 mutants were generated using pENTR-CIPK15 and pENTR-HXK6 as templates to construct different CIPK15 (ΔNAF, ΔPPi, T171D, T171A, NAF315-317PPP, L328P/F332P) and HXK6 (ΔTS, G112D, K203A) entry vectors by polymerase chain reaction (PCR) with specific primers and annealing with blunt-end ligation. pENTR:CIPK15ΔPPi was used as template for generating pENTR:CIPK15ΔPPi/Ti71D and pENTR:CIPK15ΔPPi/T171A. These entry vectors were inserted into pUbi:ccdB-mCherry or pUbi:ccdB-GFP binary vectors using the Gateway LR system.
For RNAi construction, the 3′ UTRs of HXK5 and HXK6 were used to generate pENTR-HXK5/6-3′UTR vectors, which were inserted into the pUbi:ccdB-GFPccdB-NosT vector via the Gateway LR system. The pUBQ10:CIPK15-mTagBFP construct was generated by amplifying CIPK15 cDNA and ligating it into the pGGM000 binary vector according to the instructions of the Greengate cloning system30.
To analyze aerenchyma area, seminal roots of 14-day-old seedlings were cross-sectioned at different positions from the root tip using a Microslicer™ (DTK-1000) vibrotome. Sections were stained with toluidine blue (Sigma-Aldrich) before capturing images under a microscope (Axioimager Z1, Carl Zeiss). The area of aerenchyma was determined in ImageJ software (Ver. 1.8.0, US National Institutes of Health).
Total mRNA was extracted from 5-day-old seedlings using the RNeasy Plant Mini Kit (Qiagen). RNA quality control and quantification were carried out using a Bioanalyzer 2100 system (Aligent). cDNA libraries were prepared with a TruSeq standard mRNA kit (Illumina) according to the manufacturer's instructions. cDNA sequencing was performed using a 500-high output v2 sequencing kit and an Illumina Nextseq500 instrument. Bioinformatics analysis was conducted in CLC Genomics Workbench software (v11.0.1, Qiagen).
Total RNA was extracted from roots of 14-day-old seedlings using Trizol reagent (Invitrogen) and treated with DNase I (Thermo Scientific) at 37° C. for 15 min. cDNA was synthesized from 1 μg of RNA using the Promega Reverse Transcription system and diluted 5-fold for further use. Real-time qRT-PCR was performed as described previously31.
Luciferase and GUS activity in transfected rice embryo calli were assessed as described previously32. GUS staining of rice seedlings was conducted as described previously33.
Plasmids pCIPK15:GUS and pXVE:CIPK15-dHA, as well as CIPK15:CIPK15, were introduced into Agrobacterium tumefaciens strain EHA105 and then rice transformation was performed as described previously 34. Plasmids OsCIPK15:OsCIPK15, were introduced into Agrobacterium tumefaciens strain EHA105 and then S. vridis transformation was performed as followed34.
Stems of 10-day-old rice seedlings were used to isolate protoplasts as described previously35. After transfection, protoplasts were cultured in 2 ml culturing medium in 6-well plates (Jet-Biofil) for 4 h on an orbital shaker at 60 rpm, and then divided into aerobic or submerged treatment groups. For aerobic treatment, protoplasts were kept under shaking in a 6-well plate. For submerged treatment, protoplasts in a 6-well plate were placed on the bench without shaking to keep the medium stagnant. All protoplasts were incubated at 25° C. in the dark for 12 h.
Fluorescence images were collected with a Zeiss LSM 780 confocal microscope. BFP, GFP/YFP and mCherry fluorescence images were detected with the laser line of excitation/emission at 405/415-470, 488/505-540 and 561/594-638 nm, respectively. Mitochondria were stained using Mitotracker™ Green FM (Thermo) for 15 min according to the manufacturer's instructions prior to examination under confocal microscopy.
Sources of antibodies: anti-HA antibody from Proteintech (66006-2-Ig), anti-tubulin antibody from Agrisera (AS20-4483), anti-GFP antibodies from GeneTex (GTX113617), anti-RFP antibody from ChromoTek (6G6), anti-GUS antibody from Sigma-Aldrich (G5420), and anti-CIPK15 antibody from Abbexa (abx018654). All antibodies were diluted 5000-fold before use. We conducted immunoblotting as described previously32.
