Enzymatic methods to generate high yields of sequence specific RNAs with extreme precision

Patent metadata

Field	Value
Publication number	US-12359248-B2
Application number	US-202117512975-A
Country	US
Kind code	B2
Filing date	Oct 28, 2021
Priority date	Apr 24, 2019
Publication date	Jul 15, 2025
Grant date	Jul 15, 2025

Abstract

Described herein are synthetic methods for producing sequence-specific RNA oligonucleotides that eliminate impurities produced in prior art methods. In one aspect, a first amplification primer includes one or more deoxyuridine residues, wherein at least one of the one or more deoxyuridine residues is at position −1, −2, −3, −4 or −5 of the promoter region for the single-subunit, DNA-dependent RNA polymerase. The deoxyuridines are excised to provide an amplified functional template DNA which is then used to synthesize RNA which has reduced immunogenic double stranded RNA compared to controls.

First claim

The invention claimed is:

1. A method of synthesizing RNA, comprising,
providing a starting functional template DNA for a single-subunit, DNA-dependent RNA polymerase, and first and second amplification primers for the starting functional template DNA, wherein the starting functional template DNA comprises a promoter region for the single-subunit, DNA-dependent RNA polymerase,
wherein the first amplification primer is complementary to a template strand of the template DNA and comprises one or more deoxyuridine residues, wherein at least one of the one or more deoxyuridine residues is at position −1, −2, −3, −4 or −5 of the promoter region for the single-subunit, DNA-dependent RNA polymerase, and
wherein the second amplification primer is complementary to a nontemplate strand of the template DNA;

amplifying the starting functional template DNA in the presence of the first and second amplification primers and under conditions for DNA amplification to provide an amplified functional template DNA, wherein the amplified functional template DNA comprises the one or more deoxyuridine residues at position −1, −2, −3, −4 or −5 of the promoter region for the single-subunit, DNA-dependent RNA polymerase;
excising the uracil bases of the deoxyuridine residues from the promoter region of the amplified functional template DNA to provide a modified, amplified functional template DNA;
carrying out a transcription reaction to synthesize RNA from the modified, amplified functional template DNA in the presence of the single-subunit, DNA-dependent RNA polymerase and under conditions for RNA synthesis; and
isolating the synthesized RNA from the transcription reaction.

2. The method of claim 1 , wherein the first amplification primer comprises one deoxyuridine residue at position −1, −2, −3, −4 or −5 of the promoter region for the single-subunit, DNA-dependent RNA polymerase.

3. The method of claim 1 , wherein at least one of the one or more deoxyuridine residues is at position −4 or −5 of the promoter region.

4. The method of claim 1 , wherein RNA synthesis is conducted under high salt conditions of 50 to 1000 mM.

5. The method of claim 1 , wherein excising the uracil bases of the deoxyuridine residues comprises treating with DNA glycosylase, an exonuclease, or a combination thereof, to create a nick, break or gap in the nontemplate strand of the modified, amplified functional template DNA.

6. The method of claim 1 , wherein the single-subunit, DNA-dependent RNA polymerase comprises a T7 RNA polymerase, a T3 RNA polymerase, a K11 RNA polymerase, an SP6 RNA polymerase, or a Syn5 RNA polymerase.

7. The method of claim 1 , wherein the synthesized RNA has a length of 10 to 10,000 bases.

8. The method of claim 1 , wherein the synthesized RNA is an mRNA, a CRISPR RNA, or a lncRNA.

9. The method of claim 1 , wherein the isolated, synthesized RNA has at least a 5-fold reduction in binding to an immunogenic dsRNA-specific antibody compared to a control synthesized RNA synthesized from a control template DNA having a template strand identical to the template strand of the modified, amplified functional template DNA and a non-template strand that does not have a missing base, nick, break or gap in the promoter region.

Assignees

• Univ Massachusetts
• Univ Massachusetts

Inventors

• Martin Craig
• Cavac Elvan
• Malagodapathiranage Kithmie Harshana

Classifications

• C12Q1/6853

  using modified primers or templates · CPC title

• C12Q1/6848 Primary

  characterised by the means for preventing contamination or increasing the specificity or sensitivity of an amplification reaction · CPC title

• C12Q1/6844 Primary

  Nucleic acid amplification reactions · CPC title