Methods to detect ribonucleotides in deoxyribonucleic acid
Genomic DNA contains embedded ribonucleotides (rNMPs) that are incorporated during DNA replication and repair, or formed during DNA damage. The modifications have been linked to genome instability and disease, but no method currently exists to profile their locations genome-wide. rNMP incorporation has been extensively studied in recent years; however, locating sites of rNMP incorporation in genomic DNA has not yet been possible. Disclosed herein is a unique method for mapping rNMPs in genomic DNA that exploits the unique ligation mechanism of Arabidopsis thaliana tRNA ligase (AtRNL), normally involved in tRNA maturation. As disclosed herein AtRNL captures 2′,3′-cyclic phosphate or 2′-phosphate termini of DNA derived from alkaline cleavage of a DNA oligonucleotide (oligo) at an embedded rNMP, ligating the 2′-phosphate end to the 5′-phosphate terminus of the same DNA molecule and producing a ssDNA circle containing an embedded rNMP.
1. A method of detecting a ribonucleotide in a molecule of deoxyribonucleic acid (DNA), the method comprising:
ligating a first adaptor to a fragment of genomic DNA, wherein the adaptor comprises: a first primer-binding sequence;
a first annealing sequence, wherein the first annealing sequence is coupled to the first primer-binding sequence;
and a unique molecular identifier (UMI) sequence, wherein the UMI sequence is coupled to the first primer-binding sequence;
cleaving the fragment of genomic DNA via an alkali treatment;
ligating the cleaved fragment of genomic DNA using an Arabidopsis thaliana tRNA ligase (AtRNL) to produce a circular single stranded DNA fragment;
amplifying the circular single stranded DNA fragment using polymerase chain reaction (PCR) to produce a PCR product using a first primer that is capable of specifically binding the first primer-binding sequence and a second primer that is capable of specifically binding a second primer-binding sequence; and sequencing the PCR product.
2. The method of claim 1 , further comprising the step of removing a 2′-phosphate from the circular single stranded DNA fragment prior to amplifying the circular single stranded DNA fragment.
3. The method of claim 1 , wherein the AtRNL has an amino acid sequence that is 90-100% identical to SEQ ID NO: 1 or SEQ ID NO: 2.
4. The method of claim 3 , wherein the AtRNL has blunt-end ligase activity.
5. The method of claim 1 , wherein the molecule of DNA is obtained from a cell.
6. The method of claim 5 , wherein the cell is a eukaryotic cell or a prokaryotic cell.
7. The method of claim 6 , further comprising ligating a second adaptor to the cleaved fragment of genomic DNA on the end opposite of where the first adaptor is ligated, wherein the second adaptor comprises a second annealing sequence and wherein the second annealing sequence is identical to the first annealing sequence.
8. The method of claim 1 , wherein the fragment of genomic DNA has blunt ends.
9. The method of claim 1 , further comprising the step of fragmenting genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
10. The method of claim 1 , further comprising the step of dA-tailing the fragment of genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
11. The method of claim 1 , further comprising the step of removing a linear single stranded DNA after the step of ligating the cleaved fragment of genomic DNA.
12. The method of claim 1 , wherein the adaptor further comprises a second primer-binding sequence.
13. A method of detecting a ribonucleotide in a molecule of deoxyribonucleic acid (DNA), the method comprising:
ligating an adaptor to a fragment of genomic DNA, wherein the adaptor comprises:
a first primer-binding sequence;
a second primer-binding sequence, wherein the second primer-binding sequence is coupled to the first primer-binding sequence;
a first annealing sequence, wherein the first annealing sequence is coupled to the first primer-binding sequence; and
a unique molecular identifier (UMI) sequence, wherein the UMI sequence is coupled to the first primer-binding sequence;
cleaving the fragment of genomic DNA via an alkali treatment;
ligating the cleaved fragment of genomic DNA using an Arabidopsis thaliana tRNA ligase (AtRNL) to produce a circular single stranded DNA fragment;
amplifying the circular single stranded DNA fragment using polymerase chain reaction (PCR) to produce a PCR product, using a first primer that is capable of specifically binding the first primer-binding sequence and a second primer that is capable of specifically binding the second primer-binding sequence; and sequencing the PCR product.
