Nucleic acid production and sequence analysis

• US 9,988,673 B2
• Filed: 03/17/2016
• Issued: 06/05/2018
• Est. Priority Date: 11/17/2011
• Status: Active Grant

• Current Assignee: Vilnius University
• Original Assignee: Vilnius University
• Inventors: Klimasauskas, Saulius, Stasevskij, Zdislav, Kriukiene, Edita
• Primary Examiner(s): Priest, Aaron A
• Application Number:
  US15/072,677
• Publication Number:
  US 20170016055A1
• Time in Patent Office: 810 Days
• Field of Search: None
• CPC Class Codes: C12P 19/34 Polynucleotides, e.g. nucleic acids, oligoribonucleotides
• CPC Class Codes: C12Q 1/6846 Common amplification features
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 1/6876 Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
• CPC Class Codes: C12Q 2521/125 Methyl transferase, i.e. methylase
• CPC Class Codes: C12Q 2525/117 incorporating modified base
• CPC Class Codes: C12Q 2525/155 incorporating/generating a new priming site
• CPC Class Codes: C12Q 2537/1373 Displacement by a nucleic acid

Abstract

A method for producing a nucleic acid molecule from a template nucleic acid sequence and a linking unit attached to a primer, which method comprises a step of contacting the template nucleic acid sequence with a nucleic acid polymerase under conditions which allow the nucleic acid polymerase to produce the nucleic acid molecule from the primer based on the template nucleic acid sequence, wherein the linking unit is attached to a target site in the template nucleic acid sequence with a covalent linkage.

Claims

1. A method for producing a nucleic acid molecule from a template nucleic acid sequence and a linking unit attached to a primer, which method comprises a step of contacting the template nucleic acid sequence with a nucleic acid polymerase under conditions which allow the nucleic acid polymerase to produce the nucleic acid molecule from the primer, wherein the linking unit is attached with a covalent linkage to a target site in the template nucleic acid sequence, wherein the linking unit comprises a primer binding region to which the primer is base paired and a linking region between the primer binding region and the covalent linkage, wherein the linking region does not base pair with the primer or with the nucleic acid molecule that is produced.

2. A method according to claim 1 comprising a step of forming the covalent linkage using a transferase enzyme.

3. A method according to claim 1 wherein the target site is within the template nucleic acid sequence and the linking unit is not attached with the covalent linkage to a terminal nucleotide of the template nucleic acid sequence.

4. A method according to claim 1 wherein the primer comprises no nucleotides that are complementary to the template nucleic acid at the start point of production of the nucleic acid molecule by the nucleic acid polymerase.

5. A method according to claim 1 wherein the primer is also covalently linked to the linking unit.

6. A method according to claim 1 further comprising a step of forming the covalent linkage between the template nucleic acid sequence and the linking unit by contacting the target site derivatized with a first reactive group, with a second reactive group attached to the linking unit, under conditions that allow the first reactive group to react with the second reactive group to form the covalent linkage.

7. A method according to claim 6 further comprising a step of derivatizing the target site with a first reactive group.

8. A method according to claim 7 wherein the step of derivatizing the target site comprises:

(i) contacting the template nucleic acid sequence with a compound and an enzyme, wherein the compound comprises the first reactive group, and wherein the enzyme is capable of transferring the first reactive group or a part of the compound comprising the first reactive group onto the target site;

or

(ii) contacting the template nucleic acid sequence with a compound, wherein the compound comprises the first reactive group, and the first reactive group or part of the compound comprising the first reactive group is transferred onto the target site through a reaction between the compound and the target site.

9. A method according to claim 8 wherein when the part of the compound comprising the first reactive group is transferred onto the target site, the method further comprises a step of uncovering the first reactive group so that the first reactive group is available for reaction with the second reactive group.

10. A method according to claim 1, further comprising a step of determining the sequence of the produced nucleic acid.

11. A method according to claim 1, further comprising a step of amplifying the produced nucleic acid.

12. A method according to claim 1 wherein the template nucleic acid sequence is DNA or RNA.

13. A method according to claim 1, wherein the target site comprises a nucleotide and the method further comprises, before the step of contacting the template nucleic acid sequence with a nucleic acid polymerase:

(a) derivatizing the nucleotide of the template nucleic acid sequence with a first reactive group by contacting the template nucleic acid sequence with;

(i) a target reactive compound comprising the first reactive group;

or (ii) a compound comprising a first reactive group and an enzyme, wherein the enzyme is capable of transferring the first reactive group, or a part of the compound comprising the first reactive group, onto the nucleotide;

(b) contacting the nucleic acid sequence with a second reactive group attached to the linking unit under conditions that allow the first reactive group to react with the second reactive group to form a covalent linkage, optionally wherein the linking unit is attached to the primer;

(c) optionally, where the primer is not attached to the linking unit in step (b), binding the primer to the linking unit;

and thereafter detecting the presence or absence of the produced nucleic acid molecule so as to determine the presence or availability of the target site.

