USE OF DOUBLE STRANDED RNA HAIRPIN DUPLEXES IN GENE SILENCING

BACKGROUND OF THE INVENTION

THIS INVENTION relates to gene silencing. More particularly the invention relates to use of double-stranded RNA hairpin duplexes in gene silencing.

Short hairpin RNAs (shRNAs) expressed from RNA Pol II and Pol III promoters can be used to silence target genes. shRNAs are expressed in the nucleus, and like microRNAs (miRNAs), are shuttled to the cytoplasm where the RNA interference (RNAi) machinery produces small interfering RNA (siRNAs). Typically, shRNAs include double stranded RNA (dsRNA) duplexes of up to 30 base pairs (bp) or nucleotides, which limits the number of functional siRNAs that can be generated from the hairpin precursor.

Long ds RNA hairpins (IhRNAs) and dsRNA duplexes can also be processed by the RNAi machinery into functional siRNAs. Typically, IhRNAs and dsRNA duplexes contain at least three DICER cleavage events and are therefore about 60 bp to 66 bp or longer.

Importantly, IhRNAs are capable of generating different siRNAs, and the number of different targeted siRNAs that are generated is directly proportional to the length of the dsRNA duplex (i.e. the IhRNA). Apart from targeting a greater genetic sequence, multiple siRNAs simultaneously target different sites, preventing the possible generation of mutant variants (i.e. for viral and cancer gene sequences) which may “escape” the targeted effects of siRNAs. Mutational escape is a phenomenon observed frequently for studies using shRNAs and siRNAs against viral targets and is not only limited to the target sequence but also to flanking sequences which affect local RNA secondary structures.

There are difficulties in cloning IdsRNA hairpins, however. Additionally, long dsRNA duplexes that are used in mammalian cells are known to activate the non-specific interferon response system in mammalian cells (e.g. PKR and Rnase L pathways). These difficulties in cloning and the immuno-stimulatory effect have limited the wide-spread application of long hairpins for gene silencing in mammalian and other cells. The major difficulties with long directly inverted repeats are the formation of cruciform junctions which cause genetic instability. This could lead to the rearrangement or splicing of the DNA constructs as the cell's recombination machinery can recognize cruciforms as Holliday junctions which are substrates for homologous recombination.

SUMMARY OF THE INVENTION

According to a first embodiment of the invention, there is provided a DNA polynucleotide comprising:

- a modified sequence of a target gene or a part thereof, wherein all or a substantial portion of any one type of nucleotide in the target gene sequence or the part thereof has been chemically modified to another type of nucleotide; and
- a complementary sequence of the unmodified target gene or the part thereof;
- wherein either one of the modified sequence or the complementary sequence is in a reverse orientation to the other sequence; and
- wherein the RNA sequence transcribed from the DNA polynucleotide forms a duplex between the modified sequence and the complementary sequence so that a long double stranded RNA (IdsRNA) duplex forms between the modified and complementary sequences with base pair mismatches where the nucleotides have been modified, the IdsRNA duplex being capable of inhibiting expression of the target gene.

The nucleotide modifications may be modifications of cytosine to thymine nucleotides, and the proportion of nucleotide modifications may be about one in every four to 10 nucleotides.

A further nucleotide sequence may be provided between the modified and complementary sequences, the further nucleotide sequence forming a hairpin loop in the RNA sequence between the modified and complementary sequences.

The target gene may be selected from the group consisting of metazoan, plant and viral genes. The metazoan genes may include mammalian, insect and nematode genes. In particular, the target gene may be a BC1 or AC1 gene from South African cassava mosaic virus (SACMV).

When the target gene is the SACMV BC1 gene, the modified sequence may comprise the nucleic acid sequence set forth in any one of SEQ ID NOs: 13, 16, 17 or 18, or a sequence which is at least 80% identical thereto; and the complementary fragment may comprise a nucleic acid sequence set forth in any one of SEC) ID NOs: 14, 15, 19 or 20, or a sequence which is at least 80% identical thereto. For example, the polynucleotide may include the sequence set forth in SEQ ID NO: 21.

When the target gene is the SACMV AC1 gene, the modified sequence may comprise the nucleic acid sequence set forth in any one of SEQ ID NOs: 33, 34, 35, 38, 39 or 40, or a sequence which is at least 80% identical thereto; and the complementary sequence may comprise a nucleic acid sequence set forth in any one of SEQ ID NOs: 36, 37, 41 or 42, or a sequence which is at least 80% identical thereto. For example, the polynucleotide may include the sequence set forth in SEQ ID NO: 53.

The modified and complementary sequences may each consist of more than 60 nucleotides.

The modified and complementary sequences may each consist of more than 80 nucleotides.

The modified and complementary sequences may each consist of more than 100 nucleotides.

Strand-specific amplification may be used to amplify the modified and complementary sequences, so as to ensure that the correct strand of the target gene is amplified.

According to a second embodiment of the invention, there is provided a RNA polynucleotide corresponding to the DNA polynucleotide described above.

The nucleotide modifications in the modified sequence may be cytosine to uracil modifications, and the base pair mismatches may be G:U mismatches.

