For decades, the mouse has been the premier animal model for studies of human disease, providing the opportunity to explore experimental questions that are intractable for direct study in humans. As a result, key insights have been obtained for a variety of clinical conditions. Spurred by advances in technology and international efforts to systematically knock out all of the protein coding genes in the genome, the number of genetically engineered mice has expanded rapidly in the past 20 years. The responsibility for maintenance and distribution of mutant mice was initially placed on individual investigators, which was a tremendous burden in terms of cost, labor and space. In 1999, the NIH recognized the need for a resource to protect the investment in mutant mouse strains and ensure open access to all biomedical researchers and established the Mutant Mouse Regional Resource Centers (MMRRC). Since 1999, the central goal of the MMRRC-UNC has been to work collectively with MMRRC consortium partners to develop and maintain high standards for importation, rederivation, cryopreservation, and distribution of mutant mouse strains to biomedical investigators. The MMRRC- UNC will continue to contribute to the goals of the Consortium in the next project period by implementing the following Specific Aims devoted to continuing its successful role as a cryoarchive and distribution center and incorporating research goals that synergize with and extend the value of the resource: 1) Streamline and improve operating procedures to increase importation, distribution, and cryoarchive of mouse strains. 2) Establish, maintain, and distribute a comprehensive cryoarchive for the Collaborative Cross (CC) resource. 3) Develop and disseminate computational tools for mouse genetic QC and genomics research, which will enhance phenotypic reproducibility. 4) Investigate the interaction of genetics and environment on experimental variability and reproducibility. !
Genetically engineered mouse models provide a tractable system for studying human development and disease, fueling discoveries that can dramatically improve public health. The MMRRC-UNC imports, archives and distributes mouse strains to the scientific community to protect and provide efficient access to this valuable resource. In addition, the MMRRC-UNC has developed synergistic research projects to support rigor and reproducibility of biomedical research using mouse models.
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| Terajima, Hideki; Yoshitane, Hikari; Yoshikawa, Tomoko et al. (2018) A-to-I RNA editing enzyme ADAR2 regulates light-induced circadian phase-shift. Sci Rep 8:14848 |
| Morgan, Andrew P; Pardo-Manuel de Villena, Fernando (2017) Sequence and Structural Diversity of Mouse Y Chromosomes. Mol Biol Evol 34:3186-3204 |
| Wagner, Gregory R; Bhatt, Dhaval P; O'Connell, Thomas M et al. (2017) A Class of Reactive Acyl-CoA Species Reveals the Non-enzymatic Origins of Protein Acylation. Cell Metab 25:823-837.e8 |
| Mu, Weipeng; Starmer, Joshua; Shibata, Yoichiro et al. (2017) EZH1 in germ cells safeguards the function of PRC2 during spermatogenesis. Dev Biol 424:198-207 |
| Srivastava, Anuj; Morgan, Andrew P; Najarian, Maya L et al. (2017) Genomes of the Mouse Collaborative Cross. Genetics 206:537-556 |
| Morgan, Andrew P; Fu, Chen-Ping; Kao, Chia-Yu et al. (2015) The Mouse Universal Genotyping Array: From Substrains to Subspecies. G3 (Bethesda) 6:263-79 |
| Morgan, Andrew P (2015) argyle: An R Package for Analysis of Illumina Genotyping Arrays. G3 (Bethesda) 6:281-6 |
| Lloyd, Kent; Franklin, Craig; Lutz, Cat et al. (2015) Reproducibility: use mouse biobanks or lose them. Nature 522:151-3 |
| Fedoriw, Andrew M; Menon, Debashish; Kim, Yuna et al. (2015) Key mediators of somatic ATR signaling localize to unpaired chromosomes in spermatocytes. Development 142:2972-80 |
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