IP Library Granted Patent US 8,502,018
Granted Patent B2
US 8,502,018 · App. 13/164,176 · Granted Aug 6, 2013

Methods of modifying eukaryotic cells

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Quick Facts
Patent No.
US 8,502,018
App. No.
13/164,176
Granted
Aug 6, 2013
Kind
B2
Abstract

A method for engineering and utilizing large DNA vectors to target, via homologous recombination, and modify, in any desirable fashion, endogenous genes and chromosomal loci in eukaryotic cells. These large DNA targeting vectors for eukaryotic cells, termed LTVECs, are derived from fragments of cloned genomic DNA larger than those typically used by other approaches intended to perform homologous targeting in eukaryotic cells. Also provided is a rapid and convenient method of detecting eukaryotic cells in which the LTVEC has correctly targeted and modified the desired endogenous gene(s) or chromosomal locus (loci) as well as the use of these cells to generate organisms bearing the genetic modification.

Claims (23)

1. A genetically modified mouse, comprising in its germline human unrearranged variable region gene segments inserted at an endogenous mouse immunoglobulin locus.

2. The mouse of claim 1 , wherein the human unrearranged variable region gene segments are heavy chain gene segments, and the mouse immunoglobulin locus is a heavy chain locus.

3. The mouse of claim 1 , wherein the human unrearranged variable region gene segments are light chain gene segments, and the mouse immunoglobulin locus is a light chain locus.

4. The mouse of claim 3 , wherein the light chain gene segments are human kappa light chain gene segments.

5. The mouse of claim 1 , wherein the unrearranged variable region gene segments are contained on a genomic DNA fragment larger than 20 kb.

6. The mouse of claim 1 , wherein the human variable region gene segments are capable of rearranging to form a functional V region gene.

7. The mouse of claim 1 , where following rearrangement the mouse expresses a functional antigen-binding molecule encoded by the human gene segments.

8. The mouse of claim 1 , wherein rearrangement of the human variable gene segments in the mouse results in a variable region gene that comprises a rearranged human variable region gene linked to a mouse constant region gene.

9. The mouse of claim 1 , wherein the mouse produces an antibody that comprises a human variable region and a mouse constant region.

10. The mouse of claim 1 , wherein the mouse does not comprise a human immunoglobulin constant gene.

11. A genetically modified mouse, comprising in its germline human unrearranged variable region gene segments linked to a mouse constant region gene, wherein the mouse lacks a human constant region gene, and wherein the mouse constant region gene is at an endogenous mouse immunoglobulin locus.

12. The mouse of claim 11 , wherein the human unrearranged variable region gene segments are heavy chain gene segments.

13. The mouse of claim 11 , wherein the human unrearranged variable region gene segments are light chain gene segments.

14. The mouse of claim 13 , wherein the light chain gene segments are human kappa light chain gene segments.

15. The mouse of claim 11 , wherein the unrearranged variable region gene segments are contained on a genomic DNA fragment larger than 20 kb.

16. The mouse of claim 11 , wherein the human variable region gene segments are capable of rearranging to form a functional variable region gene.

17. The mouse of claim 11 , where following rearrangement the mouse expresses a functional antigen-binding molecule encoded by the human gene segments.

18. The mouse of claim 11 , wherein rearrangement of the human variable gene segments in the mouse results in a variable region gene that comprises a rearranged human variable region gene operably linked to a mouse constant region gene.

19. The mouse of claim 11 , wherein the mouse produces an antibody that comprises a human variable region and a mouse constant region.

20. A mouse, comprising a modification in the germline of the mouse, wherein the modification comprises

(a) a hybrid heavy chain locus comprising an insertion of human immunoglobulin heavy chain V, D, and J gene segments, wherein the human heavy chain immunoglobulin V, D, and J gene segments are linked to a mouse immunoglobulin heavy chain gene, wherein the mouse immunoglobulin heavy chain gene is at an endogenous mouse immunoglobulin locus;

(b) a hybrid light chain locus comprising an insertion of human immunoglobulin light chain V and J gene segments, wherein the human V and J gene segments are linked to a mouse immunoglobulin light chain constant region gene sequence;

wherein (a) rearranges to form a hybrid heavy chain sequence comprising a human variable region linked to a mouse constant region, and (b) rearranges to form a hybrid light chain sequence comprising a human variable region linked to a mouse constant region, and wherein the mouse is incapable of forming an antibody that comprises a human variable region and a human constant region.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR: ECOMOMIDES, ARIS N. PREVIOUSLY RECORDED ON REEL 032020 FRAME 0441. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNOR: ECONOMIDES, ARIS N.. Recorded Jan 30, 2014
From: ECONOMIDES, ARIS N.; VALENZUELA, DAVID M.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 032137/0537 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2014
From: ECOMOMIDES, ARIS N.; VALENZUELA, DAVID M.
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 032020/0441 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2013
From: KAROW, MARGARET; MACDONALD, LYNN; STEVENS, SEAN
To: REGENERON PHARMACEUTICALS, INC.
Reel/Frame 030580/0490 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2013
From: MURPHY, ANDREW J.; YANCOPOULOS, GEORGE D.
To: REGENERON PHARMACEUTICALS INC.
Reel/Frame 030068/0356 →