IP Library Granted Patent US 7,429,690
Granted Patent B2
US 7,429,690 · App. 10/705,519 · Granted Sep 30, 2008

Transgenic bovines having reduced prion protein production

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Quick Facts
Patent No.
US 7,429,690
App. No.
10/705,519
Granted
Sep 30, 2008
Kind
B2
Abstract

The invention provides cloned transgenic ungulates (e.g., bovines) in which prion protein activity is reduced by one or more genetically engineered mutations. Desirably, these transgenic bovines are also genetically modified to express xenogenous (e.g., human) antibodies. Because of their resistance to prion-related diseases such as bovine spongiform encephalopy (also known as mad cow disease), these bovines are a safer source of human antibodies for pharmaceutical uses and a safer source of agricultural products.

Claims (19)

1. A bovine whose genome comprises a non-naturally occurring mutation in one or both alleles of an endogenous prion nucleic acid, wherein said mutation comprises a transcriptional termination sequence, and wherein said bovine exhibits reduced functional prion production.

2. The bovine of claim 1 , wherein said mutation is heterozygous.

3. The bovine of claim 1 , wherein said mutation is homozygous and said bovine exhibits no functional prion production.

4. The bovine of claim 1 , wherein said mutation comprises an insertion of a positive selection marker into a prion nucleic acid.

5. The bovine of claim 1 , wherein said mutation comprises a deletion of one or more nucleotides in a prion nucleic acid.

6. An isolated bovine cell comprising a non-naturally occurring mutation in one or both alleles of an endogenous prion nucleic acid, wherein said mutation comprises a transcriptional termination sequence, and wherein said bovine cell exhibits reduced functional prion production.

7. The cell of claim 6 , wherein said mutation is heterozygous.

8. The cell of claim 6 , wherein said mutation is homozygous and said bovine cell exhibits no functional prion production.

9. The cell of claim 6 , wherein said cell is a fetal fibroblast.

10. The cell of claim 6 , wherein said cell is a B-cell.

11. A method for producing an isolated transgenic bovine cell having reduced expression of functional prion protein, comprising

(a) introducing a first prion gene targeting vector into a bovine fibroblast cell under conditions that allow homologous recombination between said first vector and a first allele of an endogenous prion nucleic acid in said cell, thereby introducing a heterozygous mutation in said cell, wherein said mutation comprises a transcriptional termination sequence and a selectable marker;

(b) isolating said fibroblast cell containing the heterozygous mutation; and

(c) introducing a second prion gene targeting vector having a different selectable marker than said first vector into said bovine cell of step (b) under conditions that allow homologous recombination between said second vector and a second allele of an endogenous prion nucleic acid in said cell, thereby introducing a homologous mutation in said bovine cell.

12. The method of claim 11 , wherein said bovine fibroblast cell is a bovine fetal fibroblast cell.

13. A method for producing a transgenic bovine having reduced expression of functional prion protein, said method comprising the steps of:

(a) inserting a diploid permeabilized cell into an enucleated metaphase II oocyte, wherein said cell comprises a first non-naturally occurring mutation in an endogenous prion nucleic acid wherein said mutation comprises a transcriptional termination sequence; and

(b) transferring said oocyte or an embryo formed from said oocyte into the uterus of a host bovine under conditions that allow said oocyte or said embryo to develop into a fetus, wherein the genome of said fetus comprises said non-naturally occurring mutation in said endogenous prion nucleic acid and wherein said fetus exhibits reduced functional prion production.

14. The method of claim 13 , wherein said fetus develops into a viable offspring.

Assignments (11)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2019
From: SAB BIOTHERAPEUTICS, INC.
To: SAB LLC
Reel/Frame 048511/0975 →
ASSET CONTRIBUTION AND ASSUMPTION OF LIABILITIES AGREEMENT Recorded Feb 13, 2019
From: BIODAK LLC
To: SAB BIOTHERAPEUTICS, INC.
Reel/Frame 048326/0877 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 24, 2011
From: KYOWA HAKKO KIRIN CO., LTD.
To: BIODAK, LLC
Reel/Frame 026495/0001 →
MERGER Recorded Dec 23, 2008
From: KIRIN PHARMA KABUSHIKI KAISHA
To: KYOWA HAKKO KIRIN CO., LTD.
Reel/Frame 022021/0606 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2008
From: KIRIN HOLDINGS KABUSHIKI KAISHA
To: KIRIN PHARMA KABUSHIKI KAISHA
Reel/Frame 021508/0274 →
CHANGE OF NAME Recorded Mar 20, 2008
From: KIRIN BEER KABUSHIKI KAISHA
To: KIRIN HOLDINGS KABUSHIKI KAISHA
Reel/Frame 020686/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2007
From: HEMATECH, LLC
To: KIRIN BEER KABUSHIKI KAISHA
Reel/Frame 019799/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2007
From: HEMATECH, LLC
To: KIRIN BEER KABUSHIKI KAISHA
Reel/Frame 019020/0187 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 29, 2005
From: COLLAS, PHILIPPE
To: HEMATECH, LLC
Reel/Frame 016677/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2004
From: KUROIWA, YOSHIMI; TOMIZUKA, KAZUMA; ISHIDA, ISAO
To: KIRIN BEER KABUSHIKI KAISHA
Reel/Frame 015331/0986 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2004
From: ROBL, JAMES M.; SULLIVAN, EDDIE; KASINATHAN, POOTHAPPILLAI
To: HEMATECH, LLC
Reel/Frame 015332/0334 →