The modified sequence may be set forth in any one of SEQ ID NOs: 22, 23, 24, 27, 28 or 29, or a sequence which is at least 80% identical thereto, and the complementary sequence may be set forth in any one of SEQ ID NOs: 25, 26, 30 or 31, or a sequence which is at least 80% identical thereto. For example, the RNA polynucleotide may comprise the sequence set forth in SEQ ID NO: 32.

The modified sequence may be set forth in any one of SEQ ID NOs: 43, 44, 45, 48, 49 or 50, or a sequence which is at least 80% identical thereto, and the complementary sequence may be set forth in any one of SEQ ID NOs: 46, 47, 51 or 52, or a sequence which is at least 80% identical thereto. For example, the RNA polynucleotide may comprise the sequence set forth in SEQ ID NO: 54.

According to a third embodiment of the invention, there is provided a long double stranded RNA (IdsRNA) duplex that inhibits the expression of a target gene, the IdsRNA duplex comprising:

- a modified sequence of the target gene or a part thereof, wherein all or a substantial portion of any one type of nucleotide in the target gene sequence or the part thereof has been chemically modified to another type of nucleotide; and
- a complementary sequence of the unmodified target gene or the part thereof;
- wherein the modified and complementary sequences form the IdsRNA duplex with base pair mismatches where the nucleotides have been modified.

The IdsRNA may be substantially as described above, or formed from a DNA or RNA polynucleotide described above.

According to a further embodiment of the invention, there is provided an expression cassette comprising the DNA polynucleotide described above.

The expression cassette may include either an RNA Pol II or an RNA Pol III promoter. The expression cassette may also include a termination signal which is an RNA Pol II or RNA Pol III termination signal.

According to a further embodiment of the invention, there is provided a nucleic acid vector which includes an expression cassette described above.

According to a further embodiment of the invention, there is provided a method of constructing a construct encoding a IdsRNA duplex, the method including:

- (i) PCR isolating a coding fragment of a target gene to obtain an untreated PCR product;
- (ii) treating at least a fraction of the untreated PCR product with a chemical mutagen, thereby causing chemical mutation of nucleotides of one type to nucleotides of another type so as to obtain a treated PCR product;
- (iii) conducting PCR on the treated PCR product to produce a nucleotide sequence with a proportion of mismatched nucleotides compared with the untreated PCR product;
- (iv) conducting PCR on the untreated PCR product; and
- (v) arranging the treated PCR product from (iii) encoding a sense strand and the untreated PCR product from (iv) encoding an anti-sense strand so that the treated PCR product and untreated PCR product are in a reverse orientation relative to each other.

There may be an intervening loop-encoding sequence between the treated PCR product and untreated PCR product. The intervening hairpin loop-encoding sequence may include at least one restriction site.

The PCR isolation may be by strand-specific PCR.

The method may further including the step of cloning the construct encoding the IdsRNA duplex.

Step (ii) may include subjecting the untreated PCR product to a bisulphite chemical mutagen, typically causing chemical mutation of unmethylated cytosines to thymines and producing a nucleotide sequence with cytosine to uracil mutations in step (iii).

According to a further embodiment of the invention, there is provided a method of silencing a target gene in a metazoan or plant subject, the method including the steps of:

- introducing an expression cassette including the DNA polynucleotide described above into the subject; and
- causing the expression cassette to express a RNA sequence or a IdsRNA duplex described above, thereby silencing said target gene.

The DNA or RNA polynucleotide or the IdsRNA described above may be used for silencing a target gene.

The DNA or RNA polynucleotide described above may also be used in a method of manufacturing a composition for use in a method of silencing a target gene in a metazoan or plant subject.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings in which:

FIG. 1 is a schematic illustration of the procedure for generation of long-hairpin RNAs (IhRNAs) that contain sense sequence changes to produce G:U mismatches in the dsRNA duplex. PCR primers are indicated as P1-P6 and the restriction enzyme digestion sites are shown as RE1-RE3.

FIG. 2 shows a workflow and methodology for the construction of a head-to-head cassette for the BC1 gene of SACMV. This methodology was applied for the construction of a head-to-head cassette for the AC1 gene of SACMV. Variations in restriction enzyme sites apply.

FIG. 3 shows the SACMV DNA A and SACMV DNA B genomes.

FIG. 4 shows the MSV genome.

FIG. 5A shows a 1.2% Agarose gel electrophoresis of BC1 and MSV AC1 PCR products. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 3: BC1 PCR Product. Lane 4: MSV AC1 PCR product.

FIG. 5B shows a 1.2% Agarose gel electrophoresis of SACMV AC1 PCR product. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 2: SACMV AC1 PCR Product.

