Advances in genetic technologies allow scientists to routinely create genetically-engineered mice (GEM). GEM have proven extremely valuable in determining the molecular basis of human disease and have been pivotal in development of successful therapeutic strategies. However, thousands of GEM have been created and their numbers continue to increase exponentially. Currently, existing mouse repositories and scientists developing GEM are unable to meet the demands of the biomedical research community. This restricted availability of GEM impedes biomedical research, wastes the scientific and financial resources used to create the GEM and may result in loss of invaluable animal models. The overall goals of this application are to address this issue by establishing mutant mouse regional resource center (MMRRC) that will: (1) import, rederive and produce high-quality GEM, (2) cryopreserve and store GEM germplasm, (3) distribute locally, regionally, and nationally high quality, well characterized GEM to investigators, either as live mice or as crypreserved germplasm, (4) perform genotyping, phenotyping and infectious disease surveillance of GEM strains, and (5) perform innovative research that generates new information that will benefit the community of GEM users. To accomplish this goal, an established, multidisciplinary consortium (Harlan Sprague Dawley, Inc. Indiana University, University of Missouri) will develop a MMRRC primarily located at a Harlan facility in Indianapolis, IN. This unique regional consortium has the infrastructure and expertise in each of the disciplines needed, including importation, quarantine, rederivation, breeding, embryo and gamete cryopreservation, genotyping, phenotyping, infectious disease monitoring, and distribution of mice. The MMRRC will form a cooperative network with other MMRRCs, the MMRRC Advisory Panel (MMRRCAP), and the Informatics Coordinating Center (ICC) to share information. An electronic database, compatible with ICC requirements will be used to share inventory information and quality assurance data. Research projects aimed at improving the efficiency of cryobiology, reconstitution, GEM characterization, and infectious disease monitoring of GEM will be performed. Results of these research investigations will be beneficial to this MMRRC, other MMRRCs and to GEM investigators worldwide.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Animal (Mammalian and Nonmammalian) Model, and Animal and Biological Materials Resource Cooperative Agreements (U42)
Project #
1U42RR014821-01
Application #
6053581
Study Section
Special Emphasis Panel (ZRR1-CM-7 (01))
Program Officer
Mirochnitchenko, Oleg
Project Start
2000-05-01
Project End
2005-04-30
Budget Start
2000-05-01
Budget End
2001-04-30
Support Year
1
Fiscal Year
2000
Total Cost
$980,830
Indirect Cost
Name
Harlan Sprague Dawley, Inc.
Department
Type
DUNS #
City
Indianapolis
State
IN
Country
United States
Zip Code
46229
Benson, James D; Benson, Charles T; Critser, John K (2014) Mathematical model formulation and validation of water and solute transport in whole hamster pancreatic islets. Math Biosci 254:64-75
Kashuba, Corinna M; Benson, James D; Critser, John K (2014) Rationally optimized cryopreservation of multiple mouse embryonic stem cell lines: I--Comparative fundamental cryobiology of multiple mouse embryonic stem cell lines and the implications for embryonic stem cell cryopreservation protocols. Cryobiology 68:166-75
Kashuba, Corinna M; Benson, James D; Critser, John K (2014) Rationally optimized cryopreservation of multiple mouse embryonic stem cell lines: II--Mathematical prediction and experimental validation of optimal cryopreservation protocols. Cryobiology 68:176-84
Rosenfeld, Cheryl S; Sieli, Paizlee T; Warzak, Denise A et al. (2013) Maternal exposure to bisphenol A and genistein has minimal effect on A(vy)/a offspring coat color but favors birth of agouti over nonagouti mice. Proc Natl Acad Sci U S A 110:537-42
Agca, Yuksel (2012) Genome resource banking of biomedically important laboratory animals. Theriogenology 78:1653-65
Benson, James D; Chicone, Carmen C; Critser, John K (2012) Analytical optimal controls for the state constrained addition and removal of cryoprotective agents. Bull Math Biol 74:1516-30
Korampally, Venumadhav; Mamidi, Vamshi Krishna; Harris, Bryant et al. (2011) Sub-minute formation of supported nanoporous mesoscale patterns programmed by surface energy. J Colloid Interface Sci 364:546-54
Benson, James D; Chicone, Carmen C; Critser, John K (2011) A general model for the dynamics of cell volume, global stability, and optimal control. J Math Biol 63:339-59
Hillhouse, Andrew E; Myles, Matthew H; Taylor, Jeremy F et al. (2011) Quantitative trait loci in a bacterially induced model of inflammatory bowel disease. Mamm Genome 22:544-55
Han, Xu; Liu, Yang; Critser, John K (2010) Determination of the quaternary phase diagram of the water-ethylene glycol-sucrose-NaCl system and a comparison between two theoretical methods for synthetic phase diagrams. Cryobiology 61:52-7

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