Use of DNAzymes for analysis of an RNA sample
Provided herein is method comprising: contacting an initial RNA sample containing a population of different RNA molecules with a divalent cation and a set of DNAzymes that are designed to cleave multiple target RNAs in the initial sample, thereby producing a product RNA sample that comprises: a) uncleaved RNA molecules and b) cleaved RNA fragments that contain a 2′,3′-cyclic-phosphate and a 5′ hydroxyl as the result of DNAzyme cleavage.
1. A method comprising: contacting an initial RNA sample containing a population of different RNA molecules with a divalent cation and a set of DNAzymes that are designed to cleave multiple target RNAs in said initial sample, thereby producing a product RNA sample that comprises: a) uncleaved RNA molecules and b) cleaved RNA fragments that contain a 2′,3′-cyclic-phosphate and a 5′ hydroxyl as the result of DNAzyme cleavage; and
ligating a first adaptor onto the 3′ ends of at least some of said cleaved RNA fragments using a 2′,3′-cyclic phosphate-specific RNA ligase, thereby producing a ligated sample comprising ligation products.
2. The method of claim 1 , wherein said DNAzymes are 10-23 DNAzymes.
3. The method of claim 1 , wherein contacting is done by cycling through denaturation and renaturation temperatures to maximize cleavage by said DNAzyme.
4. The method of claim 1 , wherein said set of DNAzymes comprises at least 100 different DNAzymes that specifically target different RNAs.
5. The method of claim 1 , wherein said first adaptor comprises a 5′-phosphate or 5′-hydroxyl and said ligase is a eukaryotic tRNA ligase.
6. The method of claim 1 , wherein said first adaptor comprises a 5′-hydroxyl and said ligase is an RtcB ligase.
7. The method of claim 1 , wherein said first adaptor is labeled, and the method produces a labeled RNA sample.
8. The method of claim 7 , wherein said method further comprises: a) hybridizing said labeled RNA sample to an array; b) reading said array to provide results, and c) analyzing said results to obtain information on said initial sample.
9. The method of claim 1 , wherein the first adaptor comprises an RNA polymerase promoter and said method comprises: a) making double stranded cDNA from said product RNA sample using a primer that hybridizes with said first adaptor and a reverse transcriptase, and b) transcribing the cDNA using an RNA polymerase in the presence of labeled a rNTP, thereby making labeled RNA.
10. The method of claim 1 , wherein said method comprises: a) making cDNA from said product RNA sample using a primer that hybridizes with said first adaptor and a reverse transcriptase; b) adding a second adaptor to said cDNA at the opposite end to said first adaptor; c) amplifying said cDNA using primers that bind to said first adaptor and second adaptors.
11. The method of claim 10 , wherein further comprising sequencing said cDNA.
12. The method of claim 1 , wherein said first adaptor contains an affinity tag, and said method further comprises purifying said ligation products from other molecules in said ligated sample using said affinity tag.
13. A method comprising:
contacting an initial RNA sample comprising a population of RNA molecules that have a 3′ adaptor and a 5′ adaptor with a divalent cation and a set of DNAzymes that are designed to cleave multiple target RNAs in said initial sample, thereby producing a product RNA sample that comprises: a) uncleaved RNA molecules and b) cleaved RNA fragments that contain a 2′,3′-cyclic-phosphate and a 5′ hydroxyl as the result of DNAzyme cleavage.
14. The method of claim 13 , wherein said method comprises, after said contacting, making cDNA using a primer that hybridizes with said 3′ adaptor.
15. The method of any of claim 13 , further comprising amplifying cDNA copied from said uncleaved RNA molecules using primers that are complementary to the 3′ and 5′ adaptors.
16. The method of claim 15 , wherein said method further comprises sequencing said cDNA.
17. A method comprising: contacting an initial RNA sample containing a population of different RNA molecules with a divalent cation and a set of DNAzymes that are designed to cleave multiple target RNAs in said initial sample to produce an RNA sample that comprises: a) uncleaved RNA molecules and b) cleaved RNA fragments that contain a 2′,3′-cyclic-phosphate and a 5′ hydroxyl as the result of DNAzyme cleavage, wherein the set of DNAzymes comprises a first DNAzyme and a second DNAzyme that both the cleave the same RNA molecule to produce an RNA product that has a defined sequence of nucleotides at its ends; and ligating the ends of said RNA product to an adaptor to produce a circular product molecule.