FIG. 6A shows a 1.2% Agarose gel electrophoresis of sodium bisulfite-treated and untreated BC1 and MSV AC1 fragments. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 3: BC1 treated, 5 min, with modified BC1 primers. Lane 4: BC1 Treated 10 min, with modified BC1 primers. Lane 5: BC1 Treated 15 min, with modified BC1 primers. Lane 6: BC1 treated 2.5 hours, with modified BC1 primers. Lanes 7-8: H₂O controls. Lane 9: BC1 treated, 5 min, with unmodified BC1 primers. Lane 10: BC1 Treated 10 min, with unmodified BC1 primers. Lane 11: BC1 Treated 15 min, with unmodified BC1 primers. Lane 12: BC1 treated 2.5 hours, with unmodified BC1 primers. Lane 13: H₂O controls. Lane 17: BC1 untreated, with modified primers. Lane 18: H₂O control. Lane 20: BC1 untreated, with unmodified primers. Lane 21: H₂O control. Lane 24: MSV AC1 treated 2.5 hours, with modified primers. Lane 25: H₂O control. Lane 27: MSV AC1 treated 2.5 hours, with unmodified primers. Lane 28: H₂O control. Lane 30: MSV AC1 untreated, with modified primers. Lane 31: H₂O control. Lane 33: MSV AC1 untreated, with unmodified primers. Lane 34: H₂O control.

FIG. 6Bb shows a 1.2% Agarose gel electrophoresis of sodium bisulfite-treated and untreated SACMV AC1 fragments. Lane 1: AC1 treated 2.5 hours, with modified AC1 primers. Lane 2: AC1 untreated, with modified AC1 primers. Lane 3: AC1 treated 2.5 hours, with unmodified AC1 primers. Lane 4: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 5: H₂O control with modified AC1 primers. Lane 6: H₂O control with unmodified AC1 primers.

FIG. 7 shows a pTZ57R plasmid containing either BC1 or MSV AC1 inserts in the required orientations. This diagram was used as a basis for orientation screening.

FIG. 8A shows a 1.5% Agarose gel electrophoresis of BC1 untreated clones. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 3-8: Clones E26 to E21 Hinc II digestion to screen for orientation. Lanes 10-15: Clones E26 to E21 EcoRI and PstI digestion to screen for inserts.

FIG. 8B shows a 1.5% Agarose gel electrophoresis of an MSV AC1 untreated clone. Lane 1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 3: Clone G3 EcoRI and XhoI digestion to screen for orientation.

FIG. 8C shows a 1.5% Agarose gel electrophoresis of a pTZ-SACMV AC1 untreated clone. Lane 1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane2: Clone EcoRI and BgIII digestion to screen for orientation.

FIG. 9A shows a 1% Agarose gel electrophoresis of Clones B4 and E22 digestion. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lanes 3-4: Clone B4 (BC1 treated with sodium bisulfite) digestion with ScaI and BgIII. Lane 6-7: Clone E22 (BC1 untreated) digestion with ScaI and BamHI.

FIG. 9B shows a 1% Agarose gel electrophoresis of Clones F3 and G3 digestion. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lanes 3-4: Clone G3 (MSV AC1 untreated) digestion with ScaI and BamHI. Lane 6-7: Clone E22 (MSV AC1 treated with sodium bisulfite) digestion with ScaI and BgIII.

FIG. 9C shows a 1% Agarose gel electrophoresis of pTZ-SACMV AC1 clone. Lane1 & 3: O'Generuler 1 Kb Ladder Plus (Fermentas). Lane 2: AC1 treated clone digestion with ScaI and BgIII. Lane 4: AC1 untreated clone digestion with ScaI and BamHI.

FIG. 10A shows a 1% Agarose gel electrophoresis of BC1 hp clones. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lanes 3-7: BC1 hp clones 8-4 cut with XhoI and XbaI.

FIG. 10B shows a 1% Agarose gel electrophoresis of MSV AC1 hp clones. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lanes 3-7: MSV hp clones 1-6 cut with XbaI and SalI.

FIG. 10C shows a 1% Agarose gel electrophoresis of pTZ-SACMV AC1 hp clone. Lane1: O'Generuler 1 Kb Ladder Plus (Fermentas). Lanes 2 pTZ-SACMV AC1 hp clone cut with Pst1.

FIG. 11 shows a pTZ57R plasmid containing the double-insert in a head-to-head orientation.

FIG. 12A shows the BC1 ORF sequence and the MSV AC1 ORF sequence with targeted area underlined.

FIG. 12B shows the SACMV AC1 ORF sequence with targeted area underlined.

FIG. 13 shows a SACMV AC1 sequence with target area indicated.

FIG. 14 shows SACMV BC1 in reverse.

FIG. 15 shows MSV BC1 in reverse.

FIG. 16 shows SACMV BC1 target gene sequence.

FIG. 17 shows SACMV BC1 target gene region only.

FIG. 18 shows SACMV BC1 modified target gene region (i.e. a C to G modification)

FIG. 19 shows the complement of SACMV BC1 target gene sequence.

FIG. 20 shows complement of SACMV BC1 target gene region only.

FIG. 21 shows SACMV BC1 target gene sequence in reverse.

FIG. 22 shows SACMV BC1 target gene region in reverse.

FIG. 23 shows the modified target region of the SACMV BC1 gene in reverse.

FIG. 24 shows the reverse complement of the target gene sequence of the SACMV BC1 gene.

FIG. 25 shows the reverse complement of the target gene region of the SACMV BC1 gene.

FIG. 26 shows the SACMV BC1 hairpin sequence.

FIG. 27 shows the RNA sequence of the SACMV BC1 target gene.

