Down-regulation of gene expression using artificial microRNAs
Isolated nucleic acid fragments comprising precursor miRNAs, and artificial miRNAs and their use in down-regulating gene expression are described.
1. An isolated nucleic acid fragment encoding an artificial microRNA (amiRNA) precursor, said fragment comprising a deoxyribonucleotide sequence wherein (i) nucleotides 249 to 269 of SEQ ID NO:16 are replaced by a first variable nucleotide subsequence ranging in size from 19 to 24 nucleotides depending upon a target sequence whose expression is to be reduced, (ii) nucleotides 316 to 336 of SEQ ID NO:16 are replaced by a second variable nucleotide subsequence ranging in size from 19 to 24 nucleotides, said second variable nucleotide subsequence being capable of hybridizing to the first variable subsequence, and (iii) the amiRNA precursor produced by said isolated nucleic acid fragment has the same stem structure as the precursor miRNa produced by endogenous SEQ ID NO:16.
2. A recombinant construct comprising the isolated nucleic acid fragment of claim 1 operably linked to at least one regulatory sequence.
3. A plant cell comprising the recombinant construct of claim 2 .
4. The plant cell of claim 3 wherein the plant cell is a monocot plant cell.
5. A method for reducing expression of a target sequence in a plant cell, said method comprising:
(a) transforming at least one plant cell with a nucleic acid construct encoding an artificial microRNA (amiRNA) precursor, said construct comprising a deoxynucleotide sequence wherein (i) nucleotides 249 to 269 of SEQ ID NO:16 are replaced by a first variable nucleotide subsequence ranging in size from 19 to 24 nucleotides depending upon the target sequence whose expression is to be reduced, (ii) nucleotides 316 to 336 of SEQ ID NO:16 are replaced by a second variable nucleotide subsequence ranging in size from 19 to 24 nucleotides, said second variable nucleotide subsequence being capable of hybridizing to the first variable subsequence, and (iii) the amiRNA precursor produced by said isolated nucleic acid fragment has the same stem structure as the precursor miRNa produced by endogenous SEQ ID NO:16; and
(b) selecting those transformed plant cell(s) whose level of expression of the target sequence is reduced when compared to the level of expression of the target sequence in a wild type plant cell.
6. The method of claim 5 wherein the plant cell is a monocot plant cell.
7. An artificial miRNA transcribed from the isolated nucleic acid fragment of claim 1 .