IP Library Granted Patent US 9,393,257
Granted Patent B2
US 9,393,257 · App. 14/193,037 · Granted Jul 19, 2016

TALEN-based gene correction

Inventors: Mark J. Osborn (St. Paul, MN); Jakub Tolar (Minneapolis, MN); Bruce Blazar (Golden Valley, MN); Daniel F. Voytas (Falcon Heights, MN)
Assignee: Regents of the University of Minnesota
A61K31/7088C12N9/16
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Quick Facts
Patent No.
US 9,393,257
App. No.
14/193,037
Granted
Jul 19, 2016
Kind
B2
Abstract

The invention is directed to transcription activator-like effector nuclease (TALEN)-mediated DNA editing of disease-causing mutations in the context of the human genome and human cells to treat patients with compromised genetic disorders.

Claims (13)

1. A composition comprising:

a nucleic acid encoding at least one TALEN protein, wherein the at least one TALEN protein is capable of inducing a site-specific double stranded DNA break in a target gene in a cell, wherein the target gene is a COL7A1 gene; and

a nucleic acid donor sequence,

wherein the donor sequence is a template for correction of a genetic mutation in the Col7A1 target gene, and further wherein the genetic mutation is capable of causing epidermolysis bullosa.

2. The composition of claim 1 , wherein the cell is selected from the group consisting of a fibroblast, keratinocyte, inducible pluripotent stem cell, hematopoietic stem cell, mesenchymal stem cell, embryonic stem cell, hematopoietic progeny cell, T-cell, B-cell, glial cell, neural cell, neuroglial progenitor cell, neuroglial stem cell, muscle cell, lung cell, pancreatic cell, liver cell and a cell of the reticular endothelial system.

3. The composition of claim 1 , wherein the composition comprises a nucleic acid encoding a first TALEN protein which is a left TALEN and the composition compromises a nucleic acid which encodes a second TALEN which is a right TALEN that cooperates with the left TALEN to make a site-specific double stranded DNA break in the target gene.

4. The composition of claim 1 , wherein the nucleic acid encoding the TALEN protein or the nucleic acid donor sequence is part of a vector or plasmid.

5. The composition of claim 3 , wherein the first TALEN and/or the second TALEN comprise a plurality of TAL effector repeat sequences and the endonuclease domain and a spacer between the plurality of TAL effector repeat sequences and the endonuclease domain includes a spacer.

6. The composition of claim 5 , wherein the spacer is 12 to 30 nucleotides in length.

7. A vector comprising the nucleic acid encoding the first TALEN protein of claim 1 .

8. A vector comprising the first nucleic acid and/or the second nucleic acid of claim 3 .

9. The composition of claim 1 , wherein the nucleic acid donor sequence comprises SEQ ID NO: 22.

10. The composition of claim 1 , wherein the nucleic acid sequence encoding the at least one TALEN protein is selected from the group consisting of SEQ ID Nos: 28, 29, 30, 31, and combinations thereof.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2016
From: BLAZAR, BRUCE R.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 038629/0642 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2016
From: VOYTAS, DANIEL F.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 038629/0741 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2016
From: TOLAR, JAKUB
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 038629/0932 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2016
From: OSBORN, MARK J.
To: REGENTS OF THE UNIVERSITY OF MINNESOTA
Reel/Frame 038630/0021 →
CONFIRMATORY LICENSE Recorded Jun 19, 2014
From: REGENTS OF THE UNIVERSITY OF MINNESOTA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 033200/0866 →
Continuity (2)
Provisional Application 61771735 · Mar 1, 2013
Related Publication 20140256798A1 · Sep 11, 2014