Synthesis of double-stranded nucleic acids

Patent metadata

Field	Value
Publication number	US-10988795-B2
Application number	US-201515309237-A
Country	US
Kind code	B2
Filing date	May 15, 2015
Priority date	May 14, 2014
Publication date	Apr 27, 2021
Grant date	Apr 27, 2021

Abstract

The present invention relates to a method for the synthesis of double-stranded nucleic acids from a wide variety of samples and comprises the use of these nucleic acids for deep sequence analysis. Also, the present invention relates to specific reagents used in the method of the present invention. Further, the invention relates to kits comprising reagents for the method of the invention and use of said kits.

First claim

The invention claimed is:

1. A method for the synthesis of double stranded nucleic acid with a defined 3′ and 5′ terminal nucleotide sequence from a sample comprising single stranded nucleic acid comprising the steps of:
a) providing a sample comprising single stranded or double stranded nucleic acid,
b) performing a polynucleotide tailing reaction by adding at least 5 consecutive nucleotides to the 3′-terminus of the single stranded or double stranded nucleic acid,
c) hybridizing a priming oligonucleotide complementary to the added nucleotide sequence and synthesizing a cDNA or a cRNA with a template dependent DNA or RNA polymerase to generate a double stranded nucleic acid,
d) hybridizing a template switching oligonucleotide to said double stranded nucleic acid, and
e) extending the 3′ end of the cDNA or the cRNA strand to synthesize a double stranded nucleic acid, wherein one strand of the nucleic acid comprises the priming oligonucleotide, and a cDNA or a cRNA that is complementary to the single stranded nucleic acid and to the template switching oligonucleotide;
wherein said priming oligonucleotide comprises the following nucleotide sequence elements:
3′-W m -X-Y-Z1 o -Q t -Z2 s -5′,

wherein:
W at each instance is independently selected from dA, dG, dC, dT and dU;
X is selected from dA, dG, dC, dT, dU, rA, rG, rC, rT and rU;
Y is a polynucleotide of between 15 and 100 nucleotides length, wherein between 80% and 99% of the sequence is composed of dT or rT, wherein the other 1% to 20% of the sequence is composed of nucleotides or dinucleotides that are different from dT or rT, and are selected from dA, dG, dC, dT, dU, rA, rG, rC, rT, rU, AC, AG, AT, AU, CA, CG, CT, CU, GA, GC, GT, GU, TA, TC, TG, TU, AA, CC, GG, UU, UA, UC, UG, and UT, with the proviso that at least one of the nucleotides in the sequence is different from dT or rT, and with the proviso that X is different from the nucleotide or dinucleotide that constitutes the majority of Y;
Q is a sequence of consecutive degenerate (wobble) DNA bases;
Z1 is a polynucleotide of at least 5 nucleotides length of defined sequence, wherein the sequence is different from W m -X-Y;
Z2 is a polynucleotide of at least 5 nucleotides length of defined sequence, wherein the sequence is different from Wm-X-Y-Z1 o -Q t ;
m is an integer of 0 to 6, i.e. 0, 1, 2, 3, 4, 5 or 6;
o is 0 or 1;
s is 0 or 1; and
t is an integer of 0 to 6, i.e. 0, 1, 2, 3, 4, 5 or 6.

2. The method according to claim 1 , wherein the sample is a liquid or solid biopsy or derived thereof.

3. The method according to claim 1 , wherein the sample is obtained from fossils, remnants of extinct organisms, plants, fruits and animals, microbes, bacteria, or viruses.

4. The method according to claim 1 , wherein the single stranded nucleic acid is DNA.

5. The method according to claim 1 , wherein the consecutive nucleotides are identical, or consist of identical dinucleotides, trinucleotides, quadranucleotides, pentanucleotides or polynucleotides.

6. The method according to claim 5 , wherein the consecutive nucleotides are selected from the group consisting of identical ribonucleotides, deoxy-ribonucleotides or dideoxy-ribonucleotides of A, T, G, C, or U, or are selected from the group consisting of two or more ribo-dinucleotides or two or more deoxy-ribodinucleotides.

