Method for making nicotiana plants with mutations in XylT and FucT alleles using rare-cutting endonucleases
Materials and methods are provided for making plants (e.g., Nicotiana varieties) that are suitable for producing therapeutic polypeptides suitable for administration to humans and animals, particularly by making TAL effector endonuclease-induced mutations in genes encoding xylosyltransferases and fucosyltransferases.
1. A method for making a Nicotiana benthamiana plant that comprises a mutation in each of a plurality of XylT1 and XylT2 alleles and a mutation in each of a plurality of FucT1 and FucT2 alleles, said method comprising:
(a) contacting a population of Nicotiana benthamiana plant cells comprising functional XylT1 and XylT2 alleles and functional FucT1 and FucT2 alleles with a single TAL effector endonuclease that binds to a first pair of nucleic acid sequences selected from the group consisting SEQ ID NOs: 47 and 48, SEQ ID NOs: 49 and 50, and SEQ ID NOs: 51 and 52, each of said first pair of nucleic acid sequences located in the plurality of XylT1 and XylT2 alleles, and a second TAL effector endonuclease that binds to a second pair of nucleic acid sequences selected from the group consisting SEQ ID NOs: 53 and 54, SEQ ID NOs: 55 and 56, SEQ ID NOs: 57 and 58, SEQ ID NOs: 58 and 59, and SEQ ID NOs: 62 and 63, each of said second pair of nucleic acid sequences located in the plurality of FucT1 and FucT2 alleles, wherein said Nicotiana benthamiana plant cells are protoplasts,
(b) selecting, from said population, a cell in which each of said plurality of XylT1 and XylT2 alleles and each of said plurality of FucT1 and FucT2 alleles have been inactivated, and
(c) regenerating said selected plant cell into athe Nicotiana benthamiana plant, wherein said selected Nicotiana benthamiana plant does not produce detectable levels of beta-1,2-xylosyl-sugars and produces reduced levels of core alpha-1,3-fucosyl-sugars on N-glycan structures of glycoproteins compared to a corresponding plant that does not contain said mutations.
2. The method of claim 1 , comprising isolating genomic DNA comprising at least a portion of a XylT locus or at least a portion of a FucT locus from said protoplasts.
3. A method for making a Nicotiana benthamiana plant that comprises a mutation in one or more XylT1 and XylT2 alleles and a mutation in one or more FucT1 and FucT2 alleles, said method comprising:
(a) contacting a population of Nicotiana benthamiana plant cells comprising functional XylT1 and XylT2 alleles and functional FucT1 and FucT2 alleles with a first TAL effector endonuclease that binds to a first pair of nucleic acid sequences selected from the group consisting SEQ ID NOs: 47 and 48, SEQ ID NOs: 49 and 50, and SEQ ID NOs: 51 and 52, each of said first pair of nucleic acid sequences located in the plurality of XylT1 and XylT2 alleles, and a second TAL effector endonuclease that binds to a second pair of nucleic acid sequences selected from the group consisting SEQ ID NOs: 53 and 54, SEQ ID NOs: 55 and 56, SEQ ID NOs: 57 and 58, SEQ ID NOs: 58 and 59, and SEQ ID NOs: 62 and 63, each of said second pair of nucleic acid sequences located in the plurality of FucT1 and FucT2 alleles,
(b) selecting, from said population, a cell in which one or more XylT1 and XylT2 alleles and one or more FucT1 and FucT2 alleles have been inactivated, and
(c) regenerating said selected plant cell into the Nicotiana benthamiana plant, wherein the levels of beta-1,2-xylosyl- and core alpha-1,3-fucosyl-sugars on N-glycan structures of glycoproteins produced in said plant are decreased as compared to a corresponding plant that does not contain said mutations.
4. The method of claim 3 , comprising transforming said protoplasts with one or more vectors encoding said TAL effector endonucleases.
5. The method of claim 3 , comprising introducing into said protoplasts a nucleic acid encoding a TAL effector endonuclease protein.
6. The method of claim 1 , wherein said Nicotiana benthamiana plant comprises a deletion in each XylT1 and XylT2 allele and a deletion in each FucT1 and FucT2 allele.
7. The method of claim 1 , wherein said first TAL effector endonuclease binds to SEQ ID NOS:51 and 52, and wherein said second TAL effector endonuclease binds to SEQ ID NOS:58 and 59.
8. The method of claim 3 , wherein said first TAL effector endonuclease binds to SEQ ID NOS:51 and 52, and wherein said second TAL effector endonuclease binds to SEQ ID NOS:58 and 59.