Two-color real-time/end-point quantitation of microRNAs (miRNAs)
View Patent ↗The present invention is directed to methods, reagents, kits, and compositions for detecting target polynucleotide sequences, especially small target polynucleotides such as miRNAs, between two samples. A pair of linker probes can be employed in two different reactions to query a particular species of target polynucleotide. A pair of detector probes, a single forward primer specific for the target polynucleotide, and a reverse primer can be employed in an amplification reaction to query the difference in expression level of the target polynucleotide between the two samples. In some embodiments a plurality of small miRNAs are queried with a plurality of linker probes. The plurality of queried miRNAs can then be decoded in a plurality of amplification reactions.
1. A method for quantifying a small target polynucleotide in each of two samples comprising;
providing a first reaction mixture comprising a small target polynucleotide from a first sample, and a first linker probe, wherein the first linker probe comprises a 3′ target-specific portion, a stem, and a loop, wherein the 3′ target-specific portion base pairs with the 3′ end of the target polynucleotide;
providing a second reaction mixture comprising a small target polynucleotide from a second sample, and a second linker probe, wherein the second linker probe comprises a 3′ target-specific portion, a stem, and a loop, wherein the 3′ target-specific portion base pairs with the 3′ end of the target polynucleotide, wherein the small target polynucleotide in the first reaction mixture is the same species as the small target polynucleotide in the second reaction mixture;
hybridizing the first linker probe to the small target polynucleotide in the first reaction mixture to form a first target-linker probe complex, and extending the first linker probe to form a first extension product;
hybridizing the second linker probe to the small target polynucleotide in the second reaction mixture to form a second target-linker probe complex, and extending the second linker probe to form a second extension product;
combining the first extension reaction product and the second extension reaction product to form a pooled reaction mixture;
PCR amplifying the first extension reaction product and the second extension reaction product in the presence of a first detector probe and a second detector probe to form an amplified first extension reaction product and an amplified second extension reaction product, wherein the first detector probe corresponds to the amplified first extension reaction product and the second detector probe corresponds to the second amplified second extension reaction product, wherein the stem of the first linker probe comprises a first sample identifying portion and the stem of the second linker probe comprises a second sample identifying portion, and the first detector probe hybridizes to the corresponding sample identifying portion of the amplified first extension reaction product and the second detector probe hybridizes to the corresponding sample identifying portion of the amplified second extension reaction product during the amplification reaction, wherein at least one of the first detector probe and the second detector probe further hybridizes to sequence corresponding to the small target polynucleotide during the amplification reaction; and,
detecting the quantity of the small target polynucleotide in the two samples by comparing the first detector probe and the second detector probe.
2. The method according to claim 1 wherein the small target polynucleotide is a micro RNA.
3. The method according to claim 1 wherein at least one of the detector probes comprise peptide nucleic acid (PNA).
4. The method according to claim 1 wherein at least one of the detector probes is a 5′-nuclease cleavable probe.
5. The method according to claim 1 wherein each strand of the self-complementary stem of the first linker probe and/or second linker probe comprises 12-16 nucleotides.
6. The method according to claim 1 wherein the target specific portion of the first linker probe, the second linker probe, or both, comprises 6-8 nucleotides.
7. The method according to claim 1 wherein the loop further comprises a universal reverse primer portion.
8. The method according to claim 1 wherein the loop comprises 14-18 nucleotides.
9. The method according to claim 1 ,
wherein the first reaction mixture comprises a plurality of different linker probes corresponding to a plurality of different small target polynucleotide species,
wherein the second extension reaction mixture comprises a plurality of different linker probes corresponding to a plurality of different small target polynucleotide species,
wherein the pooled extension reaction products of the pooled reaction mixture are subsequently subdivided into a plurality of amplification reactions,
wherein each amplification reaction comprises a primer pair, a first detector probe corresponding to the first sample, and a second detector probe corresponding to the second sample,
wherein a small target polynucleotide is detected in each amplification reaction.
10. The method according to claim 9 wherein at least one primer pair comprises a forward primer corresponding to a small target polynucleotide, and a universal reverse primer corresponding to a universal reverse primer portion of a loop of the linker probe.
11. The method according to claim 1 wherein the detecting comprises an end-point analysis.
12. The method according to claim 1 wherein the detecting comprises a real-time analysis.
13. The method according to claim 12 wherein the real-time analysis is performed on a real-time thermal-cycler.
14. The method of claim 1 , wherein the small target polynucleotide is 25 or fewer nucleotides in length.