Samples were extracted from rice protoplasts in lysis buffer containing 150 mM NaCl, 0.5% NP4-0, 20 mM Tris-HCl (pH 7.5), and protease inhibitor (Roche) for 1 h at 4° C. and centrifuged at 13,000 rpm for 30 min at 4° C. Supernatants were transferred to new tubes and GFP- or RFP-conjugated proteins were pulled down with GFP-Trap®_MA beads or RFP-Trap®_MA beads. Precipitated proteins were subjected to immunoblot analysis using anti-RFP and anti-GFP antibodies.
Two-day-old seedlings of the XVE: CIPK15-dHA and XVE:GFP-dHA (serving as control) transgenic lines were transplanted into 1/2X MS medium containing 5 □M β-estradiol for 5 days under aerobic or submerged conditions. Total proteins were extracted in lysis buffer containing 25 mM Tris-HCl (pH 7.5), 150 mM NaCl, 1% NP-40, 1 mM EDTA, 5% glycerol and protease inhibitor (Roche) and subjected to IP using Pierce™ Anti-HA Magnetic Beads to pull down HA-conjugated proteins. Eluted proteins were digested with trypsin before undergoing LTQ mass spectrometry-based proteomic analysis. CIPK15-interacting proteins were identified from XVE:CIPK15-dHA transgenic lines, but not from the control, under highly stringent criteria with a false discovery rate (FDR) of <1% for peptide identification. The peptide fragmentation data from LC-MS/MS were searched against RAP-DB (https://rapdb.dna.affrc.go.jp/) using MASCOT software (Matrix Science Ltd.).
Total proteins extracted from roots of the XVE:CIPK15-dHA transgenic line for IP-MS (described above) were used for phosphor-peptide mapping, as described previously31
To evaluate grain weight per plant in the field, 25-day-old seedlings were transplanted into soil, with 25×25 cm spacing between each plant, with a total of 10 plants of each line grown in the field and 15 plants of each line grown as one plot. Seeds were harvested after ripening, dried, and their weight per plant was determined as described previously33.
Five-day-old seedlings were treated with 2 or 5 mM of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) (Sigma) or [[concentration??]] the ACS inhibitor aminoethoxyvinylglycine (AVG) (Sigma) for 1 day.
Seedlings were grown under aerobic or hypoxic conditions for 7 days. Seminal roots were embedded in 5% agar, and positions at 1.5 cm above root tips were cross-sectioned at a 100-μm thickness using a vibratome Microslicer™ (DTK-1000) Vibrotome. Root sections were fixed with methanol. To examine lignin distribution, sections were stained with acriflavine as described previously (54) and imaged with a Zeiss LSM 780 confocal microscope using a 488 nm laser line for excitation and a 505 to 550 nm band pass filter for emission. To examine suberin lamellae, sections were stained with fluorol yellow 088 as described previously (55, 56) and imaged with a Zeiss LSM 780 confocal microscope using an excitation wavelength of 488 nm and 524 to 594 nm for emission.
Luciferase activity in protoplasts transfected with the reporter construct alone was set to 1, and other values in protoplasts transfected with both effector and reporter constructs were calculated relative to this value (relative values are shown above bars in bar plots). Error bars indicate the SE or SD from three independent experiments. *, ** and *** represent significance levels of P<0.05, 0.01 and 0.001, respectively, according to Student's t-test. n.s. indicates no significant difference. For bar plots displaying letters above the bars, statistical analysis was performed by one-way ANOVA with a post-hoc Tukey HSD. Significant levels are labeled at p<0.05.
