State the application's broad, long-term objectives and specific aims, making reference to the health relatedness of the project. Describe concisely the researchdesign and methods for achievingthese goals. Avoid summaries of past accomplishments and the use of the first person. This abstract is meant to serve as a succinct and accurate descriptionof the proposed work when separated from the application. If the application is funded, this description, as is, will become public information. Therefore, do not include proprietary/confidentialinformation. DO NOT EXCEED THE SPACE PROVIDED. Due to the recent completion of the human and mouse genomes as well as advances in mouse technologies, there has been an enormous increase in the number of mouse mutants and models for human disease. Maintaining and distributing pathogen-free mouse strains is both labor-intensive and costly for individual investigators to sustain longterm. The NIH/NCRR recognized the need for a common repository and distribution center for genetically modified mice, and in 1999 they responded by funding the Mutant Mouse Regional Resource Centers (MMRRC). UNC-Chapel Hill is one of four MMRRC centers that are developing this resource for the benefit of the entire .biomedical community. Since the initial funding in 1999, a significant amount of effort has been invested in creating the organizational infrastructure and establishing standard operating procedures (SOPs) for importation, rederivation, phenotyping, cryopreservation and distribution of mutant mouse strains. In 2001, the MMRRC-UNC accepted its first strain and has experienced significant-expansionever since. In parallel with these efforts, the MMRRC has also taken advantage of the expertise available at UNC to bring new technologies and resources to the community such as mutant ES-cell lines, gnotobiotic strains and improved in vitro fertilization methods. To meet future demands for MMRRC services and improve upon existing technologies, this proposal aims to: (1) import, archive and distribute genetically modified mouse strains, (2) increase visibility of the MMRRC through advertising and solicitations targeting the biomedical research community, (3) develop improved and reliable methods for assisted fertilization, (4) integrate gnotobiotic strain development into MMRRC services (5) generate an allelic series of point mutations in genes of interest as a community resource. PERFORMANCE SITE(S) (organization, city, state) University of North Carolina, Chapel Hill, NC KEY PERSONNEL. See instructions. Use continuation pages as needed to provide the required information in the format shown below. Start with Principal Investigator. List all other key personnel in alphabetical order, last name first. [Name [Organization . |Role on Project Magnuson, Terry University of North Carolina, Chapel Hill Principal Investigator Godfrey, Virginia University of North Carolina, Chapel Hill Investigator - histopathology and phenotyping Mohr, Kathleen University of North Carolina, Chapel Hill Facility Technical Director Disclosure Permission Statement. Applicable to SBIR/STTROnly. See instructions. HHYes LZl No PHS 398 (Rev.05/01) Page 2 Number pages consecutively at thebottom throughout Form Page 2 the application. Do not use suffixes such as 2a, 2b. Principal Investigator/Program Director (Last, First, Middle): MagnUSO!""""""""), Terry The name of the principal investigator/programdirector must be provided at the top of each printed page and each continuation page. RESEARCH GRANT
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| Shpargel, Karl B; Sengoku, Toru; Yokoyama, Shigeyuki et al. (2012) UTX and UTY demonstrate histone demethylase-independent function in mouse embryonic development. PLoS Genet 8:e1002964 |
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| Castillo, Andrew; Morse 3rd, Herbert C; Godfrey, Virginia L et al. (2007) Overexpression of Eg5 causes genomic instability and tumor formation in mice. Cancer Res 67:10138-47 |
