Compositions and methods for producing plants resistant to glyphosate herbicide
The present disclosure includes the production of a mutant plant resistant to an herbicide of the phosphonomethylglycine family, e.g. glyphosate. Compositions and methods are provided for editing a nucleotide sequence of interest in a cell employing a guide polynucleotide/Cas endonuclease system, wherein the Cas endonuclease is guided by a guide polynucleotide to recognize and optionally introduce a double strand break at a specific target site into the genome of a cell. The nucleotide sequence of interest to be edited can be located within or outside the target site that is recognized by a Cas endonuclease. More specifically, compositions and methods are provided for editing an enolpyruvylshikimate-3-phosphate synthase (EPSPS) nucleotide sequence in a cell. The methods and compositions employ a guide polynucleotide/Cas endonuclease system to provide for an effective system for editing EPSPS nucleotide sequences of within the genome of a cell. Also provided are compositions and methods for the production of glyphosate tolerant plant cells, plants explants, seeds and grain.
1. A method for producing an enolpyruvylshikimate-3-phosphate synthase (EPSPS) mutant plant, the method comprising:
a) providing to a plant cell comprising an EPSPS nucleotide sequence operably linked to a heterologous regulatory element a guide RNA, a polynucleotide modification template comprising at least one nucleotide modification of the EPSPS nucleotide sequence, and a Cas endonuclease, wherein said guide RNA and Cas endonuclease are capable of forming a complex that enables the Cas endonuclease to introduce a double strand break at a target site in the genome of said plant cell, and wherein the at least one nucleotide modification comprises a TIPS modification;
b) obtaining a plant from the plant cell of (a);
c) evaluating the plant of (b) for the presence of said at least one nucleotide modification; and,
d) selecting a progeny plant that shows resistance to glyphosate.
2. A method for producing an enolpyruvylshikimate-3-phosphate synthase (EPSPS) mutant plant, the method comprising:
a) providing to a plant cell comprising an EPSPS nucleotide sequence a guide RNA, a polynucleotide modification template comprising at least one nucleotide modification of the EPSPS nucleotide sequence, and a Cas endonuclease, wherein said guide RNA and Cas endonuclease are capable of forming a complex that enables the Cas endonuclease to introduce a double strand break at a target site in the genome of said plant cell, and wherein the at least one nucleotide modification comprises a TIPS modification and a promoter replacement;
b) obtaining a plant from the plant cell of (a);
c) evaluating the plant of (b) for the presence of said at least one nucleotide modification; and,
d) selecting a progeny plant that shows resistance to glyphosate.
3. The method of claim 1 , wherein the at least one nucleotide modification further comprises a modification selected from the group consisting of (i) a nucleotide modification resulting in a lysine to arginine substitution (K90R) at the amino acid position corresponding to residue 90 of the maize EPSPS amino acid sequence, (ii) insertion of an intron mediated enhancer element (IME), or combinations thereof.
4. The method of claim 2 , wherein the at least one nucleotide modification further comprises a modification selected from the group consisting of (i) a nucleotide modification resulting in a lysine to arginine substitution (K90R) at the amino acid position corresponding to residue 90 of the maize EPSPS amino acid sequence, (ii) insertion of an intron mediated enhancer element (IME), or combinations thereof.
5. A method for producing an enolpyruvylshikimate-3-phosphate synthase (EPSPS) mutant plant, the method comprising:
a) providing to a plant cell comprising an EPSPS nucleotide sequence comprising a TIPS modification a guide RNA, a polynucleotide modification template comprising at least one nucleotide modification of the EPSPS nucleotide sequence, and a Cas endonuclease, wherein said guide RNA and Cas endonuclease are capable of forming a complex that enables the Cas endonuclease to introduce a double strand break at a target site in the genome of said plant cell, and wherein the at least one nucleotide modification comprises a promoter replacement;
b) obtaining a plant from the plant cell of (a);
c) evaluating the plant of (b) for the presence of said at least one nucleotide modification; and,
d) selecting a progeny plant that shows resistance to glyphosate.
6. The method of claim 5 , wherein the at least one nucleotide modification further comprises a modification selected from the group consisting of (i) a nucleotide modification resulting in a lysine to arginine substitution (K90R) at the amino acid position corresponding to residue 90 of the maize EPSPS amino acid sequence, (ii) insertion of an intron mediated enhancer element (IME), or combinations thereof.
7. The method of claim 1 , wherein the plant is soybean or maize.
8. The method of claim 2 , wherein the plant is soybean or maize.
9. The method of claim 5 , wherein the plant is soybean or maize.