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.
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.
|Lechtenberg, Bernhard C; Rajput, Akhil; Sanishvili, Ruslan et al. (2016) Structure of a HOIP/E2~ubiquitin complex reveals RBR E3 ligase mechanism and regulation. Nature 529:546-50|
|Zhong, Zhenyu; Umemura, Atsushi; Sanchez-Lopez, Elsa et al. (2016) NF-ÎºB Restricts Inflammasome Activation via Elimination of Damaged Mitochondria. Cell 164:896-910|
|Olson, Erika J; Lechtenberg, Bernhard C; Zhao, Chunxia et al. (2016) Modifications of a Nanomolar Cyclic Peptide Antagonist for the EphA4 Receptor To Achieve High Plasma Stability. ACS Med Chem Lett 7:841-6|
|Tinoco, Roberto; Carrette, Florent; Barraza, Monique L et al. (2016) PSGL-1 Is an Immune Checkpoint Regulator that Promotes T Cell Exhaustion. Immunity 44:1190-203|
|Zhao, Wei; Mazar, Joseph; Lee, Bongyong et al. (2016) The Long Noncoding RNA SPRIGHTLY Regulates Cell Proliferation in Primary Human Melanocytes. J Invest Dermatol 136:819-28|
|Singec, Ilyas; Crain, Andrew M; Hou, Junjie et al. (2016) Quantitative Analysis of Human Pluripotency and Neural Specification by In-Depth (Phospho)Proteomic Profiling. Stem Cell Reports 7:527-42|
|McQuary, Philip R; Liao, Chen-Yu; Chang, Jessica T et al. (2016) C.Â elegans S6K Mutants Require a Creatine-Kinase-like Effector for Lifespan Extension. Cell Rep 14:2059-67|
|Moscat, Jorge; Karin, Michael; Diaz-Meco, Maria T (2016) p62 in Cancer: Signaling Adaptor Beyond Autophagy. Cell 167:606-609|
|Miletic, Ana V; Jellusova, Julia; Cato, Matthew H et al. (2016) Essential Role for Survivin in the Proliferative Expansion of Progenitor and Mature B Cells. J Immunol 196:2195-204|
|Koh, Mei Yee; Gagea, Mihai; Sargis, Timothy et al. (2016) A new HIF-1Î±/RANTES-driven pathway to hepatocellular carcinoma mediated by germline haploinsufficiency of SART1/HAF in mice. Hepatology 63:1576-91|
Showing the most recent 10 out of 425 publications