7. The method according to claim 1 , wherein the polynucleotide tailing reaction of step b) is performed with a mixture of two or more ribonucleotides or deoxyribonucleotides.

8. The method according to claim 6 , wherein the identical ribonucleotides, deoxy-ribonucleotides or dideoxy-ribonucleotides are added by an enzyme selected from the group consisting of poly(A)-polymerase, poly(U)-polymerase, poly(G)-polymerase, terminal transferase, a DNA ligase, and an RNA ligase, or wherein the two or more are added by an RNA ligase.

9. The method according to claim 1 , wherein Z1 and/or Z2 is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, and SEQ ID NO: 16.

10. The method according to claim 1 , wherein said template switching oligonucleotide is represented by the formula
5′-X p -Y-Q t -Z q -A r -3′

wherein
X is a chemical group selected from the group consisting of amino, biotin, glycerol, cholesterol, digoxigenin, fluoro residue or nucleotide derivatives including abasic nucleotides, dideoxy-ribonucleotides, 3′-deoxynucleotides, 2′-deoxyinosine, 2′-deoxyuridine;
Y is a known oligonucleotide sequence;
Q is a sequence of consecutive degenerate (wobble) DNA bases;
Z is a ribonucleotide selected from the group consisting of AMP, CMP, GMP, TMP and UMP,
A is a chemical group selected from the group consisting of amino, biotin, glycerol, cholesterol, digoxigenin, phosphate, fluoro residue or nucleotide derivatives including abasic nucleotides, dideoxy-ribonucleotides, 3′-deoxynucleotides, 2′-deoxyinosine, 2′-deoxyuridine;
t is an integer of 0 to 6, i.e. 0, 1, 2, 3, 4, 5 or 6;
p is an integer of 0 to 10, i.e. 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10;
q is an integer of at least 1; and
r is an integer of 0 to 10, i.e. 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10.

11. The method according to claim 10 , wherein Y of the template switching oligonucleotide is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, and SEQ ID NO: 16.

12. The method according to claim 1 , wherein said reverse transcriptase possesses DNA-polymerase activity and terminal transferase activity.

13. The method according to claim 1 , wherein said reverse transcriptase is able to switch to a template comprising a DNA/RNA and/or a DNA/DNA double stranded nucleic acid.

14. The method according to claim 1 , further comprising the step of immobilizing the synthesized double stranded nucleic acid on a surface.

15. The method according to claim 1 , further comprising the step f) of annealing to the double stranded nucleic acid synthesized in step e) at least one primer identical, complementary or capable of hybridizing to at least part of the priming oligonucleotide or the template switching oligonucleotide and carrying out a PCR amplification.

16. The method according to claim 15 , further comprising the step of immobilizing the product of the PCR amplification.

17. The method according to claim 15 , further comprising the step of determining at least part of the sequence of the single stranded nucleic acid.

18. A method for the synthesis of double stranded nucleic acid with a defined 3′ and 5′ terminal nucleotide sequence from a sample comprising single stranded nucleic acid comprising the steps of:
a) providing a sample comprising single stranded or double stranded nucleic acid,
b) performing a polynucleotide tailing reaction by adding at least 5 consecutive nucleotides to the 3′-terminus of the single stranded or double stranded nucleic acid,
c) hybridizing a priming oligonucleotide complementary to the added nucleotide sequence and synthesizing a cDNA or a cRNA with a template dependent DNA or RNA polymerase to generate a double stranded nucleic acid,
d) hybridizing a template switching oligonucleotide to said double stranded nucleic acid, and
e) extending the 3′ end of the cDNA or the cRNA strand to synthe

Assignees

• Univ Heidelberg Ruprecht Karls
• Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts
• Deutsches Krebsforsch

Inventors

• Turchinovich Andrey
• Surowy Harald
• Burwinkel Barbara

Classifications

• C12N15/1096

  cDNA Synthesis; Subtracted cDNA library construction, e.g. RT, RT-PCR · CPC title

• C12Q2531/113

  PCR · CPC title

• C12Q2525/161

  incorporating target specific and non-target specific sites · CPC title

• C12Q2525/173

  incorporating a polynucleotide run, e.g. polyAs, polyTs · CPC title

• C12Q1/6806 Primary

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title