14. A method according to claim 13 further comprising sequencing the produced nucleic acid molecule.

15. A method according to claim 13 further comprising a step of PCR amplification of the produced nucleic acid molecule.

16. A method according to claim 13, wherein when in step (a) the part of the compound comprising the first reactive group is transferred onto the nucleotide, the method further comprises a step prior to step (b) of uncovering the first reactive group.

17. A method according to claim 13 wherein the template nucleic acid sequence is an oligonucleotide.

18. A method according to claim 17 further comprising a step of forming the oligonucleotide by mechanical, enzymatic, or chemical digestion of DNA.

19. A method according to claim 18 wherein the step of mechanical digestion is DNA shearing.

20. A method according to claim 13 wherein the covalent linkage is selected from amide, thioureas, imidate, imine, thioether, disulfide, cyclic ester, hydrazone, oxime, thiaxolidine, 1,2,3-triazole, amide, cyclohexene, arylalkyne, biaryl, and diyne.

21. A method according to claim 13 wherein the first reactive group or the second reactive group is an amine, a thiol, a 1,2,-diol, a hydrazine, a hydroxylamine, a 1,2-aminothiol, an azide, a diene, a terminal alkyne, an arylhalide or a terminal silylalkyne, an N-hydroxysuccinimidyl ester, a thioester, an isothiocyanate, an imidoester, an aldehyde, a ketone, a maleimide, a haloacetamide, an aziridine, an arylboronic acid, an alkyne, a phosphane ester, a dienophile, or a terminal haloalkyne.

22. A method according to claim 13 wherein the first reactive group is a terminal alkyne, an amine, a hydroxylamine, a thiol, a maleimide, an alkyne, a hydrazide, an azide, or a carbodiimide.

23. A method according to claim 13 wherein the enzyme is a methyltransferase which is capable of using the compound as a co-factor.

24. A method according to claim 23 wherein the methyltransferase is a DNA methyltransferase or an RNA methyltransferase.

25. A method according to claim 24 wherein the DNA methyltransferase is M.SssI, M.MpeORF4940P, M.HhaI, M.HpaII, M.HsaDnmt1, M.HsaDnmt3A, M.HsaDnmt3B, M.MmuDnmt1, M.MmuDnmt3A, M.MmuDnmt3B, M.HaeIII, M.CviJI, M2.Eco31I, M.EcoRII, M.EcoDcm, M.MvaI, M.BstNI, M.TaqI, M.BseCI, M.Ecodam, T4Dam, M.RsrI or M.EcoRI.

26. A method according to claim 13, wherein the target site comprises an unmethylated cytosine, an unmodified adenine, a 5-hydroxymethylcytosine, or a modified cytosine.

27. A method according to claim 13 wherein the compound is an S-Adenosy-L-methionine analog.

28. A method according to claim 13 wherein the enzyme is a glucosyltransferase.

29. A method according to claim 13 wherein the primer and/or the linking unit further comprise an affinity binding group.

30. A method according to claim 29 further comprising a step of enriching the produced nucleic acid molecules using affinity binding.

32. A method according to claim 1 wherein the 3′

end of the primer is linked or non-covalently bound to the linking unit.

33. A method according to claim 13 wherein the primer comprises no nucleotides that are complementary to the template nucleic acid at the start point of production of the nucleic acid molecule by the nucleic acid polymerase.

34. A method according to claim 13 wherein step (a) is carried out ex vivo.

35. A method according to claim 13 wherein the template nucleic acid sequence is DNA or RNA.

36. A method according to claim 1, wherein the primer base paired to the nucleotide strand of the linking unit has a recessed 3′

end.

31. A template nucleic acid sequence attached to a linking unit and a primer, wherein the linking unit is attached to a target site in the template nucleic acid sequence with a covalent linkage, and wherein the 3′

end of the primer is attached to the linking unit.