Mobile RNA acts as a signal to regulate plant growth and development
View Patent ↗The present invention relates to isolated nucleic acid molecules which encode a BEL transcription factor from potato ( Solanum tuberosum L.) and the amino acid sequences encoded by such nucleic acid molecules. The present invention also relates to a method of screening a biomolecule for its ability to assist in mediating long-distance movement of a mobile RNA in a plant.
1. A method of screening a biomolecule for its ability to assist in mediating long-distance movement of a mobile RNA in a plant, said method comprising:
providing a biomolecule;
providing a mobile RNA encoding a BEL transcription factor;
contacting the biomolecule with the mobile RNA under conditions effective for a biomolecule/mobile RNA complex to form; and
determining whether said contacting is effective in yielding a biomolecule/mobile RNA complex, thereby indicating that the biomolecule is able to assist in mediating long-distance movement of the mobile RNA in the plant.
2. The method according to claim 1 , wherein the biomolecule is a protein or polypeptide.
3. The method according to claim 1 , wherein the biomolecule is a ribonucleoprotein.
4. The method according to claim 1 , wherein BEL transcription factor is a protein or polypeptide having a molecular mass of about 56 kDa to about 76 kDa.
5. The method according to claim 1 , wherein said providing a mobile RNA comprises providing the 3′ untranslated region of the mobile RNA encoding a BEL transcription factor.
6. The method according to claim 1 , wherein the plant is selected from the group consisting of Gramineae, Liliaceae, Iridaceae, Orchidaceae, Salicaceae, Ranunculaceae, Magnoliaceae, Cruciferae, Rosaceae, Leguminosae, Malvaceae, Umbelliferae, Labiatae, Solanaceae, Cucurbitaceae, Compositae, and Rubiaceae.
7. The method according to claim 1 , wherein the plant is either a short-day-flowering plant or a long-day-flowering plant.
8. The method according to claim 7 , wherein the plant is a short-day-flowering plant selected from the group consisting of cotton, chrysanthemum, poinsettia, rice, orchid, soybean, strawberry, tobacco, and morning glory.
9. The method according to claim 7 , wherein the plant is a long-day-flowering plant selected from the group consisting of Arabidopsis , sugar beet, radish, spinach, winter barley, red clover, oat, tobacco, and wheat.
10. The method according to claim 1 , wherein said long-distance movement is through phloem tissue of the plant in a basipetal direction.
11. The method according to claim 1 , wherein said long-distance movement is through phloem tissue of the plant in an acropetal direction.
12. The method according to claim 1 , wherein the BEL transcription factor is encoded by a nucleic acid molecule having a nucleotide sequence comprising SEQ ID NO:1.
13. The method according to claim 1 , wherein the BEL transcription factor comprises a polypeptide having an amino acid sequence that is at least 85% similar to a homeodomain region, a SKY box, a BELL domain, and a VSLTLGL-box in SEQ ID NO:2 by basic BLAST using default parameters analysis.
14. The method according to claim 1 , wherein the BEL transcription factor is encoded by a nucleic acid molecule that hybridizes to the nucleotide sequence of SEQ ID NO:1 under stringent conditions characterized by a hybridization buffer comprising 5×SSC at a temperature of 55° C.
15. The method according to claim 1 , wherein the BEL transcription factor is a protein or polypeptide comprising the amino acid sequence of SEQ ID NO:2.
16. A method of screening a biomolecule for its ability to assist in mediating long-distance movement of a mobile RNA in a plant, said method comprising:
providing a biomolecule;
providing a mobile RNA encoding a KNOX transcription factor;
contacting the biomolecule with the mobile RNA under conditions effective for a biomolecule/mobile RNA complex to form; and
determining whether said contacting is effective in yielding a biomolecule/mobile RNA complex, thereby indicating that the biomolecule is able to assist in mediating long-distance movement of the mobile RNA in the plant.
17. The method according to claim 16 , wherein the KNOX transcription factor is from Solanum tuberosum.
18. The method according to claim 16 , wherein the mobile RNA has a nucleotide sequence of SEQ ID NO:16.
19. The method according to claim 16 , wherein the mobile RNA comprises a nucleic acid molecule that hybridizes to a nucleotide sequence of SEQ ID NO:16 under stringent conditions characterized by a hybridization buffer comprising 5×SSC at a temperature of 55° C.
20. The method according to claim 16 , wherein the mobile RNA encodes a protein or polypeptide having an amino acid sequence of SEQ ID NO:17.
21. The method according to claim 16 , wherein the plant is selected from the group consisting of Gramineae, Liliaceae, Iridaceae, Orchidaceae, Salicaceae, Ranunculaceae, Magnoliaceae, Cruciferae, Rosaceae, Leguminosae, Malvaceae, Umbelliferae, Labiatae, Solanaceae, Cucurbitaceae, Compositae, and Rubiaceae.
22. The method according to claim 16 , wherein the plant is either a short-day-flowering plant or a long-day-flowering plant.
23. The method according to claim 22 , wherein the plant is a short-day-flowering plant selected from the group consisting of cotton, chrysanthemum, poinsettia, rice, orchid, soybean, strawberry, tobacco, and morning glory.
24. The method according to claim 22 , wherein the plant is a long-day-flowering plant selected from the group consisting of Arabidopsis , sugar beet, radish, spinach, winter barley, red clover, oat, tobacco, and wheat.
25. The method according to claim 16 , wherein said long-distance movement is through phloem tissue of the plant in a basipetal direction.
26. The method according to claim 16 , wherein said long-distance movement is through phloem tissue of the plant in an acropetal direction.