Methods for efficient maize genome editing
The invention relates to novel maize plants, seeds and compositions, as well as improvements to maize plant breeding and methods for creating modifications in maize plant genomes.
1. A method of effecting in a Zea sp. nuclear genome at least one targeted modification of a first predetermined target site in a promoter region upstream of a transcription start site of a first gene and at least one targeted modification of a second predetermined target site in a promoter region upstream of a transcription start site of a second gene, wherein the targeted modifications result in a change of expression in the first gene and a change of expression in the second gene, wherein the targeted modifications comprise an insertion of a predetermined sequence encoded by a single stranded DNA polynucleotide donor molecule that does not have homology arms, wherein each targeted modification is achieved by integrating the predetermined sequence at a double-strand break (DSB) in the first and the second predetermined target sites by non-homologous end joining (NHEJ), wherein the predetermined sequence is integrated about 50 to about 500 nucleotides 5′ to the start codon of the coding sequence of the first and second gene, and wherein the predetermined sequence encoded by the single-stranded DNA polynucleotide donor molecule comprises a transcription factor recognition site sequence, thereby modifying the nuclear genome.
2. The method of claim 1 , wherein the DSB is introduced into the Zea sp. genome by at least one of the group consisting of:
(a) a nuclease selected from the group consisting of an RNA-guided nuclease, an RNA-guided DNA endonuclease, a type II Cas nuclease, a Cas9, a type V Cas nuclease, a Cpf1, a CasY, a CasX, a C2c1, a C2c3, an engineered nuclease, a codon-optimized nuclease, a zinc-finger nuclease (ZFN), a transcription activator-like effector nuclease (TAL-effector nuclease), an Argonaute, and a meganuclease or engineered meganuclease;
(b) a polynucleotide encoding one or more nucleases capable of effecting site-specific alteration of a target nucleotide sequence; and
(c) a guide RNA (gRNA) for the RNA-guided nuclease, or DNA encoding a gRNA for the RNA-guided nuclease.
3. The method of claim 2 , wherein the DSB is introduced by (a) a RNA-guided nuclease or DNA encoding an RNA-guided nuclease and (b) a gRNA or DNA encoding a gRNA, which are introduced into the Zea sp. nuclear genome by contacting with particles or nanoparticles.
4. The method of claim 1 , wherein the change of expression in the first gene and the change of expression in the second gene are both associated with improvement, relative to a reference Zea sp. genome lacking the targeted modifications, in resource partitioning.
5. The method of claim 1 , wherein the sequence encoded by the single-stranded DNA polynucleotide donor molecule that is integrated into the double-strand break (DSB) located in the promoter region upstream of the transcription start site of the first gene, is identical to the sequence encoded by the single-stranded DNA polynucleotide donor molecule that is integrated into the double-strand break (DSB) located in the promoter region upstream of the transcription start site of the second gene.
6. The method of claim 4 , wherein the first gene is associated with nitrogen utilization and the second gene is associated with nitrogen transport.
7. The method of claim 6 , wherein the first gene associated with nitrogen utilization is a gene encoding a protein in the glutamine synthetase (GS) enzyme family.
8. The method of claim 4 , wherein the first gene has a DNA sequence that is at least 90% identical to SEQ ID NO: 683 or SEQ ID NO: 685, or that encodes a protein that has an amino acid sequence that is at least 90% identical to an amino acid sequence of SEQ ID NO: 684 or SEQ ID NO: 686.
9. The method of claim 4 , wherein the first gene is a gene encoding a protein in the glutamine synthase enzyme family and the second gene is a transcription factor Dof1 gene and wherein the targeted modifications result in increased expression of the first and second genes, relative to expression in a reference cell lacking the modifications.
10. The method of claim 4 , wherein the first gene is a Gln1.3 gene and the second gene is a Dof1 gene, and wherein the targeted modifications result in increased expression of the first and second genes, relative to expression in a reference cell lacking the modifications.
11. The method of claim 4 , wherein the predetermined sequence encoded by a single-stranded DNA polynucleotide donor is a nitrogen-responsive element sequence.
12. The method of claim 4 , wherein the predetermined sequence encoded by a single-stranded DNA polynucleotide donor comprises at least one auxin-responsive element sequence.
13. The method of claim 1 , wherein the predetermined sequence comprises SEQ ID NO: 343.