Methods of controlling plant seed and organ size
This invention relates to the identification of a regulator protein (termed DA) which controls the size of plant seeds and organs in Arabidopsis and other plants. Manipulation of DA protein expression may useful, for example, in improving crop yield and increasing plant biomass.
1. A method of altering the phenotype of a higher plant comprising;
expressing a nucleic acid encoding a dominant-negative DA polypeptide within cells of said plant,
wherein the dominant-negative DA polypeptide comprises any one of SEQ ID NOs: 1 and 301 to 330 with
a mutation of R to K at a position corresponding to position 358 of SEQ ID NO: 1,
wherein the altered phenotype includes one or more traits selected from the group consisting of increased life-span, increased organ size and increased seed size relative to a control plants.
2. The method according to claim 1 further comprising reducing or abolishing expression of a Big Brother (BB) polypeptide within cells of said plant,
wherein the BB polypeptide comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 9 and has E3 ubiquitin ligase activity.
3. A method of producing a higher plant with an altered phenotype comprising:
incorporating a heterologous nucleic acid which encodes a dominant-negative DA polypeptide into a higher plant cell by means of transformation, and;
regenerating the higher plant from one or more transformed cells, wherein the higher plant comprises the heterologous nucleic acid which encodes a dominant-negative DA polypeptide, and
wherein the dominant-negative DA polypeptide comprises any one of SEQ ID NOs: 1 and 301 to 330 with a mutation of R to K at a position corresponding to position 358 of SEQ ID NO:1,
wherein the altered phenotype includes one or more traits selected from the group consisting of increased life-span, increased organ size and increased seed size relative to a control plants.
4. The method according to claim 3 further comprising incorporating a heterologous nucleic acid which expresses a suppressor nucleic acid which reduces expression of a BB polypeptide into said plant cell by means of transformation,
wherein the suppressor nucleic acid is a sense or anti-sense suppressor of BB polypeptide expression, and
wherein the BB polypeptide comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 9 and has E3 ubiquitin ligase activity.
5. The method according to claim 1 wherein the dominant-negative DA polypeptide comprises SEQ ID NO: 1 with a mutation of R to K at position 358.
6. The method according to claim 1 wherein the nucleic acid encoding the dominant negative DA polypeptide is operably linked to a heterologous promoter.
7. The method according to claim 6 wherein the promoter is a tissue-specific promoter.
8. The method according to claim 7 wherein the promoter is an inducible promoter.
9. The method according to claim 6 wherein the nucleic acid encoding the dominant negative DA polypeptide is comprised in one or more vectors.
10. The method according to claim 1 comprising sexually or asexually propagating or growing off-spring or descendants of the plant expressing the dominant-negative DA polypeptide.
11. The method according to claim 1 wherein the plant is an agricultural plant selected from the group consisting of Lithospermum erythrorhizon, Taxus spp, tobacco, cucurbits, carrot, vegetable brassica , melons, capsicums, grape vines, lettuce, strawberry, oilseed brassica , sugar beet, wheat, barley, maize, rice, soyabeans, peas, sorghum, sunflower, tomato, potato, pepper, chrysanthemum , carnation, linseed, hemp and rye.
12. A higher plant expressing a heterologous nucleic acid encoding a dominant-negative DA polypeptide within its cells,
wherein the dominant-negative DA polypeptide comprises any one of SEQ ID NOs:1 and 301 to 330 with
a mutation of R to K at a position corresponding to position 358 of SEQ ID NO: 1,
wherein the plant has an altered phenotype that includes one or more traits selected from the group consisting of increased life-span, increased organ size and increased seed size relative to a control plants.
13. The higher plant according to claim 12 which is produced by a method comprising:
incorporating said heterologous nucleic acid which encodes a dominant-negative DA polypeptide into a higher plant cell by means of transformation, and
regenerating the higher plant from one or more transformed cells.
14. A method of producing a dominant-negative DA polypeptide comprising:
providing a nucleic acid sequence encoding a plant DA polypeptide,
identifying an R residue in the encoded plant DA polypeptide at a position corresponding to position 358 of SEQ ID NO: 1, and
mutating the nucleic acid to substitute said R residue for a K residue in the encoded plant DA polypeptide,
the mutant nucleic acid sequence encoding a dominant negative DA polypeptide,
wherein the DA polypeptide comprises any one of SEQ ID NOs: 1 and 301 to 330.
15. A higher plant comprising an isolated DA1 or DAR which comprises any one of SEQ ID NOs: 1 and 301 to 330 with a mutation of R to K at a position corresponding to position 358 of SEQ ID NO: 1.
16. A method of altering the phenotype of a higher plant comprising:
expressing a nucleic acid encoding a dominant-negative DA polypeptide within cells of said plant,
wherein the dominant-negative DA polypeptide comprises any one of SEQ ID NOS: 1 and 301 to 330 with a mutation of R to K at a position corresponding to position 358 of SEQ ID NO: 1,
wherein the altered phenotype includes one or more traits selected from the group consisting of increased life-span, increased organ size and increased seed size relative to a control plant.