Method of characterizing a target ribonucleic acid (RNA) comprising forming a complementary polynucleotide which moves through a transmembrane pore

Patent metadata

Field	Value
Publication number	US-11111532-B2
Application number	US-201415028637-A
Country	US
Kind code	B2
Filing date	Oct 17, 2014
Priority date	Oct 18, 2013
Publication date	Sep 7, 2021
Grant date	Sep 7, 2021

Abstract

The invention relates to a new method of characterising a target ribonucleic acid (RNA) involving forming a complementary polynucleotide. The method uses a transmembrane pore.

First claim

The invention claimed is:

1. A method of characterising a target ribonucleic acid (RNA) comprising a poly A tail, the method comprising:
(a) forming a complementary polynucleotide from the target RNA by hybridising a primer to the poly A tail of the target RNA and using the primer to reverse transcribe the target RNA to form the complementary polynucleotide, wherein the primer comprises a leader sequence and/or a region to which a polynucleotide binding protein is capable of binding;
(b) contacting the complementary polynucleotide with a transmembrane pore such that the complementary polynucleotide moves through the pore; and
(c) taking one or more measurements as the complementary polynucleotide moves with respect to the pore wherein the measurements are indicative of one or more characteristics of the complementary polynucleotide and thereby characterising the target RNA,
wherein the method does not comprise polymerase chain reaction (PCR) or reverse transcription PCR (RT-PCR), and
wherein the complementary polynucleotide is contacted with the pore when the complementary polynucleotide is fully or partially hybridized to the targt RNA.

2. A method according to claim 1 , wherein the target RNA is eukaryotic.

3. A method according to claim 1 , wherein the primer is a polyT-VN primer, which comprises a polyT region and a VN anchor where V is dAMP, dCMP or dGMP and N is dAMP, dCMP, dGMP or dTMP.

4. A method according to claim 1 , wherein the complementary polynucleotide is coupled to the membrane.

5. A method according to claim 1 , wherein the one or more characteristics are selected from (i) the length of the target RNA, (ii) the identity of the target RNA, (iii) the sequence of the target RNA, and (iv) the amount of the target RNA.

6. A method according to claim 1 , wherein the one or more characteristics of the complementary polynucleotide are measured by electrical measurement and/or optical measurement.

7. A method according to claim 6 , wherein the electrical measurement is a current measurement, an impedance measurement, a tunnelling measurement or a field effect transistor (FET) measurement.

8. A method according to claim 1 , wherein step (b) comprises contacting the complementary polynucleotide with a polynucleotide binding protein such that the protein controls the movement of the complementary polynucleotide through the pore.

9. A method according to claim 8 , wherein the polynucleotide binding protein is a polymerase, exonuclease, helicase or a topoisomerase.

10. A method according to claim 1 , wherein the method comprises
(b) contacting the complementary polynucleotide with a transmembrane pore and a polynucleotide binding protein such that the protein controls the movement of the complementary polynucleotide through the pore; and
(c) measuring the current passing through the pore as the complementary polynucleotide moves with respect to the pore wherein the current is indicative of one or more characteristics of the complementary polynucleotide and thereby characterising the template RNA.

11. A method according to claim 1 , wherein the pore is a transmembrane protein pore or a solid state pore.

12. A method according to claim 11 , wherein the transmembrane protein pore is derived from a hemolysin, leukocidin, Mycobacterium smegmatis porin A (MspA), MspB, MspC, MspD, outer membrane porin F (OmpF), outer membrane porin G (OmpG), outer membrane phospholipase A, Neisseria autotransporter lipoprotein (NalP) or WZA.

13. A method according to claim 12 , wherein the transmembrane protein is:
(a) formed of eight identical subunits as shown in SEQ ID NO: 2 or (b) a variant thereof in which one or more of the eight subunits has at least 50% homology to SEQ ID NO: 2 based on amino acid identity over the entire sequence and retains pore activity; or
(c) formed of seven identical subunits as shown in SEQ ID NO: 4 or (d) a variant thereof in which one or more of the seven subunits has at least 50% homology to SEQ ID NO: 4 based on amino acid identity over the entire sequence and retains pore activity.

14. A method according to claim 1 , wherein the target RNA is messenger RNA (mRNA) or microRNA (miRNA).

15. A method according to claim 14 , wherein the mRNA or miRNA can be used to diagnose or prognose a disease or condition.

16. A method of determining whether or not a patient has or is at risk of developing a disease or condition associated with an altered amount and/or alternate splicing of messenger RNA (mRNA), comprising determining the amount and/or identity of the mRNA in a sample from the patient using a method according to claim 1 and thereby determining whether or not the patient has or is at risk of developing the disease or condition.

17. A method of characterising a target ribonucleic acid (RNA) comprising a polyA tail, comprising:
(a) forming a complementary polynucleotide from the target RNA by hybridising a primer to the polyA tail of the target RNA and using the primer to reverse transcribe the target RNA to form the complementary polynucleotide;
(b) contacting the complementary polynucleotide with a transmembrane pore such that the complementary polynucleotide moves through the pore; and
(c) taking one or more measurements as the complementary polynucleotide moves with respect to the pore wherein the measurements are indicative of one or more characteristics of the complementary polynucleotide and thereby characterising the target RNA;
wherein the complementary polynucleotide is contacted with the pore when the complementary polynucleotide is fully or partially hybridized to the target RNA.

18. A method according to claim 17 , wherein the method does not comprise polymerase chain reaction (PCR) or reverse transcription PCR (RT-PCR).

19. A method according to claim 17 , wherein the target RNA is eukaryotic.

20. A method according to claim 17 , wherein the primer is a polyT-VN primer, which comprises a polyT region and a VN anchor where V is dAMP, dCMP or dGMP and N is dAMP, dCMP, dGMP or dTMP.

21. A method according to claim 17 , wherein the complementary polynucleotide is coupled to the membrane.

22. A method according to claim 17 wherein the one or more characteristics are selected from (i) the length of the target RNA, (ii) the identity of the target RNA, (iii) the sequence of the target RNA, and (iv) the amount of the target RNA.

23. A method according to claim 17 , wherein the one or more characteristics of the complementary polynucleotide are measured by electrical measurement and/or optical measurement.

24. A method according to claim 23 , wherein the electrical measurement is a current measurement, an impedance measurement, a tunnelling measurement or a field effect transistor (FET) measurement.

25. A method according to claim 17 , wherein step (b) comprises contacting the complementary polynucleotide with a polynucleotide binding protein such that the protein controls the movement of the complementary polynucleotide through the pore.

26. A method according to claim 25 , wherein the polynucleotide binding protein is a polymerase, exonuclease, helicase or a topoisomerase.

27. A method according to claim 17 , wherein the method comprises
(b) contacting the complementary polynucleotide with a transmembrane pore and a polynucleotide binding protein such that the protein controls the movement of the complementary polynucleotide through the pore; an

Assignees

• Oxford Nanopore Tech Ltd

Inventors

• Brown Clive Gavin
• Turner Daniel John
• White James

Classifications

• C12Q1/6883

  for diseases caused by alterations of genetic material · CPC title

• C12Q2600/158

  Expression markers · CPC title

• C12Q1/6869 Primary

  Methods for sequencing · CPC title

• G01N27/4166

  measuring a particular property of an electrolyte · CPC title

• C12Q2600/118

  Prognosis of disease development · CPC title