The mission of the Genomics Shared Resource is to support Cancer Center members in their studies of DNA as well as gene expression. The Genomics Shared Resource is composed of two facilities. These are DNA Analysis, providing DNA sequencing and mouse genotyping service, and Microarray/Q-PCR, providing lllumina-based microarray analysis, as well as full-service real-time quantitative PCR. DNA Analysis: Full-service DNA sequence analvsis is provided using a 16 capillary-based instrument. PCR-based mouse genotyping is performed to characterize transgenic mice. Cancer Center investigators will soon also be provided access to next-gen sequencing, which will enable quantitative unbiased expression profiling, analysis of RNA splicing, chip-seq determining genomic targets for transcription factors, and identifying cancer-associated mutations. For mouse qenotvpinq. tail samples are delivered directly from Animal Resources to DNA Analysis. DNA is isolated and analyzed using an investigatordeveloped PCR assay followed by agarose gel analysis. Results are rapidly returned to investigators, speeding selection of desired transgenic mice, accelerating research and reducing mouse costs. Microarray/Q-PCR: Global gene expression analysis is performed using the Illumina BeadStation microarray system. Such microarray analvsis for human, mouse and rat samples is both robust and cost effective. This full-service analysis starts with investigator RNA, and returns initially analyzed data to them. Extensive additional microarray data analysis to put results in a statistical, biological, or pathway context is available from the IDM Shared Resource. Recently, global profiling of miRNAs has been introduced, and ongoing enhancements are being made in microarray analysis. Full service Q-PCR is also provided, where investigators can provide RNA and have the facility design primers and an experimental plan, ultimately retuning fold-difference data. Shared Resource staff also provide traininq on a suite of common-use instrumentation, including a multifunctional fluorescence scanner and phosphorlmager, cooled CCD blot/gel imager, near-IR (LI-COR) scanners, microplate luminometer, and Nanodrop Spectrophotometer. The Genomics Shared Resource is broadly used, having supported over 250 publications in the last funding period. In the past year, 41 Cancer Center members, representing all 4 Programs, utilized the services of the facility. Overall, $121,554 in CCSG support is requested in the first year, representing 16.4% of the total projected operating budget for the Genomics Shared Resource.

Public Health Relevance

Mutations in genes and changes in gene expression are critical events in the transition from normal cell behavior to tumor progression. The Genomics Shared Resource supports this analysis by Cancer Center investigators, from the level of single genes, to global changes in gene expression.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA030199-32
Application #
8473824
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
32
Fiscal Year
2013
Total Cost
$204,911
Indirect Cost
$100,414
Name
Sanford-Burnham Medical Research Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Wei, Yang; Toth, Julia I; Blanco, Gabrielle A et al. (2018) Adapted ATPase domain communication overcomes the cytotoxicity of p97 inhibitors. J Biol Chem 293:20169-20180
Tinoco, Roberto; Carrette, Florent; Henriquez, Monique L et al. (2018) Fucosyltransferase Induction during Influenza Virus Infection Is Required for the Generation of Functional Memory CD4+ T Cells. J Immunol 200:2690-2702
Wonder, Emily; Simón-Gracia, Lorena; Scodeller, Pablo et al. (2018) Competition of charge-mediated and specific binding by peptide-tagged cationic liposome-DNA nanoparticles in vitro and in vivo. Biomaterials 166:52-63
Limpert, Allison S; Lambert, Lester J; Bakas, Nicole A et al. (2018) Autophagy in Cancer: Regulation by Small Molecules. Trends Pharmacol Sci 39:1021-1032
Fujita, Yu; Khateb, Ali; Li, Yan et al. (2018) Regulation of S100A8 Stability by RNF5 in Intestinal Epithelial Cells Determines Intestinal Inflammation and Severity of Colitis. Cell Rep 24:3296-3311.e6
Scully, Kathleen M; Lahmy, Reyhaneh; Signaevskaia, Lia et al. (2018) E47 Governs the MYC-CDKN1B/p27KIP1-RB Network to Growth Arrest PDA Cells Independent of CDKN2A/p16INK4A and Wild-Type p53. Cell Mol Gastroenterol Hepatol 6:181-198
Borlido, Joana; Sakuma, Stephen; Raices, Marcela et al. (2018) Nuclear pore complex-mediated modulation of TCR signaling is required for naïve CD4+ T cell homeostasis. Nat Immunol 19:594-605
Follis, Ariele Viacava; Llambi, Fabien; Kalkavan, Halime et al. (2018) Regulation of apoptosis by an intrinsically disordered region of Bcl-xL. Nat Chem Biol 14:458-465
Pathria, Gaurav; Scott, David A; Feng, Yongmei et al. (2018) Targeting the Warburg effect via LDHA inhibition engages ATF4 signaling for cancer cell survival. EMBO J 37:
Sun, Younguk; Chen, Bo-Rui; Deshpande, Aniruddha (2018) Epigenetic Regulators in the Development, Maintenance, and Therapeutic Targeting of Acute Myeloid Leukemia. Front Oncol 8:41

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