Method of monitoring RNase L activity

Patent metadata

Field	Value
Publication number	US-11859234-B2
Application number	US-201716099237-A
Country	US
Kind code	B2
Filing date	May 5, 2017
Priority date	May 6, 2016
Publication date	Jan 2, 2024
Grant date	Jan 2, 2024

Abstract

The present disclosure relates, in general, to a method for generating chimeric DNA derived from RNase L cleavage products in a sample, and detection of such RNase L cleavage products for diagnosis and treatment of inflammation and infection in a subject.

First claim

What is claimed:

1. A method for detecting an RNase L cleavage product comprising,
a) isolating total RNA or small RNAs from a sample;
b) ligating a ligation adapter polynucleotide to the RNA from the sample cleaved by RNase L, wherein the ligation adapter polynucleotide specifically ligates to RNA that has been cleaved by RNaseL, wherein the ligation adapter polynucleotide has at its 5′ end at least 1 nucleotide that is identical to a 3′ end of a first primer;
c) generating cDNA by reverse-transcription of the RNA-ligation adapter polynucleotide ligation product using a reverse transcription primer that is complementary to at least a portion of the ligated ligation adapter polynucleotide;
d) contacting the cDNA with the first primer, having at its 3′ end at least 1 nucleotide identical to the ligation adapter polynucleotide 5′ end and further comprising nucleotides identical to at least a portion of the sequence of RNase L-cleaved RNA and having one or more bases identical to the ligation adapter polynucleotide but not to uncleaved isolated RNA, and a second primer that is identical to at least a portion of the reverse transcription primer;
e) amplifying the cDNA encoding the RNA-ligation adapter polynucleotide product; and
f) detecting the amplified product of (e) to detect a RNase L cleaved RNA product (“RNase L cleavage product”).

2. The method of claim 1 optionally comprising a step of isolating the amplified product prior to the detecting step.

3. The method of claim 1 wherein step (b) can be carried out prior to step (a).

4. The method of claim 1 , wherein the detecting is performed by a method selected from the group consisting of PCR, qPCR, sequencing and DNA gel electrophoresis.

5. The method of claim 1 wherein the small RNAs are less than 200 nucleotides.

6. The method of claim 1 where the first primer
(i) has no bases complementary to the ligation adapter polynucleotide;
(ii) has from 1 to 10 bases complementary to the ligation adapter polynucleotide, but not to the RNA cleaved by RNase L; or
(iii) comprises 1, 2 or 3 nucleotides that are complementary to the ligation adapter polynucleotide sequence.

7. The method of claim 1 wherein the first and second primers consist of between 17 and 24 nucleotides each.

8. The method of claim 1 wherein the ligation adapter polynucleotide is ligated to the isolated RNA with RtcB RNA ligase.

9. The method of claim 1 wherein the ligation adapter polynucleotide has a 2′, 3′ cyclic phosphate or 3′-phosphate and is ligated to the 5′-OH-end of RNA cleaved by RNase L.

10. The method of claim 1 wherein the RNA cleaved by RNase L is labeled with a detectable label.

11. The method of claim 1 wherein the ligation adapter polynucleotide is RNA or an RNA/DNA mixed polynucleotide.

12. The method of claim 1 wherein the ligation adapter polynucleotide has the polynucleotide sequence 5′-GAUCGUCGGACTGTAGAACTCTGAAC-3′ (SEQ ID NO: 1), wherein the first 6 nucleotides are RNA and the remainder of the nucleotides are DNA.

13. The method of claim 1 wherein the RNase L cleavage product results from cleavage of RNA by RNase L between nucleotides that follow a U or a C RNA base, optionally wherein the sequence is UN{circumflex over ( )}N or CN{circumflex over ( )}N.

14. The method of claim 1 wherein the sample is isolated from a subject.

15. The method of claim 14 wherein the subject is suspected of suffering from or is suffering from inflammation or an ongoing immune response.

16. The method of claim 1 wherein the RNase L cleavage product is
(i) a tRNA, rRNA, Y-RNA, snoRNA or vtRNA;
(ii) tRNA-His, tRNA-Gln, tRNA-Glu, tRNA-Lys or tRNA-Pro;
(iii) RNY1, RNY3, RNY4 or RNY5;
(iv) VTRNA1 or VTRNA2; or
(v) RNU1, SNORA1, SNORD16, 28S RNA or 18S rRNA.

17. A method for determining efficacy of an anti-inflammatory treatment in a subject suffering from inflammation comprising detecting RNase L cleavage products in a subject according to the method of claim 1 before and after administration of an anti-inflammatory agent, wherein a decrease in RNase L cleavage products after administration indicates the anti-inflammatory agent is reducing inflammation in the subject.

Assignees

• Univ Princeton

Inventors

• Korennykh Alexei
• Donovan Jesse

Classifications

• C12Q1/44 Primary

  involving esterase · CPC title

• A61P11/06

  Antiasthmatics · CPC title

• A61P25/00

  Drugs for disorders of the nervous system · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title