Pig model for diabetes

Patent metadata

Field	Value
Publication number	US-10729112-B2
Application number	US-201515506388-A
Country	US
Kind code	B2
Filing date	Aug 28, 2015
Priority date	Aug 28, 2014
Publication date	Aug 4, 2020
Grant date	Aug 4, 2020

Abstract

The present invention relates to a transgenic pig comprising a mutated IAPP gene and displaying a phenotype associated with diabetes. The invention also relates to a transgenic blastocyst, embryo, fetus, donor cell and/or cell nucleus derived from said transgenic pig. The invention further relates to use of the transgenic pig as a model system for studying therapy, treatment and/or prevention of diabetes.

First claim

The invention claimed is:

1. A transgenic pig comprising in its genome a mutated human Islet Amyloid Polypeptide (hIAPP) gene operably linked to a rat insulin promoter wherein said mutated hIAPP gene comprises a mutation resulting in the amino acid substitution S20G of active amylin, as reflected in SEQ ID NO:12 and is inserted into exon 2 of the endogenous IAPP gene of the porcine genome wherein said insertion results in reduction or ablation of the expression of the endogenous IAPP gene and wherein said pig displays at least one phenotype associated with diabetes selected from the group consisting of higher glucose levels, higher glucagon levels, lower insulin levels, and/or lower c-peptide levels when compared to a control pig.

2. The transgenic pig according to claim 1 , wherein said transgenic pig does not express an endogenous pig IAPP gene.

3. The transgenic pig according to claim 2 , wherein said endogenous pig IAPP gene has been knocked out.

4. The transgenic pig according to claim 1 , wherein said transgenic pig is a mini-pig.

5. The transgenic pig according to claim 1 wherein said glucose level and/or said glucagon level is increased by at least 10% when compared to a control pig and wherein said transgenic pig and said control pig are given a normal diet.

6. The transgenic pig according to claim 1 , wherein said insulin level and/or said c-peptide level is decreased by at least 10% when compared to a control pig when said transgenic pig and said control pig are given a normal diet.

7. The transgenic pig according to claim 5 , wherein said control pig does not comprise a mutated IAPP gene.

8. The transgenic pig according to claim 1 , wherein said transgenic pig displays hyperglycemia.

9. The transgenic pig according to claim 1 , wherein said transgenic pig displays β-cell degradation.

10. The transgenic pig according to claim 1 , wherein said transgenic pig displays at least one phenotype selected from the group consisting of blindness, inflammation, infection, and organ deformation.

11. A transgenic blastocyst, embryo, fetus, donor cell and/or cell nucleus derived from the transgenic pig according to claim 1 .

12. A method for producing the transgenic pig according to claim 1 , said method comprising:
i. producing a porcine oocyte having a partially digested zona pellucida,
ii. separating the oocyte into at least two parts obtaining an oocyte having a nucleus and at least one cytoplast,
iii. introducing an expression vector encoding the TALEN pair as set forth in TALEN-1 (SEQ ID NO: 14 and SEQ ID NO: 15) or TALEN-2 (SEQ ID NO: 16 and SEQ ID NO: 17) in a donor pig cell and introducing a targeting vector as set forth in SEQ ID NO: 13 into the genome of a donor pig cell resulting in a porcine donor cell comprising in its genome a mutated hIAPP gene operably linked to a rat insulin promoter, inserted into exon 2 of the endogenous IAPP gene of the porcine genome wherein said mutated hIAPP gene comprises a mutation resulting in the amino acid substitution S20G of active amylin, as reflected in SEQ ID NO: 12,
iv. fusing at least one porcine cytoplast with the donor cell,
v. obtaining a porcine reconstructed embryo,
vi. activating the reconstructed embryo to form an embryo, culturing said embryo, and
vii. transferring said cultured embryo to a porcine host, wherein the embryo develops into a transgenic pig.

13. The method according to claim 12 , wherein said donor cell does not express an endogenous pig IAPP gene.

14. The method according to claim 13 , wherein said endogenous pig IAPP gene has been knocked out.

15. A method for studying therapy, treatment and/or prevention of diabetes comprising the steps of
i. providing a transgenic pig according to claim 1
ii. providing a compound to be tested,
iii. administering said compound to said transgenic pig,
iv. determining one or more risk factors of said transgenic pig associated with diabetes, the one or more risk factors selected from the group consisting of insulin level, glucose level, glucagon level and/or c-peptide level,

thereby determining the effect of said compound on the insulin level, glucose level, glucagon level and/or c-peptide level of said transgenic pig.

16. The transgenic pig according to claim 1 , wherein said mutated hIAPP gene is inserted using a targeting vector.

Assignees

• Univ Aarhus

Inventors

• Bolund Lars
• Luo Yonglun

Classifications

• C07K14/4711

  Alzheimer's disease; Amyloid plaque core protein · CPC title

• C12N15/907

  in mammalian cells · CPC title

• A01K2207/15

  Humanized animals · CPC title

• C12N15/8778

  Swine embryos · CPC title

• G01N33/68

  involving proteins, peptides or amino acids {(involving lipoproteins G01N33/92)} · CPC title