Gene silencing
The invention provides methods and compositions useful in target sequence suppression and target sequence validation. The invention provides polynucleotide constructs useful for gene silencing, as well as cells, plants and seeds comprising the polynucleotides. The invention also provides a method for using microRNA to silence a target sequence.
1. A method of inhibiting expression of a target sequence in a plant cell comprising:
(a) introducing into the plant cell a nucleic acid construct comprising a promoter operably linked to a polynucleotide encoding a modified SEQ ID NO:1, wherein the polynucleotide comprises in the following order:
(i) a first heterologous sequence,
(ii) the modified SEQ ID NO:1, wherein SEQ ID NO:1 has been modified only in a backside region or a miRNA template region, or both, as follows:
(1) the backside region consists of a first oligonucleotide of 21 contiguous nucleotides, wherein the first oligonucleotide is either fully complementary to a second oligonucleotide of 21 contiguous nucleotides or has 1, 2, 3, 4, or 5 mismatches, and
(2) the miRNA template region consists of the second oligonucleotide of 21 contiguous nucleotides, wherein the second oligonucleotide encodes a miRNA, and wherein the second oligonucleotide is either fully complementary to the target sequence or has 1, 2, 3, 4, or 5 mismatches, and
(iii) a second heterologous sequence,
wherein at least one of the first and the second oligonucleotide is heterologous to SEQ ID NO:1, and further wherein the polynucleotide encodes an RNA precursor capable of forming a hairpin, and
(b) expressing the nucleic acid construct for a time sufficient to produce the miRNA, wherein the miRNA inhibits expression of the target sequence.
2. The method of claim 1 , wherein target sequence expression is inhibited by at least 10%.
3. The method of claim 1 , wherein inhibition of the target sequence generates a loss-of-function phenotype.
4. The method of claim 1 , wherein the promoter is a pathogen-inducible promoter and inhibition of the target sequence confers resistance to a pathogen.
5. A nucleic acid construct comprising a promoter operably linked to an isolated polynucleotide encoding a modified SEQ ID NO:1, wherein the polynucleotide comprises in the following order:
(i) a first heterologous sequence,
(ii) the modified SEQ ID NO:1, wherein SEQ ID NO:1 has been modified only in a backside region or a miRNA template region, or both, as follows:
(1) the backside region consists of a first oligonucleotide of 21 contiguous nucleotides, wherein the first oligonucleotide is either fully complementary to a second oligonucleotide of 21 contiguous nucleotides or has 1, 2, 3, 4, or 5 mismatches, and
(2) the miRNA template region consists of the second oligonucleotide of 21 contiguous nucleotides, wherein the second oligonucleotide encodes a miRNA, and the second oligonucleotide is either fully complementary to a target sequence or has 1, 2, 3, 4, or 5 mismatches, and
(iii) a second heterologous sequence,
wherein at least one of the first and the second oligonucleotides is heterologous to SEQ ID NO:1, and further wherein the polynucleotide encodes an RNA precursor capable of forming a hairpin.
6. A cell comprising the nucleic acid construct of claim 5 .
7. The cell of claim 6 , wherein the cell is a plant cell.
8. A transgenic plant comprising the nucleic acid construct of claim 5 .
9. A transgenic seed comprising the nucleic acid construct of claim 5 .
10. The nucleic acid construct of claim 5 , wherein the promoter is a pathogen-inducible promoter.
11. The nucleic acid construct of claim 5 , wherein the nucleic acid construct suppresses expression of a target sequence.
12. The method of any one of claim 2 , 3 , or 4 , the method further comprising producing a transformed plant, wherein the plant comprises the nucleic acid construct which encodes the miRNA.