IP Library Granted Patent US 11,254,930
Granted Patent B2
US 11,254,930 · App. 17/366,290 · Granted Feb 22, 2022

Methods for targeted insertion of DNA in genes

Inventor: Nicholas J. Baltes (Oakdale, MN)
Assignee: BLUEALLELE CORPORATION
C12N15/102C12N15/907C12N2310/20C12N2800/80
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Quick Facts
Patent No.
US 11,254,930
App. No.
17/366,290
Granted
Feb 22, 2022
Kind
B2
Abstract

Methods and compositions for modifying the coding sequence of endogenous genes using rare-cutting endonucleases and transposases. The methods and compositions described herein can be used to modify the coding sequence of endogenous genes.

Claims (27)

1. A recombinant nucleic acid comprising a transgene, the transgene comprising in 5′ to 3′ orientation:

a first splice acceptor, a first coding sequence, a first terminator, a second terminator reverse complement, a second coding sequence reverse complement, and a second splice acceptor reverse complement,

wherein the first coding sequence encodes an amino acid sequence, and the second coding sequence encodes the same amino acid sequence as the first coding sequence.

2. The recombinant nucleic acid of claim 1 , wherein the first coding sequence and second coding sequence comprise different polynucleotide sequences, but each encodes the same amino acid sequence.

3. A recombinant non-viral vector comprising the recombinant nucleic acid of claim 1 .

4. A recombinant viral vector comprising the recombinant nucleic acid of claim 1 .

5. The viral vector of claim 4 , wherein the viral vector is selected from the group consisting of an adenovirus vector, an adeno-associated virus vector, and a lentivirus vector.

6. The recombinant nucleic acid of claim 1 , wherein the first coding sequence and second coding sequence each encode a peptide produced by exon 10 of a non-pathogenic ATXN3 gene.

7. The recombinant nucleic acid of claim 1 , wherein the first coding sequence and second coding sequence each encode a peptide produced by exon 47 of a non-pathogenic CACNA1A gene.

8. The recombinant nucleic acid of claim 1 , wherein the first coding sequence and second coding sequence each encode a peptide produced by a gene selected from Factor V, Factor VII, Factor XIII, Factor IX, Factor X, Factor XI, Factor XII, Factor XIII, an LDL Receptor, and TTR.

9. The recombinant nucleic acid of claim 1 , wherein the recombinant nucleic acid is equal to or less than 4.7 kb.

10. A cell comprising a transgene, wherein the transgene is integrated into an endogenous gene, said transgene comprising in 5′ to 3′ orientation:

a first splice acceptor, a first coding sequence, a first terminator, a second terminator reverse complement, a second coding sequence reverse complement, and a second splice acceptor reverse complement,

wherein the first coding sequence encodes an amino acid sequence heterologous to the cell, and the second coding sequence encodes the same heterologous amino acid sequence.

11. The cell of claim 10 , wherein the first coding sequence or second coding sequence of the transgene is operably linked to a promoter of the endogenous gene.

12. The cell of claim 11 , wherein the first coding sequence and second coding sequence of the transgene comprise different polynucleotide sequences, but each encodes the same heterologous amino acid sequence.

13. The cell of claim 11 , wherein the first coding sequence and second coding sequence each encode a peptide selected from Factor V, Factor VII, Factor XIII, Factor IX, Factor X, Factor XI, Factor XII, Factor XIII, an LDL Receptor, and TTR.

14. The cell of claim 11 , wherein the first coding sequence and second coding sequence each encode a peptide produced by exon 10 of a non-pathogenic ATXN3 gene.

15. The cell of claim 11 , wherein the first coding sequence and second coding sequence each encode a peptide produced by exon 47 of a non-pathogenic CACNA1A gene.

16. A recombinant nucleic acid comprising a transgene, the transgene comprising in 5′ to 3′ orientation:

a first splice acceptor, a first coding sequence, a first terminator, a second terminator reverse complement, a second coding sequence reverse complement, and a second splice acceptor reverse complement,

wherein the first coding sequence encodes an amino acid sequence, and the second coding sequence encodes the same amino acid sequence as the first coding sequence, and

wherein the recombinant nucleic acid is linear or circular.

17. The recombinant nucleic acid of claim 16 , wherein the nucleic acid is in a circular conformation.

18. The recombinant nucleic acid of claim 16 , wherein the first coding sequence and second coding sequence comprise different polynucleotide sequences, but each encodes the same amino acid sequence.

19. A viral vector comprising the recombinant nucleic acid of claim 16 .

20. The viral vector of claim 19 , wherein the viral vector is selected from the group consisting of an adenovirus vector, an adeno-associated virus vector, and a lentivirus vector.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2022
From: BALTES, NICHOLAS
To: BLUEALLELE CORPORATION
Reel/Frame 059666/0983 →
Continuity (6)
Continuation 16800444 · Feb 25, 2020
Continuation 16601144 · Oct 14, 2019
Provisional Application 62864432 · Jun 20, 2019
Provisional Application 62830654 · Apr 8, 2019
Provisional Application 62746497 · Oct 16, 2018
Related Publication 20210332347A1 · Oct 28, 2021
Cited By (2)
US 12,214,023 US 12,441,994