FIG. 28 shows the RNA sequence of the SACMV BC1 target gene region.

FIG. 29 shows the RNA sequence of the modified SACMV BC1 target gene region.

FIG. 30 shows the RNA sequence of the complementary SACMV BC1 target gene.

FIG. 31 shows the RNA sequence of the complementary SACMV BC1 target region.

FIG. 32 shows the RNA sequence of the SACMV BC1 target gene in reverse.

FIG. 33 shows the RNA sequence of the SACMV BC1 target region in reverse.

FIG. 34 shows the RNA sequence of the modified SACMV BC1 target region in reverse.

FIG. 35 shows the RNA sequence of the reverse complement of the SACMV BC1 target gene.

FIG. 36 shows the RNA sequence of the reverse complement of the SACMV BC1 target gene region.

FIG. 37 shows the RNA sequence of the SACMV BC1 hairpin.

FIG. 38 shows SACMV AC1 target gene sequence.

FIG. 39 shows SACMV AC1 target gene region only.

FIG. 40 shows SACMV AC1 modified target gene region (i.e. a C to G modification)

FIG. 41 shows the complement of SACMV AC1 target gene sequence.

FIG. 42 shows complement of SACMV AC1 target gene region only.

FIG. 43 shows SACMV AC1 target gene sequence in reverse.

FIG. 44 shows SACMV AC1 target gene region in reverse.

FIG. 45 shows the modified target region of the SACMV AC1 gene in reverse.

FIG. 46 shows the reverse complement of the target gene sequence of the SACMV AC1 gene.

FIG. 47 shows the reverse complement of the target gene region of the SACMV AC1 gene.

FIG. 48 shows the RNA sequence of the SACMV AC1 target gene.

FIG. 49 shows the RNA sequence of the SACMV AC1 target gene region.

FIG. 50 shows the RNA sequence of the modified SACMV AC1 target gene region.

FIG. 51 shows the RNA sequence of the complementary SACMV AC1 target gene.

FIG. 52 shows the RNA sequence of the complementary SACMV AC1 target region.

FIG. 53 shows the RNA sequence of the SACMV AC1 target gene in reverse.

FIG. 54 shows the RNA sequence of the SACMV AC1 target region in reverse.

FIG. 55 shows the RNA sequence of the modified SACMV AC1 target region in reverse.

FIG. 56 shows the RNA sequence of the reverse complement of the SACMV AC1 target gene.

FIG. 57 shows the RNA sequence of the reverse complement of the SACMV AC1 target gene region.

FIG. 58 shows MSV AC1 target gene sequence.

FIG. 59 shows MSV AC1 target gene region only.

FIG. 60 shows MSV AC1 modified target gene region (i.e. a C to G modification)

FIG. 61 shows the complement of MSV AC1 target gene sequence.

FIG. 62 shows complement of MSV AC1 target gene region only.

FIG. 63 shows MSV AC1 target gene sequence in reverse.

FIG. 64 shows MSV AC1 target gene region in reverse.

FIG. 65 shows the modified target region of the MSV AC1 gene in reverse.

FIG. 66 shows the reverse complement of the target gene sequence of the MSV AC1 gene.

FIG. 67 shows the reverse complement of the target gene region of the MSV AC1 gene.

FIG. 68 shows the MSV AC1 hairpin sequence.

FIG. 69 shows the RNA sequence of the MSV AC1 target gene.

FIG. 70 shows the RNA sequence of the MSV AC1 target gene region.

FIG. 71 shows the RNA sequence of the modified MSV AC1 target gene region.

FIG. 72 shows the RNA sequence of the complementary MSV AC1 target gene.

FIG. 73 shows the RNA sequence of the complementary MSV AC1 target region.

FIG. 74 shows the RNA sequence of the MSV AC1 target gene in reverse.

FIG. 75 shows the RNA sequence of the MSV AC1 target region in reverse.

FIG. 76 shows the RNA sequence of the modified MSV AC1 target region in reverse.

FIG. 77 shows the RNA sequence of the reverse complement of the MSV AC1 target gene.

FIG. 78 shows the RNA sequence of the reverse complement of the MSV AC1 target gene region.

FIG. 79 shows the RNA sequence of the MSV AC1 hairpin.

FIG. 80 shows the SACMV AC1 hairpin sequence.

FIG. 81 shows the RNA sequence of the SACMV AC1 hairpin.

DETAILED DESCRIPTION OF THE INVENTION

Long double stranded RNA (IdsRNA) duplexes having mismatched base pairs are described herein.

Although IdsRNA duplexes are known, there currently exists a limitation to the ability to produce direct inverted repeats. Current technologies, such as intron-spliced hairpin constructs, are used as these are more stable than inverted repeats, but may be less effective. DNA cassettes for the expression of hairpin RNA of a length between 20 bp and 65 bp have included the use of synthetic oligonucleotides to make up the DNA cassette. However, this approach severely limits the size of the expressed long hairpin RNA that can be generated.