We grew seedlings of wild type (WT) (cv. Nipponbare) and cipk15 knockout mutant plants (
Aerenchyma development facilitates vertical O2 transmission and enhances hypoxia tolerance, and it is an important indicator of active root growth15. We observed that aerenchyma and root development were retarded in 14-day-old cipk15 seedlings maintained under aerobic conditions and they were almost completely inhibited under hypoxia compared to WT (
We performed an RNA sequencing (RNA-seq) analysis on WT and cipk15 mutant lines to identify genes regulated by CIPK15 under hypoxia. Apart from genes known to be involved in sugar production and metabolism in post-germination seedlings, we uncovered many genes involved in ethylene biosynthesis and signaling and aerenchyma development that were downregulated in the cipk15 line (
qRT-PCR analysis validated that levels of the ACS1, EIN3/EIN1 and CEL mRNAs were all increased in WT under hypoxia, but they were increased to a lesser extent under hypoxia in cipk15 (
To confirm that CIPK15 regulates aerenchyma and root development through the ethylene-dependent pathway, rice seedlings were cultured in medium with or without ethephon under submergence. Ethephon can be converted to ethylene upon dissolving in water. We found that cipk15 seedlings grew more slowly than WT without ethephon, but faster with ethephon treatment (
CIPK14 and CIPK15 in the rice genome are highly homologous, with only a few nucleotide and amino acid differences in the cDNA and protein sequences, respectively, so qRT-PCR-based differentiation of the expression of these two genes is problematic. An RNA-seq analysis indicated that transcript levels are similar for CIPK14 and CIPK15, with only the CIPK15 transcript being abolished in the cipk15 line under both aerobic and hypoxic conditions (
Under hypoxia, post-germination seedling development can be divided into two stages, i.e., germination/coleoptile elongation (days 1-4) and leaf/root development (days 5-7) in WT rice. However, this process was delayed in cipk15, with only coleoptile elongation being observed up to day 7 (
αAmy3 is a highly sensitive gene to sugar starvation and hypoxia2,7, and ACS is generally considered as responsible for the rate-limiting step in ethylene biosynthesis38. Therefore, we have used αAmy3 and ACS1 promoters as markers of CIPK15-activated sugar starvation and ethylene-responsive pathways, respectively. Here, we co-transfected rice suspension cells with Ubi:CIPK15 (effector) and ACS1:LUC or αAmy3:LUC (reporters) and incubated them with or without glucose under aerobic or hypoxic conditions. We found that CIPK15-activated αAmy3 and ACS1 promoter activities were lowest in the presence of both sugar and O2, increased under either sugar starvation or hypoxia, and were highest under a combination of both sugar starvation and hypoxic conditions Thus, CIPK15 is induced by sugar starvation and hypoxia in a developmentally-regulated biphasic pattern that sequential activates genes necessary for starch-to-sugar conversion and low-level ethylene production during germination/coleoptile development, as well as for high-level ethylene production during leaf and root development under hypoxia (
We observed that grain yields of cipk15 mutant plants grown in a rice paddy with regular irrigation were significantly lower than WT (
2.4 HXK 5/6 and VDAC1 Interact with CIPK15 and Suppress its Activity on Mitochondria
To identify proteins that interact with CIPK15 and regulate its activity, we extracted total proteins from roots of β-estradiol-treated XVE: CIPK15-dHA transgenic plants grown under aerobic or hypoxic conditions and subjected them to co-immunoprecipitation (co-IP) and proteomics analyses. CIPK15-interacting proteins with top Mascot scores >200 are collected. Most of these proteins were pulled down by CIPK15 under both aerobic and hypoxic conditions, except for HXK5 and HXK6 that were pulled down by CIPK15 only under the aerobic condition.
To explore these latter interactions in vivo using co-IP assays, we co-transfected rice protoplasts with Ubi:CIPK15-mCherry and Ubi:HXK5-GFP, Ubi:HXK6-GFP or Ubi:GFP (negative control) constructs. Then, total proteins were extracted before isolating the CIPK15-mCherry protein complex. Our anti-RFP antibodies detected CIPK15-mCherry proteins in all eluents of CIPK15-mCherry co-IP fractions, but anti-GFP antibodies detected HXK5-GFP and HXK6-GFP present in the CIPK15-mCherry complex (
We also performed a bimolecular florescence complementation (BiFC) assay by co-transfecting rice protoplasts with CaMV35S:cYFP-CIPK15 and CaMV35S:HXK5/6-nYFP, which revealed that CIPK15 interacts with HXK5 and HXK6 at mitochondria (
In rice protoplast transient expression assays, the αAmy3 and ACS1 promoters were significantly induced upon overexpression of CIPK15, HXK5-Ri and HXK6-Ri, but they were suppressed by overexpression of HXK5 or HXK6 (
We also examined other proteins and found that only VDAC1 was predicted to be associated with mitochondria. In a co-IP assay of rice protoplasts co-transfected with Ubi:VDAC1-GFP, Ubi:CIPK15-HA and Ubi:HXK6-GFP or Ubi:HXK6:mCherry, it was revealed that VDAC1 interacted with both HXK6 and CIPK15 (
In Arabidopsis and rice, the sugar catabolism and sensing activities of HXKs can be uncoupled23,39. Amino acid residues Gly112 (G112) and Lys203 (K203) in rice HXK6 are essential for glucose phosphorylation and glucose binding, respectively40 (
We obtained a T-DNA-inserted hxk6 mutant and found that the hxk6 homozygous variant was lethal, with only the heterozygous mutant surviving, indicating that HXK6 is indispensable for plant growth. No difference in root growth between the heterozygous mutant and WT was detected under aerobiosis, but root growth was faster for the mutant than for WT under hypoxia (
2.6 the NAF Domain is Essential for CIPK15 Activity, Mitochondrial Localization and Interaction with HXK6.
