Genes for enhancing drought and heat tolerance in plants and methods of use
The present disclosure provides methods for increasing drought resistance and heat resistance of a plant. The methods encompass expression of at least one heat shock protein (HSP) from the group consisting of HSP40, HSP60 or HSP70 together with a phosphoenolpyruvate carboxylase (PEPC) comprising an aspartic acid (D) at a position that corresponds to the position 509 of SEQ ID NO: 4, in the plant. In comparison to a plant not manipulated in this manner, the disclosed, genetically-modified, plants display improved drought resistance and heat resistance. Also provided are plants that can be obtained by the method according to the invention, and nucleic acid vectors to be used in the described methods.
1. A method of improving drought and heat tolerance in a plant or plant cell, comprising introducing into the plant or plant cell an exogenous nucleic acid encoding at least one heat shock protein (HSP) selected from the group consisting of HSP40, HSP60 and HSP70, and further expressing in the plant an exogenous nucleic acid encoding a phosphoenolpyruvate carboxylase (PEPC) comprising an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
2. A method of improving drought and heat tolerance in a plant or plant cell, comprising introducing into the plant or plant cell an exogenous nucleic acid encoding at least one heat shock protein (HSP) selected from the group consisting of HSP40, HSP60 and HSP70, and further expressing an exogenous nucleic acid encoding a phosphoenolpyruvate carboxylase (PEPC) of a CAM plant species selected from the group consisting of genera Kalanchoe Phalaenopsis, Ananas and Crassula.
3. A method of improving drought and heat tolerance in a plant or plant cell, comprising introducing into the plant or plant cell an exogenous nucleic acid encoding at least one heat shock protein (HSP) selected from the group consisting of HSP40, HSP60 and HSP70, and further introducing a mutation into an endogenous phosphoenolpyruvate carboxylase (PEPC) gene wherein the resulting mutated gene encodes a PEPC comprising an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
4. The method of claim 3 , wherein the mutation is introduced by genome editing, which is achieved by a method selected from the group consisting of CRISPR/Cas system, Cre/Lox system, TALEN system, ZFNs system and homologous recombination.
5. The method of claim 4 , wherein said CRISPR/Cas system comprises introducing into the plant or plant cell a first nucleic acid encoding a Cas9 or Cas12 nuclease, a second nucleic acid comprising a guide RNA (gRNA), and a third nucleic acid comprising a homologous repair template of a PEPC gene wherein the third nucleic acid encodes an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
6. The method of claim 1 , wherein the exogenous nucleic acid encoding at least one HSP is expressed during daytime and the nucleic acid encoding PEPC is expressed during night time.
7. The method of claim 1 , wherein the exogenous nucleic acid encoding at least one HSP and nucleic acid encoding PEPC are expressed constitutively.
8. The method of claim 1 , wherein the exogenous nucleic acid encoding at least one HSP is stably transfected or transformed into the plant or plant cell genome.
9. The method of claim 1 , wherein the exogenous nucleic acid encoding at least one HSP is expressed in the leaf tissue.
10. The method of claim 1 , wherein the plant is a C3 plant selected from the group consisting of genera Allium, Arabidopsis, Brassica, Capsicum, Citrullus, Cucumis, Eucalyptus, Fragaria, Glycine, Gossypium, Hordeum, Ipomoea, Malus, Manihot, Nicotiana, Oryza, Populus, Prunus, Rosa, Solanum, Spinacia and Triticum.
11. The method of claim 1 , wherein the plant is a C4 plant selected from the group consisting of genera Panicum, Saccharum, Setaria, Sorghum and Zea.
12. The method of claim 1 , wherein at least two of the HSP40, HSP60 and HSP70 are expressed simultaneously in the plant or plant cell.
13. A genetically modified plant or plant cell produced by the method of claim 1 .
14. A genetically-modified plant or plant cell, wherein the plant or plant cell is modified to express an exogenous nucleic acid encoding at least one heat shock protein (HSP) selected from the group consisting of HSP40, HSP60 and HSP70, and wherein the plant or plant cell is further modified to express a nucleic acid encoding a phosphoenolpyruvate carboxylase (PEPC) comprising an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
15. The genetically-modified plant or plant cell of claim 14 , wherein the PEPC is expressed from the endogenous PEPC gene mutated to encode an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
16. The genetically-modified plant or plant cell of claim 14 , wherein the exogenous nucleic acid encoding at least one HSP is expressed during daytime and the nucleic acid encoding PEPC is expressed during night time.
17. The genetically-modified plant or plant cell of claim 14 , wherein the plant is a C3 plant or a C4 plant selected from the group consisting of genera Allium, Arabidopsis, Brassica, Capsicum, Citrullus, Cucumis, Eucalyptus, Fragaria, Glycine, Gossypium, Hordeum, Ipomoea, Malus, Manihot, Nicotiana, Oryza, Populus, Prunus, Rosa, Solanum, Spinacia, Triticum, Panicum, Saccharum, Setaria, Sorghum , and Zea.
18. An expression vector, comprising a nucleotide sequence operably linked to a regulatory region that is functional in a plant or plant cell, wherein the nucleotide sequence encodes a heat shock protein (HSP) selected from the group consisting of HSP40, HSP60, HSP70, and a phosphoenolpyruvate carboxylase (PEPC) comprising an aspartic acid (D) at a position corresponding to position 509 of SEQ ID NO: 4.
19. The expression vector of claim 18 , wherein the expression vector directs temporally controlled expression of the nucleotide sequence.
20. The expression vector of claim 19 , wherein the temporally controlled expression comprises gene expression during nighttime.
21. The expression vector of claim 19 , wherein the temporally controlled expression comprises gene expression during daytime.
22. The expression vector of claim 18 , wherein the regulatory region comprises a promoter selected from the group consisting of a constitutive promoter, a tissue-specific promoter, and a regulated promoter.
23. The expression vector of claim 22 , wherein the tissue-specific promoter is a leaf-specific promoter.
24. The expression vector of claim 23 , wherein the leaf-specific promoter is selected from the group consisting of a ribulose-1,5-bisphosphate carboxylase/oxygenase (RbcS) promoter, a chlorophyll a/b binding-6 (cab6) promoter, a chlorophyll a/b binding-1(Cab-1) promoter, a cab IR promoter from rice, a pyruvate orthophosphate dikinase (PPDK) promoter, a light-harvesting complex of photosystem (Lhcb1*2) promoter, a sucrose-H+ symporter (SUC2) promoter and a thylakoid membrane protein promoter.
25. The expression vector of claim 22 , wherein the constitutive promoter is selected from the group consisting of a ubiquitin promoter, a cauliflower mosaic virus (CaMV) 35S promoter, a nopaline synthase (nos) promoter, an actin promoter, a peanut chlorotic streak caulimovirus promoter, a Chlorella virus methyltransferase gene promoter, a full-length transcript promoter form figwort mosaic virus, a pEMU promoter, a MAS promoter, a maize H3 histone promoter and an Agrobacterium gene promoter.
26. The expression vector of claim 22 , wherein the regulated promoter is selected from the group consisting of a stress induced promoter, a chemical-induced promoter, a light induced promoter, a dark-induced promoter, and a circadian-clock controlled promoter.
27. A method for improving drought and heat tolerance in a plant or plant cell, comprising introducing the expression vector of claim 18 into a plant or plant cell, and expressing the nucleotide sequence in the plant or plant cell.
28. A plant or plant cell comprising the expression vector of claim 18 .