An alternative approach of generating IhRNAs by PCR of the desired target fragments and then cloning is hampered by the complementarity of the PCR amplified nucleotide sequences making up the stem of the RNA hairpin which result in cruciform structures that are difficult to clone. One method of preventing the formation of these structures is the use of long intron loops between the stem nucleotide sequences which are spliced out of the RNA transcript after transcription, leaving the dsRNA duplex.

The method of the present invention provides for the use of PCR amplified nucleotide sequences making up the stem of the RNA hairpin that contain mismatched bases, on average every 4 to 6 or 10 base pairs, although this will depend on the C:T content of the DNA and the duration and condition under which the DNA is chemically treated. The mismatched bases are generally introduced in the sense strand, ensuring that the formation of cruciform structures are less favorable, but leaving the anti-sense strand with sequence identity to the target sequence, thereby ensuring that RNAi inhibition of expression of the target gene can occur.

The IdsRNA duplexes of the present invention may be used in mammalian cells without stimulation of the non-specific interferon response.

The mismatched bases in the IdsRNA duplex are typically G:U mismatches, although any non-Watson-Crick pairing including wobble (i.e. where the mismatched base pairing is less stable than that of conventional A:U or G:C bonding), such as purine-purine or pyramidine-pyramidine base pairs may also be used. The mismatches result from the modification or substitution of some of the nucleotides in the IdsRNA duplex, such as by modifying a cytosine to uracil (GU base pairs are seemingly more stable than UG base pairs. The stability of UG base pairs is the same as the stability of AU/UA base pairs. GU base pairs are more stable than GC/CG basepairs). It is important to note that these pairings are all possible, but will just cause a greater distortion of the RNA hairpin structure due their varying stabilities. (Giese, M. R., Betschart, K., Dale, T., Riley, C. K., Rowan, C., Sprouse, K. J., Serra, M. J. 1998. Stability of RNA Hairpins Closed by Wobble Base Pairs. Biochemistry 37: 1094-1100). In the specific examples below, the mismatched bases in the IdsRNA duplex are produced by chemical mutation of the PCR amplified sense strand of the IdsRNA duplex with sodium bisulphite, although other methods of nucleic acid modification to generate mismatched bases known to those skilled in the art may also be used. Sodium bisulphite modifies unmethylated cytosines to thymines so that upon transcription, the mismatched nucleotide sequence includes cytosine to uracil mutations. It is also possible to completely synthesize a nucleotide fragment expressing the IdsRNA duplex such that there are mismatched bases in the sense strand.

C to T mutations were optimized for maximum stability and not G to As, using strand specific PCR primers.

The target gene may be selected from any organism. In addition, the IdsRNA duplexes may be used to silence genes from pathogens infecting these organisms, such as bacteria and viruses. For example, siRNAs have been used in the inhibition of genes from a number of pathogens, including human immunodeficiency virus (HIV), hepatitus virus C (HCV), hepatitus B virus (HBV) and influenza virus. In addition, siRNAs have been tested for inhibition of oncogenes in cancer treatment as well as against transposable elements, rogue elements and contagious genes.

Transgenic plants may be produced to express IdsRNA duplexes that inhibit expression of pathogen genes thereby generating a plant resistant to that pathogen, for example by targeting genes from cassava mosaic virus (e.g. BC1) or maize streak virus (e.g. AC1). The plant may also be capable of generating transgenic progeny that will be resistant to the pathogen. It is also possible to engineer tissue-specific expression, such as in the leaves of the plant, so that the dsRNA duplex is only expressed locally. Silencing constructs can also be expressed transiently.

Knock-out of genes in various organisms by IdsRNA may produce novel phenotypes that may be used commercially or for scientific research.

The target genes should be selected so that they do not have sequence identity to host genes that are not required to be silenced. Although the whole gene may be selected, it is also possible to use only a part of the target gene for generating dsRNA duplexes, such as a region of the target gene that is conserved between different strains or variants of the organism to be targeted, thereby limiting the effect of mutational escape from siRNA. It is not required that there be 100% sequence identity with the target sequence for the anti-sense strand of the dsRNA duplex to generate siRNAs that function. Typically, sequences with about 95%, about 90% or even about 80% sequence identity will be sufficient for the generated siRNAs to bind to and initiate silencing of the target sequence. The dsRNA duplex must be generated from an open reading frame, preferably an exon. In the specific examples below, the target region was selected on the basis of these preferred requirements.

The ability to generate multiple siRNAs from a single IdsRNA duplex provides for the possibility of simultaneously targeting different sites, preventing the possible generation of mutant variants (i.e. for viral and cancer gene sequences) which may “escape” the targeted effects of siRNAs.

The length of the nucleotide fragments making up the stem of the IdsRNA duplex can be from 60 nucleotides, and more preferably from 80 nucleotides or greater than 100 nucleotides, and may even be as large as it is possible to PCR amplify a nucleotide fragment. Currently, the typical maximum size is approximately 9 000 bp in length, although as the technology for PCR amplification improves this may increase in length. In addition, although it is currently prohibitively expensive to completely synthesize nucleotides that can be cloned to express IdsRNA duplexes, the cost of DNA synthesis is reducing and it is possible that this method may be used as an alternative to PCR amplification of the target gene fragments.