The CIPK family is typically composed of an N-terminal catalytic/kinase domain containing an activation loop, and a C-terminal regulatory domain containing the autoinhibitory Asn-Ala-Phe (NAF) domain, with the NAF domain directly interacting with the catalytic domain to inhibit kinase activity41. To define the functional domains in CIPK15 (
The NAF domain of the CIPK protein family comprises 23-24 amino acids in Arabidopsis and rice, and it contains several highly conserved hydrophobic amino acids (
HXK6 (K203A) that lacks glucose-binding activity cannot suppress CIPK15 activity (
2.7 OsCIPK15:CIPK15 Improves Flooding Tolerance in S. viridis
Above findings demonstrated that OsCIPK15 is essential for the germination and root development under hypoxia in rice. To test whether OsCIPK15 is also able to confer flooding tolerance to other cereals, we transformed the plasmid OsCIPK15:OsCIPK15 into a flooding-intolerance species: S. viridis. Our results showed that, under aerobic conditions, the WT (cv. ME034V) exhibited shorter primary roots, and almost no aerenchyma development, whereas transgenic plants had longer roots and more aerenchyma along its primary roots. (
qRT-PCR analysis showed that OsCIPK15 was significantly induced under hypoxia in two transgenic plants, but almost undetectable in the WT. SevCIPK15 expressions were also induced by hypoxia, and could be further induced in the OsCIPK15 transgenic plants, suggesting a possible positive feedback regulation by OsCIPK15. The expression of SevACS1 was similar to that of OsCIPK15, which was induced by hypoxia and showed higher expression in the transgenic plants (
In addition, to uncover the unique features of OsCIPK15, we compared the protein sequences from OsCIPK15 with those of its orthologues from other Poaceae cereals. Alignment results showed that Ile-48 from OsCIPK15 is uniquely present in the Oryza genus, the other ortholog proteins containing Val-48 (
Plant root architecture and function are essential aspects of water and nutrient uptake, anchorage, and interactions with microbes in soil, all of which are related to processes that impact growth rate, abiotic stress tolerance and productivity. Underwater root growth is critical to plants surviving flooding conditions. Here, we have deciphered a unique mechanism employed by rice for hypoxia tolerance. We show that the mitochondria-associated CIPK15-HXK5/6-VDAC1 complex regulates carbohydrate metabolism, ethylene and auxin biosynthesis/transport, root anatomy, and root development for flooding adaptation in rice, ultimately improving grain yield in a rice paddy.
Two unique features enable CIPK15 to play a key role in flooding tolerance in rice. First, CIPK15 regulates ethylene biosynthesis in roots under hypoxia. Ethylene is produced by all plant cells and, as a gas, it quickly diffuses and is sensed at production sites. Due to restricted gas diffusion and O2 exchange under water, ethylene concentrations increase rapidly in submerged plant tissues, initiating ethylene signaling to regulate genes responsive to flooding42. The mechanisms by which ethylene biosynthesis is regulated under hypoxia had previously been unclear. In rice, increased expression of CUT1-LIKE (CUT1L, a homolog of CUT1 required for cuticular wax production in Arabidopsis) induces accumulations of very-long-chain fatty acids, and REDUCED CULM NUMBER (RCN1, an ATP-binding cassette transporter) enhances ACS1 and ACO5 expression, both of which serve to promote ethylene accumulation and aerenchyma formation in rice roots under hypoxia43. We found that CIPK15 upregulates ACS, ACO, CUT1L and RCN1 expression in rice seedlings under hypoxia (
Second, CIPK15 senses sugar and O2 deficiency and reprograms plant metabolism and development to adapt to flooding. As seedlings develop, the expression and function of CIPK15 itself is regulated by sugar starvation and hypoxia in a developmentally-regulated biphasic pattern (
A previous phylogenetic analysis revealed that CIPK14/15 in rice formed a clade distinct from other CIPKs in rice and Arabidopsis41, implying that rice CIPK15 may exert unique functions different from those of other CIPKs. Our study demonstrates that the core Asn-Ala-Phe amino acids in the NAF domain are necessary for CIPK15 activity and association with mitochondria and HXK6. In Arabidopsis, CBL-CIPK interaction controls transport of various ions across the plasma and vacuolar membranes46, and the NAF domain of CIPK is responsible for interacting with CBL and also serves as a kinase autoinhibitory region 47.
