Rna and dna base editing via engineered adar recruitment
AssigneeThe Regents of the University of California
InventorsPrashant Mali, Dhruva Katrekar, Dario Meluzzi, Genghao Chen, Kyle M. Ford
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Abstract
Disclosed herein is a system to recruit ADARs to catalyze therapeutic editing of point mutations via the use of engineered RNA scaffolds, engineered DNA scaffolds or DNA-RNA hybrid scaffolds. The system comprises an engineered ADAR2 guide RNA (adRNA) that bears a 20-100 bp complementarity with the target RNA and ADAR2 recruiting domain from the GluR2 mRNA at either or both 5′ end or 3′ end.
Claims19
A vector comprising a nucleic acid encoding an engineered guide RNA that comprises a sequence complementary to a target RNA that, upon hybridizing to the target RNA, forms a double stranded RNA comprising a mismatch, wherein the double stranded RNA recruits an endogenous adenosine deaminase acting on RNA 1 (ADAR1) or an endogenous ADAR2 that edits the target RNA;
- wherein the engineered guide RNA has a length of from 15±10% to 200±10% nucleotides, wherein:
- (a) the hybridization to the target RNA is configured to form a complex that is stabilized by hydrogen bonding between bases of the target RNA and the engineered guide RNA, wherein at least one base pair hydrogen bonding is not a Watson-Crick base pair hydrogen bond;
- or
- (b) the edit of the target RNA results in a decrease of an expression of a polypeptide encoded by the target RNA;
- or
- (c) any combination of (a) and (b);
- wherein the engineered guide RNA does not have an ADAR recruiting domain, and wherein the vector does not encode or contain an exogenous ASAR enzyme.
A method of treating a disease or condition in a subject in need thereof, the method comprising administering to the subject a pharmaceutical composition, wherein the pharmaceutical composition comprises:
- a vector comprising a nucleic acid encoding an engineered guide RNA that comprises a sequence complementary to a target RNA that, upon binding to the target RNA, forms a double stranded RNA comprising a mismatch, wherein the double stranded RNA recruits an endogenous adenosine deaminase acting on RNA 1 (ADAR1) or an endogenous ADAR2 that edits the target RNA;
- wherein the engineered guide RNA has a length of from 15±10% to 200±10% nucleotides, wherein:
- (a) the hybridization to the target RNA is configured to form a complex that is stabilized by hydrogen bonding between bases of the target RNA and the engineered guide RNA, wherein at least one base pair hydrogen bonding is not a Watson-Crick base pair hydrogen bond;
- or
- (b) the edit of the target RNA results in a decrease of an expression of a polypeptide encoded by the target RNA;
- or
- (c) any combination of (a) and (b);
- wherein the engineered guide RNA does not have an ADAR recruiting domain, wherein the pharmaceutical composition does not encode or contain an exogenous ADAR enzyme, and wherein the pharmaceutical composition is administered in an amount sufficient to treat the disease or condition.
A vector that comprises a nucleic acid with a polynucleotide sequence encoding at least one RNA editing entity recruiting domain, wherein:
- (i) the polynucleotide sequence encoding the at least one RNA editing entity recruiting domain lacks a secondary structure comprising a stem-loop, or
- (ii) the polynucleotide sequence encoding the at least one RNA editing entity recruiting domain comprises at least about 80% sequence identity to at least one sequence selected from:
- an Alu domain encoding sequence, an Apolipoprotein B mRNA Editing Catalytic Polypeptide-like (APOBEC) recruiting domain encoding sequence, and combination thereof.
A vector comprising a nucleic acid encoding for RNA with a two dimensional shape that is substantially a cruciform, wherein the RNA comprises at least one sequence encoding an RNA editing entity recruiting domain.
Dependencies are inferred from the claim text.