Although in the specific examples, there is a loop-encoding sequence between the nucleotide fragments making up the head-to-head construct of from 6 bp to 10 bp, the length of the loop sequence is not material to the transcription of or function of the IdsRNA duplex. As has been indicated above, the loop sequence may be over 1000 bp, such as in the case of intron, but it is also possible that no loop sequence is included, or that the loop sequence does not include an intron (e.g. it may include one or more restriction sites). Where a RNA transcript comprising complementary nucleotide fragments that can form a stem is expressed without a loop sequence included, a four-base loop would typically naturally form.

The specific examples provide for PCR amplification of a selected part of the target gene, followed by treatment of a portion of the PCR product generated with bisulphite to yield the modified PCR product with base pair mismatches compared with the unmodified product. These modified and unmodified fragments are then cloned into a standard commercially available vector, such that the fragments are arranged head-to-head or tail-to-tail with either the 3′ or 5′ ends, respectively, of the fragments oriented towards each other, with an intervening loop-encoding sequence. The cloned head-to-head construct can then be amplified by typical plasmid amplification. It is also possible to clone these products into alternative vectors known to those skilled in the art, such as cosmids or bacteriophage vectors.

It is possible to also isolate and mutate these fragments from restriction digest and not amplify.

The vector into which the head-to-head arrangement is cloned contains a promoter and a terminator sequence operably linked to the head-to-head arrangement in the specific examples, thereby forming an expression cassette for transcribing the IdsRNA duplex in the host cell.

The 35S CaMV promoter, which is a Pol II promoter, and is the most widely used promoter in plant transformation studies was used for the plants in this study. It has been shown that the 35S CaMV promoter works better in dicotyledonous plants than it does in monocotyledonous plants. An example of another Pol II promoter used in plant transformation is the rice ubiquitin promoter, which gives better expression in monocot plants (Wang, J., Oard, J. H., Rice ubiquitin promoters: deletion analysis and potential usefulness in plant transformation systems. Plant Cell Reports 22: 129-234). The terminator used in this study is the octopine synthase (OCS) terminator. Unfortunately, the actual terminator elements are poorly characterized and understood at this time, so the entire OCS gene is used to ensure proper termination and processing. Pol III promoters and terminators have also been used for the expression of artificial miRNAs in plants (Qu, J., Ye, J., Fang, R. 2007. Artificial MicroRNA-mediated virus resistance in plants. Journal of Virology 81: 6690-6699). Alternative promoters known to those skilled in the art for expression of RNA transcripts may also be used. The vector may also include further elements for selection, such as antibiotic resistance genes (e.g. kanamycin) or blue-white screening (e.g. β-galactosidase gene).

Once the expression cassettes encoding the IdsRNA duplex according to the invention have been generated, they may be introduced into the subject selected for silencing of the target gene of interest. As indicated above, the subject may be any organism or organism part in which the RNAi process functions to silence target gene expression.

The expression cassette may be introduced into the subject by varying methods of introduction known to a person skilled in the art, depending on the organism to be treated. For example, in plants the expression cassette may be introduced into the plant with the use of Agrobacterium transformed with a plasmid expressing the IdsRNA duplex, or plasmids expressing the IdsRNA duplex may be coated onto gold particles and bombarded into parts of the plant such as the leaves. These may then be propagated into new plants from leaf calluses, or expression of the IdsRNA may be allowed to occur in situ in the leaves.

In animal cells, the expression cassettes may be transformed into cells in tissue culture allowing expression of the IdsRNA transcript, or they may be introduced in vivo into animals or specific organs of the animal. There are many known methods for introduction of expression vectors into animal cells in tissue culture (e.g. CaCl₂transfection and liposome transfection) as well as into animals (e.g. plasmid-coated gold particle bombardment, air gun immunisation or injection) and these may all be used for introduction of the expression cassette expressing the IdsRNA duplex.

The expression cassette, once introduced into the host cell, then provides for transcription of the IdsRNA duplex which is processed by the cells' RNAi machinery into multiple siRNAs that target and silence the target gene. In the case of the specific examples, the siRNAs generated are targeted to the cassava mosaic virus BC1 gene, or to the maize streak virus AC1 gene inhibiting expression.

The present invention is further described by the following examples. Such examples, however, are not to be construed as limiting in any way either the spirit or scope of the invention.

EXAMPLES

The methodology herein describes the cloning of a specific region of the BC1 ORF of SACMV and a specific region of the AC1 ORF of MSV such that the identical fragments are cloned adjacent to each other in a head-to-head orientation (see FIG. 1). The cloning is facilitated by treating one of the fragments with sodium bisulfite prior to re-amplification and sub-cloning in a head-to-head orientation to express a IdsRNA duplex. The IdsRNA duplex is capable of being recognized by plant RNAi pathways to ensure the respective knockdown of SACMV (see FIG. 2) and MSV in infected plants.

Example 1

1.1 South African Cassava Mosaic Virus (SACMV) Targeting

PCR primers were designed to amplify a 222 bp region of the BC1 ORF (SEQ ID NO: 1) on the South African Cassava mosaic virus DNA B component (FIGS. 3 and 12). BC1 codes for a long distance movement protein that allows an SACMV infection to spread systemically through a plant.