VDAC, a mitochondrial porin, is the most abundant protein of the mitochondrial outer membrane and is the major channel for the exchange of metabolites and ions between mitochondria and other cellular compartments29. In animal cells, VDAC1 interacts with partner proteins to regulate mitochondrial functions. Binding of VDAC1 to HXK provides a metabolic benefit and apoptosis-suppressive capacity to many cancer cells that endows them with a proliferative advantage and increased resistance to chemotherapy 28. The N-terminal region (residues 1-15) of animal HXKII is required for its mitochondrial localization and interaction with VDAC129. We demonstrate herein that rice VDAC1 interacts and cooperates with HXK6 to suppress CIPK15 activity (
In WT rice, transcript levels of CIPK15 increased by ˜24% under hypoxia compared to aerobic conditions (
CIPK15 is required for aerenchyma and root development, as revealed by aerenchyma area being significantly reduced (
HXKs catalyze the ATP-dependent phosphorylation of glucose to glucose-6-phosphate. A previous protein structure-based study demonstrated that rice HXK6 adopts an open inactive state in the absence of glucose, but is rearranged into a closed active state upon binding glucose40. We show herein that glucose binding, likely a closed yet active state, but not the phosphorylation of glucose by HXK6, suppresses CIPK15 activity. HXK5 and HXK6 share similar features, e.g., localization on mitochondria, interaction with CIPK15, and suppression on CIPK15 activity. HXK5 is a major HXK functioning during pollen germination and tube growth, with HXK5 knockout mutant plant being able to grow yet male sterile48. In the present study, the HXK6 homozygous knockout mutant seedling is unable to grow, indicating HXK6 is necessary for hexose metabolism during plant growth.
Accordingly, we propose a model to illustrate the function of the HXK6-CIPK15-VDAC1 interaction on mitochondria and how it regulates glucose-dependent rice root development. Glucose-bound HXK6 adopts a closed state that suppresses CIPK15 activity (
In summary, the elevated O2 concentrations associated with well-drained soil allow HXK5/6-VDAC1 to accumulate and suppress CIPK15 activity, leading to maintenance of minimal levels of active CIPK15 on mitochondria, low ethylene accumulation, and constitutive aerenchyma development (
Rice bears unique features that have permitted it to adapt to hypoxic environments. OsCIPK15 is the key gene that is essential for anaerobic germination and hypoxic root growth. In this chapter, we report the first successful case of conferring flood tolerance to a flooding-sensitive species into tolerant by transforming rice OsCIPK15 into S. viridis.
The root architecture of S. viridis differs from that of rice, which lacks of sclerenchyma49, and carries fewer layers of cortex50. To date, no studies have described aerenchyma formation in S. viridis, but studies examining the acclimated species Setaria italica have shown that it exhibits low level of aerenchyma development compared to other waterlogging-tolerant-speciessis51,52. We demonstrated that seminal roots were longer in OsCIPK15 transgenic lines than the seminal roots in the WT (
Underwater seedling development can be classified into coleoptile elongation and shoot/root development stages (
The importance of ethylene accumulation to underwater seedling development has been previously described53. In previous chapters, we have shown that OsCIPK15 is the key regulator for the ethylene biosynthesis in rice in previous chapters. Here, we further demonstrate that the expression profiles of OsCIPK15 are correlated with the expression of SevACS1 and the phenotypes of S. viridis. OsCIPK15-7 showed the highest expression level of OsCIPK15, and also exhibited the best seedling growth under hypoxia, while OsCIPK15-8 expressed mild levels of OsCIPK15 and SevACS1, remaining at the coleoptile elongation stage at 14 DAI under hypoxia (
Our sequence alignment results suggested that CIPK15 is highly conserved across the Poaceae family, showing >80% similarity among the orthologue proteins (
In summary, our study demonstrated that OsCIPK15 can confer flooding tolerance in other species. We showed that OsCIPK15 carries the amino acid residue Ile-48, which allows it to regulate ethylene-dependent aerenchyma development. To date, no other studies have successfully improved underwater seedling development in a plant species other than rice. Our study offers an important strategy for improvement of flooding tolerance in plants, and also reveals a new insight into how rice possesses superior flooding tolerance under an evolutionary lens.
This application claims the benefit of U.S. provisional application No. 63/497,834, filed Apr. 24, 2023 under 35 U.S.C. § 119, the entire content of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 63497834 | Apr 2023 | US |
