Overall Section The Mutant Mouse Resource and Research Center (MMRRC) Consortium is the nation?s primary mutant mouse archive and distribution repository system. The MMRRC Consortium was established by the NIH to ensure the preservation, dissemination, and development of valuable mutant mouse strains and data generated by research scientists, and especially now plays a key role in supporting rigor and reproducibility of experimental results using model animals. The MMRRC Consortium was constituted as a trans-national regionally-distributed network of four Centers each hosting an archive and distribution repository, one of which is located at UC Davis (MMRRC-UCD), and an Informatics Coordination and Service Center (ICSC), also coincidentally located at UC Davis. In coordination with other members of the MMRRC Consortium, the MMRRC-UCD serves the needs of the nation?s biomedical research community by ensuring access to and optimizing utilization of transgenic, knockout and other genetically engineered mutant mice and related biomaterials, services, and new technologies. To do so, the MMRRC-UCD imports, verifies, maintains, and distributes mice, gene-targeted embryonic stem (ES) cells, and germplasm of genetically unique, scientifically valuable mice that are essential for contemporary translational biomedical research. The MMRRC-UCD also provide services and procedures to assist investigators using genetically-altered mice for research in numerous areas including cancer, neurodegenerative, metabolic, developmental, genetic, and other diseases. Finally, the MMRRC-UCD conducts resource-related research and develops and refines technologies, that add scientific value to submitted mutant mouse strains, and that capitalize on the power of mouse genetics for biomedical research. By submitting their mice to the MMRRC Consortium, and upon acceptance, assignment, and deposition into the MMRRC-UCD (or any of the other 3 Centers), investigators fulfill their obligation under the NIH Data and Resource Sharing Policies. In return, the MMRRC-UCD strives to preserve, protect, quality control, and provide mouse models for study by research scientists and investigators across the nation and the globe. Through surveys and feedback from our users, discussions with our MMRRC Consortium colleagues and NIH Program representatives, input from our Internal Advisors, and engagement with the MMRRC External Advisory Committee (EAC) of experts, the long-term sustainability and relevance of the MMRRC-UCD to the biomedical research will be assured for years to come.

Public Health Relevance

Overall Section The Mutant Mouse Resource and Research Center (MMRRC) at UC Davis (MMRRC-UCD) is the flagship of the MMRRC Consortim, and serves a leading role in facilitating research by identifying, acquiring, evaluating, characterizing, cryopreserving, and distributing mutant mouse strains to qualified biomedical investigators. The MMRRC-UCD ensures that scientifically valuable transgenic, knockout, and other genetically-engineered mutant mice and related biomaterials of human disease, development, and behavioral abnormalities are maintained for investigational use across the biomedical scientific community. The MMRRC-UCD provides expertise, infrastructure, resources and services to preserve mouse strains in perpetuity, protect them from catastrophic loss, avoid genetic and phenotypic drift, prevent pathogenic contamination and disease, and conduct resource-related research to advance the study of mutant mice as models of human disease, including cancer. The MMRRC-UCD fosters and promotes the discovery of new diagnostics, treatments, and prevention strategies against human diseases, including cancer, optimizes reproducibility of studies, and assures scientific rigor and transparency.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
Animal (Mammalian and Nonmammalian) Model, and Animal and Biological Materials Resource Cooperative Agreements (U42)
Project #
5U42OD012210-22
Application #
10104553
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mirochnitchenko, Oleg
Project Start
1999-09-30
Project End
2025-01-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
22
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of California Davis
Department
Surgery
Type
Schools of Medicine
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
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Hart, Marcia L; Ericsson, Aaron C; Lloyd, K C Kent et al. (2018) Development of outbred CD1 mouse colonies with distinct standardized gut microbiota profiles for use in complex microbiota targeted studies. Sci Rep 8:10107
González-Fernández, Estibaliz; Jeong, Hey-Kyeong; Fukaya, Masahiro et al. (2018) PTEN negatively regulates the cell lineage progression from NG2+ glial progenitor to oligodendrocyte via mTOR-independent signaling. Elife 7:
Wang, Yixin; Jin, Yi; Laviña, Bàrbara et al. (2018) Characterization of multi-cellular dynamics of angiogenesis and vascular remodelling by intravital imaging of the wounded mouse cornea. Sci Rep 8:10672
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Pol, Arjan; Renkema, G Herma; Tangerman, Albert et al. (2018) Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis. Nat Genet 50:120-129
Malenczyk, Katarzyna; Szodorai, Edit; Schnell, Robert et al. (2018) Secretagogin protects Pdx1 from proteasomal degradation to control a transcriptional program required for ? cell specification. Mol Metab :
Ray, Thomas A; Roy, Suva; Kozlowski, Christopher et al. (2018) Formation of retinal direction-selective circuitry initiated by starburst amacrine cell homotypic contact. Elife 7:
Renteria, Rafael; Baltz, Emily T; Gremel, Christina M (2018) Chronic alcohol exposure disrupts top-down control over basal ganglia action selection to produce habits. Nat Commun 9:211
Dahlhaus, Regina (2018) Of Men and Mice: Modeling the Fragile X Syndrome. Front Mol Neurosci 11:41

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