1.2 Maize Streak Virus (MSV) Targeting

PCR primers were designed to amplify a 246 bp region of MSV replication associated protein A (MSV AC1) (SEQ ID NO: 2) (FIGS. 4 and 12). This protein is required for the replication of MSV.

Example 2

2.1 PCR Amplification of Target Sequences

For the amplification of BC1, 400 nmol of the PCR primers BC1 F (unmod) 5′ AAACATTCCACGGACATACG 3′ (SEQ ID NO: 3) and BC1 R (unmod) 5′ TGGTAGCCCAATCTGAGACCTT 3′ (SEQ ID NO: 4) were used with 15.4 ng of SACMV DNA-B template DNA. For the amplification of MSV AC1, 400 nmol of the PCR primers MSV AC1 F (Unmod) 5′ AGAGCTCCCCTTTGATTGG 3′ (SEQ ID NO: 5) and MSV AC1 R (Unmod) 5′ TCCATCCATTGGAGGTCAGAAAT 3′ (SEQ ID NO: 6) were used with 23.28 ng of MSV template DNA. The Triplemaster High Fidelity PCR system (Eppendorf) was used with standard Taq DNA polymerase according to manufacturers recommendations. Reactions were cycled in an Eppendorf thermal cycler at 95° C. for 2 minutes, followed by 30 cycles of 95° C. for 15 seconds, 52° C. for 15 seconds and 72° C. for 15 seconds. A final extension step of 72° C. for 20 minutes was done to allow for the addition of 3′ A overhangs to the PCR product. PCR products of the expected sizes were produced (FIG. 5). PCR products were purified using a High Pure PCR Product Purification kit (Roche).

2.2 Modification of PCR Products with Sodium Bisulfite

Depurination of cytosine residues in the PCR products was achieved by applying sodium bisulfite treatment in the EZ DNA Methylation-Gold kit (Zymo Research) to 120 ng BC1, and 360 ng MSV AC1 PCR products respectively. Reactions were set up according to the manufacturers recommendations. Samples were placed in a thermal cycler for 10 minutes at 98° C. to denature dsDNA, and were then methylated at 64° C. BC1 PCR products were depurinated at 4 different time points: 5 minutes, 10 minutes, 15 minutes, and 2.5 hours. MSV AC1 PCR products were methylated for 2.5 hours only, as was recommended by the manufacturer.

2.3 PCR Amplification of Sodium Bisulfite-Treated and Untreated DNA Templates

Sodium bisulfite treated BC1 fragments were amplified using original oligonucleotide primers BC1 F (unmod) and BC1 R (unmod), as well as a second set of modified primers: BC1 F (mod−XhoI+SpeI) 5′GATCCTCGAGACTAGTAAATATTCTACGGACATACG 3′ (SEQ ID NO: 7) and BC1 R (mod−BgIII) 5′ GATCAGATCTTAGTAGCCCAATCT AAGACCTTGT 3′ (SEQ ID NO: 8). These primers were designed to preferentially bind to the positive strand of the modified DNA template, as well as facilitating future directional cloning steps by introducing restriction endonuclease sites at both the 3′ and 5′ ends of the PCR product. Sodium Bisulfite treated MSV AC1 fragments were similarly amplified using the original primers MSV AC1 F (Unmod) and MSV AC1 R (Unmod), as well as a modified primer set: MSV AC1 F (Mod+SpeI) 5′ GATCACTAGTAGAGTTCTCC TTTGATTGG 3′ (SEQ ID NO: 9) and MSV AC1 R (Mod+BgIII+BclI) 5′ CTAGAGATCTTGATCATCCATCCATTAGAGATCAGAAAT 3′ (SEQ ID NO: 10). PCR amplification was done as described in 2.1.

It was observed that the modified primers as well as the original primers were able to efficiently amplify both the sodium bisulfite treated and untreated BC1 and MSV AC1 fragments (FIG. 6).

Example 3

3.1 Cloning of PCR Products

The treated PCR products were purified using a High Pure PCR Product Purification kit (Roche), and cloned into pTZ57R (Fermentas) using the InsT/A Clone PCR product cloning kit (Fermentas). Reactions were set up as recommended by the manufacturer; 39.96 ng (+/−0.54 pmol ends) of the BC1 PCR product (sodium bisulfite treated and untreated, respectively) was added to 165 ng linear pTZ57R (0.54 pmol ends), and 44.28 ng (+/−0.54 pmol ends) of the MSV AC1 PCR product (sodium bisulfite treated and untreated, respectively) was added to 165 ng linear pTZ57R (0.54 pmol ends). The ligation mixes were incubated at 22° C. for a minimum of 1 hour, after which they were used to transform competent DH5a cells. The competent cells were initially stored at −70° C., and were thawed on ice. Following this, 15 μl of the ligation mix was added to 50 μl of competent cells and incubated on ice for 20 minutes.

Cells were then heat shocked by placing them at 42° C. for 90 seconds, and then placing them on ice 2 minutes. The transformed cells were then spread plated onto LB agar plates containing 100 μg/ml Ampicillin, as well as X-GaI and IPTG for blue/white screening. Plates were incubated at 37° C. overnight, after which white colonies were selected and inoculated into 3 ml LB broth containing 100 μg/ml Ampicillin. After incubating this at 37° C. overnight, alkaline lysis DNA minipreps were done using a High Pure Plasmid Miniprep kit (Roche).

