IP Library Granted Patent US 12662671
Granted Patent B2
US 12662671 · App. 18/587,710 · Granted Jun 23, 2026

Constructs and methods for preparing circular RNA

Inventors: Wensheng Wei (Beijing, CN); Zongyi Yi (Beijing, CN)
Assignee: PEKING UNIVERSITY
C12N15/113C12N15/52C12N2770/32343
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Quick Facts
Patent No.
US 12662671
App. No.
18/587,710
Granted
Jun 23, 2026
Kind
B2
Abstract

The present application provides linear RNA precursors and constructs for preparing circular RNAs (circRNAs) comprising an effector RNA sequence, such as a coding RNA sequence. In some embodiments, the linear RNA comprises from the 5′ end to the 3′ end: (a) a first portion of an RNA element (e.g., an IRES), (b) an effector RNA sequence, and (c) a second portion of the RNA element, wherein the first and the second portions of the RNA element associate with each other to form a double-stranded region of at least 4 basepairs long, wherein 5′ end of the first portion of the RNA element and 3′ end of the second portion of the RNA element form a nick in the double-stranded region, and wherein an RNA ligase can ligate the nick. Also provided are methods of preparing circRNAs, circRNAs prepared thereof, and methods of using the circRNAs.

Claims (30)

1 . A linear RNA, comprising from the 5′ end to the 3′ end:

(a) a first portion of an RNA element;

(b) an effector RNA sequence; and

(c) a second portion of the RNA element;

wherein the RNA element is an internal ribosomal entry site (IRES) or a portion thereof;

wherein the first portion of the RNA element and the second portion of the RNA element associate with each other to form a double-stranded region of at least 4 basepairs (bp) long;

wherein the 5′ end of the first portion of the RNA element and the 3′ end of the second portion of the RNA element form a nick in the double-stranded region; and

wherein the nick can be ligated by an RNA ligase.

2 . The linear RNA of claim 1 , wherein the double-stranded region is about 6 bp long to about 25 bp long.

3 . The linear RNA of claim 1 , wherein the RNA element is at least 20 nt long.

4 . The linear RNA of claim 1 , wherein the double-stranded region comprises at least 2 bp 3′ to the nick, and/or the double-stranded region comprises at least 2 bp 5′ to the nick.

5 . The linear RNA of claim 1 , wherein the first portion of the RNA element and/or the second portion of the RNA element comprises a sequence that is exogenous to the reference RNA element.

6 . The linear RNA of claim 1 , wherein the second portion of the RNA element comprises a first exogenous sequence at the 3′ end, wherein the first portion of the RNA element comprises a second exogenous sequence that is complementary of the first exogenous sequence, and wherein the first exogenous sequence and the second exogenous sequence form base pairs flanking the 5′ end of the nick.

7 . The linear RNA of claim 1 , wherein the effector RNA sequence is a coding RNA sequence.

8 . The linear RNA of claim 7 , wherein the coding RNA sequence encodes a therapeutic polypeptide.

9 . The linear RNA of claim 1 , wherein the IRES is derived from:

(a) an IRES selected from the group consisting of Coxsackievirus B3 (CVB3) IRES, Enterovirus 71 (EV71) IRES, encephalomyocarditis virus (EMCV) IRES, picornavirus (PV) IRES, hepatitis C virus (HCV) IRES, adenovirus (AdV) IRES, human papillomavirus type 31 (HPV31) IRES, human herpesvirus (HHV) IRES, Rous sarcoma virus (RSV) IRES, and classical swine fever virus (CSFV) IRES; or

(b) an IRES selected from the group consisting of FGF9 IRES, SLC7A1 IRES, and RUNX1 IRES.

10 . The linear RNA of claim 9 , wherein the IRES is an IRES of a CVB3 virus or a derivative thereof.

11 . The linear RNA of claim 10 , wherein the IRES of a CVB3 virus comprises the nucleotide sequence of SEQ ID NO: 1.

12 . The linear RNA of claim 11 , wherein the first portion of the RNA element comprises nucleotides 382-741 of SEQ ID NO: 1, and wherein the second portion of the RNA element comprises nucleotides 1-381 of SEQ ID NO: 1.

13 . The linear RNA of claim 12 , wherein the first portion of the RNA element comprises the nucleotide sequence of SEQ ID NO: 3, and wherein the second portion of the RNA element comprises the nucleotide sequence of SEQ ID NO: 2.

14 . The linear RNA of claim 11 , wherein the first portion of the RNA element comprises nucleotides 343-741 of SEQ ID NO: 1, and wherein the second portion of the RNA element comprises nucleotides 1-342 of SEQ ID NO: 1.

15 . The linear RNA of claim 7 , further comprising an in-frame 2A peptide coding sequence that is operably linked to the 3′ end of the coding RNA.

16 . The linear RNA of claim 1 , wherein the effector RNA sequence is a sequence of a non-coding RNA selected from the group consisting of a guide RNA (gRNA), a deaminase-recruiting RNA (dRNA), a siRNA, a miRNA, a shRNA, and a long intervening non-coding (line) RNA.

17 . A method of preparing a circRNA, comprising:

(a) contacting the linear RNA of claim 1 with a RNA ligase under conditions that allow ligation of the nick in the linear RNA to provide a circularized RNA product; and

(b) isolating the circularized RNA product, thereby providing the circRNA.

18 . A circRNA formed by ligation of the nick in the linear RNA of claim 1 .

19 . A nucleic acid construct comprising a nucleic acid sequence encoding the linear RNA of claim 1 .