Comprehensive Cancer Center (UNC LCCC) and the UNC Program in Biotechnology and Molecular Biology (PMBB). The objective of the facility is to provide genetically modified mice and supporting technologies to UNC researchers at a reasonable cost and to support the Cancer Center's strategic emphasis on mouse models of human disease. The long-term goal is to build a state-of-the-art facility that provides a wide array of gene expression and deletion strategies. Experimental manipulation of the mouse has become a powerful tool for the study of cancer mechanisms and for the generation of many human disease models. Given widespread cell specificity, physiological complexities, and the dynamic nature of cancer development, animal models can be essential reagents in etiologic, prevention and treatment research. The objectives of this facility are to: Advise investigators in the design and follow-up of animal experiments, Generate genetically modified cells and animals for individual research programs, Provide basic support technologies (e.g., gamete and embryo cryopreservation), Use and develop new reagents and technologies (e.g., nuclear transfer), Decrease cost by centralizing functions such as genotyping. The Core is led by Drs. Terry Van Dyke (Faculty Director) and Randy Thresher (Facility Director). The Core adds value to the Center by providing highly skilled services at reasonable costs. Highlights of research supported by the Core include the production of glioblastoma and breast cancer models. The Core supports a new function, mouse genotyping, for: i) routine and timely genotyping to improve colony management; ii) marker-assisted generation of""""""""speed congenics""""""""; and iii) high throughput genome scans to help identify modified genes. Future plans for the Core include ICSI and cloning, lentivirus-based transgenics, high throughput vector construction, new ES cell line derivation and the production of strain 129-based Cre expressing lines.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016086-33
Application #
7645554
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2007-12-01
Budget End
2008-11-30
Support Year
33
Fiscal Year
2008
Total Cost
$382,996
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Shen, Hui; Shih, Juliann; Hollern, Daniel P et al. (2018) Integrated Molecular Characterization of Testicular Germ Cell Tumors. Cell Rep 23:3392-3406
Shao, Wenwei; Chen, Xiaojing; Samulski, Richard J et al. (2018) Inhibition of antigen presentation during AAV gene therapy using virus peptides. Hum Mol Genet 27:601-613
Gao, Yanzhe; Kardos, Jordan; Yang, Yang et al. (2018) The Cancer/Testes (CT) Antigen HORMAD1 promotes Homologous Recombinational DNA Repair and Radioresistance in Lung adenocarcinoma cells. Sci Rep 8:15304
Schaefer, Kristina N; Bonello, Teresa T; Zhang, Shiping et al. (2018) Supramolecular assembly of the beta-catenin destruction complex and the effect of Wnt signaling on its localization, molecular size, and activity in vivo. PLoS Genet 14:e1007339
Zuze, Takondwa; Painschab, Matthew S; Seguin, Ryan et al. (2018) Plasmablastic lymphoma in Malawi. Infect Agent Cancer 13:22
Wang, Jeremy R; Holt, James; McMillan, Leonard et al. (2018) FMLRC: Hybrid long read error correction using an FM-index. BMC Bioinformatics 19:50
Lee, Janie M; Abraham, Linn; Lam, Diana L et al. (2018) Cumulative Risk Distribution for Interval Invasive Second Breast Cancers After Negative Surveillance Mammography. J Clin Oncol 36:2070-2077
Thomas, Nancy E; Edmiston, Sharon N; Orlow, Irene et al. (2018) Inherited Genetic Variants Associated with Melanoma BRAF/NRAS Subtypes. J Invest Dermatol 138:2398-2404
Cousins, Emily M; Goldfarb, Dennis; Yan, Feng et al. (2018) Competitive Kinase Enrichment Proteomics Reveals that Abemaciclib Inhibits GSK3? and Activates WNT Signaling. Mol Cancer Res 16:333-344
Armstrong, Robin L; Penke, Taylor J R; Strahl, Brian D et al. (2018) Chromatin conformation and transcriptional activity are permissive regulators of DNA replication initiation in Drosophila. Genome Res 28:1688-1700

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