3.2 Screening of Clones

Restriction analysis was done on presumptive BC1 and MSV AC1 treated and untreated clones to screen for inserts and orientation. The BC1 (bisulfite treated) clones were screened using EcoRI and XhoI, whereas the untreated clones were screened by digestion with HincII. The MSV AC1 (bisulfite treated) clones were screened using EcoRI and BgIII, whereas the untreated clones were screened by digestion with EcoRI and XhoI.

Bisulfite treated clones that were presumptively in the right orientation were sequenced, and untreated clones were digested again to confirm orientation. FIG. 7 illustrates pTZ57R containing inserts in the right orientation.

3.2.1 BC1 and MSV AC1 Bisulfite Treated Clones—Sequencing

No correlation was found between incubation time and methylation of Cs, and the BC1 samples appeared to have been methylated to the maximum extent after 5 minutes. Clone A1 has an insert in the wrong orientation, and cannot be used. Clone D1 has guanine to adenine changes, which was caused by the PCR primers randomly amplifying the negative strand of the template DNA during the first round of PCR, thereby selecting the wrong strand. Methylation appears to be a random process, as a multiple alignment of clones A1, B4, C3 showed no distinct pattern of residues that had been changed.

Clone B4 was selected to be used in the construction of the BC1 hairpin, as it had a sufficient number of depurinations.

3.2.2 BC1 and MSV rep A Untreated Clones—Further Screening

TABLE 1

Sequencing results

Cytosine to
Guanine to

Clone

Thymine
Adenine
Correct

name
Description
changes*
changes
Orientation

A1
BC1 treated 5 min
42
0
N

B4
BC1 treated 10 min
39
0
Y

C3
BC1 treated 15 min
39
0
Y

D1
BC1 treated 2.5 h
0
7
Y

F3
MSV AC1 treated
58
0
Y

2.5 h

*There are a total of 70 cytosine residues in the BC1 fragment

Numerous BC1 and MSV AC1 clones were screened for orientation by digestion with restriction endonucleases as mentioned before.

Clones E21 to E26 (BC1 untreated) were found to all be in the right orientation, and have an insert of the right size. Similarly, clone G3 (MSV AC1 untreated) was in the right orientation (FIG. 8FIG. 3).

Example 4

4. Construction of Hairpins From Selected Clones.

In order to construct the hairpins from the selected clones. BC1 and MSV AC1 clones (sodium bisulfite treated), were digested with ScaI and BgIII. Similarly, the untreated clones were digested with ScaI and BamHI. Agarose gel electophoresis was used to separate the resulting fragments.

For clone B4, the 2042 bp fragment (top fragment) was excised from the gel and purified using the MinElute Gel Extraction kit (Qiagen). For clone E22, the 1312 bp fragment (lower fragment) was excised and purified. Similarly, for clone F3, the 2066 bp fragment (top fragment) was excised, and for clone G3 the 1337 bp fragment (lower fragment) was excised and purified.

Approximately 50 ng of each modified fragment was added with 50 ng of each unmodified fragment, respectively, to a ligation mix containing 1× ligation buffer, PEG 4000 and T4 DNA Polymerase (Fermentas). The mixture was incubated at 22° C. for a minimum of 1 hour, after which competent cells were transformed as described previously and plated. Presumptive BC1 hp clones were screened by restriction digestion with XhoI and XbaI. Presumptive MSV AC1 hp clones were screened by digestion with XbaI and SalI (FIG. 11).

The digestions showed that possible hairpins of the expected sizes are present. BC1 hp7 and MSV hp 3 were selected for further construction of the silencing cassette. Their fragments (FIG. 10) were excised from the gel and purified for later cloning into the vector pART 7.

Currently, experiments are underway to screen for siRNAs processed from the SACMV hairpin cassettes in transgenic Nicotiana benthamiana and cassava. Transgenic plants will be challenged with SACMV to determine knockdown of AC1 and BC1 and the effect of putative silencing on viral load. The applicant anticipates that plant lines expressing siRNAs derived from the mismatched IdsRNA hairpins will have reduced viral loads apon infection with SACMV. It is anticipated that the stability of the mismatched IdsRNAs will be comparable to that of long intron-spliced dsRNA in plants and will be more effective than perfectly matched inverted repeats. The stability of long intron-spliced inverted repeats is largely dependent upon the G:C content of the target gene, and therefore in the method described here, an increased stability can be achieved independently of the G:C content due to the nature of mutations described.

While the invention has been described in detail with respect to specific embodiments thereof, it will be appreciated by those skilled in the art that various alterations, modifications and other changes may be made to the invention without departing from the spirit and scope of the present invention. It is therefore intended that the claims cover or encompass all such modifications, alterations and/or changes.

USE OF DOUBLE STRANDED RNA HAIRPIN DUPLEXES IN GENE SILENCING

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

US Classifications

International Classifications

Abstract

Description

Claims

Priority Claims (1)

PCT Information