14. The method of claim 13 , further comprising the step of removing a 2′-phosphate from the circular single stranded DNA fragment prior to amplifying the circular single stranded DNA fragment.
15. The method of claim 13 , wherein the fragment of genomic DNA has blunt ends.
16. The method of claim 13 , further comprising the step of fragmenting genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
17. The method of claim 13 , further comprising the step of dA-tailing the fragment of genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
18. The method of claim 13 , further comprising the step of removing a linear single stranded DNA after the step of ligating the cleaved fragment of genomic DNA.
19. The method of claim 13 , further comprising ligating a second adaptor to the cleaved fragment of genomic DNA on the end opposite of where the first adaptor is ligated, wherein the second adaptor comprises a second annealing sequence and wherein the second annealing sequence is identical to the first annealing sequence.
20. A method of detecting a ribonucleotide in a molecule of deoxyribonucleic acid (DNA), the method comprising:
ligating an adaptor to a fragment of genomic DNA, wherein the adaptor comprises: a first primer-binding sequence;
a first annealing sequence, wherein the first annealing sequence is coupled to the first primer-binding sequence; and a unique molecular identifier (UMI) sequence, wherein the UMI sequence is coupled to the first primer-binding sequence;
cleaving the fragment of genomic DNA via an alkali treatment;
ligating the cleaved fragment of genomic DNA using a ligase capable of coupling a 2′,3′-cyclic phosphate to a 5′-phosphate to produce a circular single stranded DNA fragment;
amplifying the circular single stranded DNA fragment using polymerase chain reaction (PCR) to produce a PCR product; and
sequencing the PCR product using a first primer that is capable of specifically binding the first primer-binding sequence.
21. The method of claim 20 , wherein the ligase is an Arabidopsis thaliana tRNA ligase (AtRNL).
22. The method of claim 21 , wherein the AtRNL has an amino acid sequence that is 90-100% identical to SEQ ID NO: 1 or SEQ ID NO: 2.
23. The method of claim 20 , wherein the ligase is an RtcB ligase.
24. The method of claim 23 , wherein the RtcB ligase has an amino acid sequence that is 90-100% identical to SEQ ID NO: 3.
25. The method of claim 21 , further comprising the step of removing a 2′-phosphate from the circular single stranded DNA fragment prior to amplifying the circular single stranded DNA fragment.
26. The method of claim 21 , wherein the fragment of genomic DNA has blunt ends.
27. The method of claim 21 , further comprising the step of fragmenting genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
28. The method of claim 21 , further comprising the step of dA-tailing the fragment of genomic DNA prior to the step of ligating the adaptor to the fragment of genomic DNA.
29. The method of claim 21 , further comprising the step of removing a linear single stranded DNA after the step of ligating the cleaved fragment of genomic DNA.
30. The method of claim 21 , wherein the adaptor further comprises a second primer-binding sequence.
31. The method of claim 30 , further comprising the step of sequencing the PCR product using a second primer that is capable of specifically binding the second primer-binding sequence, wherein the step of sequencing the PCR product using the second primer is performed simultaneously or sequentially with the step of sequencing the PCR product using the first primer that is capable of specifically binding the first primer-binding sequence.
32. The method of claim 31 , wherein the ligase has blunt-end ligase activity.
33. The method of claim 31 , wherein the molecule of DNA is obtained from a cell.
34. The method of claim 33 , wherein the cell is a eukaryotic cell or a prokaryotic cell.
35. The method of claim 20 , further comprising ligating a second adaptor to the cleaved fragment of genomic DNA on the end opposite of where the first adaptor is ligated, wherein the second adaptor comprises a second annealing sequence and wherein the second annealing sequence is identical to the first annealing sequence.