The Cancer Model Development Resource (CMDR) at JAX is a component of Genetic Resource Science (GRS), a group of over 100 people with broad expertise in mouse genetics and molecular biology necessary to manipulate the mouse genome. Dr. Leah Rae Donahue, Director of Genetic Resource Sciences, and Dr. Leonard Shultz, Professor, co-lead the CMDR. The CMDR provides JAX Cancer Center (JAXCC) investigators access to existing cancer models and supports development of new mouse models tailored to specific cancer research questions of importance to the Cancer Center. In turn, these models are made available to the JAXCC and wider scientific community through the GRS Repository. The CMDR provides JAXCC investigators access to mouse strains, the expertise of scientists in the Genetic Resource Science program, and project management. The GRS Repository is the largest single collection of genetically defined mouse strains anywhere in the world, and maintains an enormous variety of live strains (~1,600 at any given time), while other strains are maintained as cryopreserved stocks. To encourage use of the live resource, JAXCC members are supplied with mice free of charge, either as breeding pairs, small numbers of mutants and controls from mutant strains, or individual mice from strain panels. Additionally, the CMDR provides project management and genetic expertise to facilitate the development of cancer models by xenografts of human cancer samples into the NSG (NOD.Cg-Prkdcscid II2rgtm1Wji/Szj) mouse developed by Dr. Shultz. The CMDR advises JAXCC members who wish to develop specialized host strains tailored for particular scientific questions. Models are also developed for other research applications by combining mutant alleles to make compound mutant stocks. The CMDR and coordinates the model development process, working with the Genetic Engineering Technologies and Phenotyping Technologies resources as needed. The CMDR project manager coordinates animal care, management of biological materials, and surgical services to facilitate model development. The long-term objective is assist JAXCC members in their research by enabling the use of the full suite of genetic manipulation techniques and mouse model development.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA034196-32
Application #
9298409
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
32
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
Gong, Liang; Wong, Chee-Hong; Cheng, Wei-Chung et al. (2018) Picky comprehensively detects high-resolution structural variants in nanopore long reads. Nat Methods 15:455-460
Noorbakhsh, Javad; Kim, Hyunsoo; Namburi, Sandeep et al. (2018) Distribution-based measures of tumor heterogeneity are sensitive to mutation calling and lack strong clinical predictive power. Sci Rep 8:11445
Gatti, D M; Weber, S N; Goodwin, N C et al. (2018) Genetic background influences susceptibility to chemotherapy-induced hematotoxicity. Pharmacogenomics J 18:319-330
deCarvalho, Ana C; Kim, Hoon; Poisson, Laila M et al. (2018) Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma. Nat Genet 50:708-717
Mistri, Tapan Kumar; Arindrarto, Wibowo; Ng, Wei Ping et al. (2018) Dynamic changes in Sox2 spatio-temporal expression promote the second cell fate decision through Fgf4/Fgfr2 signaling in preimplantation mouse embryos. Biochem J 475:1075-1089
Leidy-Davis, Tiffany; Cheng, Kai; Goodwin, Leslie O et al. (2018) Viable Mice with Extensive Gene Humanization (25-kbp) Created Using Embryonic Stem Cell/Blastocyst and CRISPR/Zygote Injection Approaches. Sci Rep 8:15028
Raghupathy, Narayanan; Choi, Kwangbom; Vincent, Matthew J et al. (2018) Hierarchical analysis of RNA-seq reads improves the accuracy of allele-specific expression. Bioinformatics 34:2177-2184
Presa, Maximiliano; Racine, Jeremy J; Dwyer, Jennifer R et al. (2018) A Hypermorphic Nfkbid Allele Contributes to Impaired Thymic Deletion of Autoreactive Diabetogenic CD8+ T Cells in NOD Mice. J Immunol 201:1907-1917
Pullagura, Sri Ramulu N; Buaas, Bill; Gray, Nichelle et al. (2018) Functional Redundancy of DICER Cofactors TARBP2 and PRKRA During Murine Embryogenesis Does Not Involve miRNA Biogenesis. Genetics 208:1513-1522
Cho, Sung-Yup; Sung, Chang Ohk; Chae, Jeesoo et al. (2018) Alterations in the Rho pathway contribute to Epstein-Barr virus-induced lymphomagenesis in immunosuppressed environments. Blood 131:1931-1941

Showing the most recent 10 out of 1156 publications