IP Library Granted Patent US 9,578,859
Granted Patent B2
US 9,578,859 · App. 14/989,134 · Granted Feb 28, 2017

Transgenic mice expressing human pyrin domain only protein 2

Inventor: Jonathan A. Harton (Slingerland, NY)
Assignee: ALBANY MEDICAL COLLEGE
A01K67/0278C12N15/8509A01K2207/15A01K2227/105A01K2267/0368C12N2015/8527
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Quick Facts
Patent No.
US 9,578,859
App. No.
14/989,134
Granted
Feb 28, 2017
Kind
B2
Abstract

A transgenic mouse expressing the human gene for PYRIN domain-only protein 2 (POP2). POP2, when expressed in the transgenic mouse model, broadly dampens inflammatory cytokine production, in part through restricting the activation of both Nlrp3 and Aim2 inflammasomes. POP2 mice exhibit reduced susceptibility to LPS- and bacteria-induced septic shock. Further, POP2 mice are less susceptible to the fatal, acute inflammatory pneumonia caused by pulmonary infection with F. tularensis LVS and F. novicida , which are highly pathogenic to mice, but non-pathogenic to humans.

Claims (12)

1. A transgenic mouse whose genome comprises a human pyrin-domain only protein 2 (POP2) transgene comprising 2000 base pairs upstream of a human POP2 gene coding region, a single POP2 exon coding sequence, and a 3′ untranslated region sequence, wherein the mouse expresses the POP2 transgene and has a phenotype of reduced production of proinflammatory cytokines in response to LPS-induced shock and bacterial infections when compared to a control mouse.

2. The transgenic mouse of claim 1 , wherein the tissue expression pattern of the POP2 gene in the mouse is consistent with the tissue expression pattern of the POP2 gene in a human.

3. The transgenic mouse of claim 2 , wherein the transgene comprises SEQ ID NO: 1.

4. The transgenic mouse of claim 3 , wherein the genome of the mouse is on a C57BL/6 background.

5. A method of producing a transgenic mouse, comprising the steps of:

microinjecting a human pyrin-domain only protein 2 (POP2) transgene comprising 2000 base pairs upstream of a human POP2 gene coding region, a single POP2 exon coding sequence, and a 3′ untranslated region sequence into a fertilized mouse oocyte;

transferring said fertilized oocyte to a pseudopregnant female mouse;

allowing said transferred fertilized oocyte to develop to term; and

identifying and selecting a transgenic mouse whose genome comprises the POP2 transgene and has a phenotype of reduced production of proinflammatory cytokines in response to LPS-induced shock and bacterial infections when compared to a control mouse.

6. The method of claim 5 , wherein the tissue expression pattern of the POP2 gene in the mouse is consistent with the tissue expression pattern of the POP2 gene in a human.

7. The method of claim 6 , wherein the transgene comprises SEQ ID NO: 1.

8. The method of claim 7 , wherein the genome of the transgenic mouse is on a C57BL/6 background.

Assignments (3)
CONFIRMATORY LICENSE Recorded Jan 19, 2017
From: ALBANY MEDICAL COLLEGE
To: NIH
Reel/Frame 041019/0655 →
CONFIRMATORY LICENSE Recorded Jan 13, 2017
From: ALBANY MEDICAL COLLEGE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041355/0872 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2016
From: HARTON, JONATHAN A.
To: ALBANY MEDICAL COLLEGE
Reel/Frame 037420/0526 →
Continuity (2)
Provisional Application 62100104 · Jan 6, 2015
Related Publication 20160192627A1 · Jul 7, 2016