Methods and compositions for generating dominant alleles using genome editing
AssigneeMonsanto Technology LLC
InventorsEdward James Cargill, Douglas Michael Eudy, Andrei Y. Kouranov, Richard Joseph Lawrence, Thomas L. Slewinski, Randy Shultz, PokChun Jennifer To, Samuel Sukhwan Yang, Yuanji Zhang
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Abstract
The present disclosure provides methods and compositions for generating dominant alleles using targeted editing techniques. Also provided are modified chromosomes, cells, tissues, and plants comprising modified dominant allele.
Claims6
A method of generating a dominant negative allele of a gene in a cell comprising inverting a portion of the gene using a targeted editing technique, wherein the inversion results in the production of an antisense RNA transcript under the control of the native promoter of the gene, wherein the antisense RNA transcript is capable of triggering suppression of an unmodified allele of the gene, wherein the dominant negative allele is not exogenously introduced, wherein the gene is a GA20 oxidase gene, and wherein the GA20 oxidase gene is encoded by an mRNA that encodes a protein having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NO:
- 30 and SEQ ID NO:
- 35.
A method of generating a dominant negative allele of a gene in a cell comprising inverting a portion of the gene using a targeted editing technique, wherein the inversion results in the production of an antisense RNA transcript under the control of the native promoter of the gene, wherein the antisense RNA transcript is capable of triggering suppression of an unmodified allele of the gene, wherein the dominant negative allele is not exogenously introduced, and wherein the unmodified allele comprises a polynucleotide sequence having at least 95% identity or complementarity to a sequence selected from the group consisting of SEQ ID NOs:
- 1, 12, 27, 28, 29, 31, 32 and 33.
A method of generating a dominant negative allele of a first gene in a cell comprising deleting a second gene with a native promoter that is positioned in the opposite orientation relative to the first gene using a targeted editing technique, wherein the deletion results in the production of an antisense RNA transcript of the first gene under the control of the native promoter of the second gene, wherein the dominant negative allele is not exogenously introduced, wherein the first gene is a GA20 oxidase gene, and wherein the GA20 oxidase gene is encoded by an mRNA that encodes a protein having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NO:
- 30 and SEQ ID NO:
- 35.
A method of generating a dominant negative allele of a first gene in a cell comprising deleting a second gene with a native promoter that is positioned in the opposite orientation relative to the first gene using a targeted editing technique, wherein the deletion results in the production of an antisense RNA transcript of the first gene under the control of the native promoter of the second gene, wherein the dominant negative allele is not exogenously introduced, and wherein the unmodified allele comprises a polynucleotide sequence having at least 95% identity or complementarity to a sequence selected from the group consisting of SEQ ID NOs:
- 1, 12, 27, 28, 29, 31, 32 and 33.
A modified plant cell comprising a non-transposon mediated genome deletion or inversion of a gene, or a portion thereof, at the endogenous locus of the gene, wherein the deletion or inversion results in the production of an antisense RNA transcript of the gene, or portion thereof, wherein the RNA transcript is under the control of a native promoter and was not exogenously introduced, wherein the gene is a GA20 oxidase gene, and wherein the GA20 oxidase gene is encoded by an mRNA that encodes a protein having at least 95% sequence identity to a sequence selected from the group consisting of SEQ ID NO:
- 30 and SEQ ID NO:
- 35.
A modified plant cell comprising a non-transposon mediated genome deletion or inversion of a gene, or a portion thereof, at the endogenous locus of the gene, wherein the deletion or inversion results in the production of an antisense RNA transcript of the gene, or portion thereof, wherein the RNA transcript is under the control of a native promoter and was not exogenously introduced, and wherein the unmodified allele comprises a polynucleotide sequence having at least 95% identity or complementarity to a sequence selected from the group consisting of SEQ ID NOs:
- 1, 12, 27, 28, 29, 31, 32 and 33.
Dependencies are inferred from the claim text.