This core will provide expertise in the production and use of cDNA and oligonucleotide microarrays and the bioinformatics support required for data storage and analysis. The investigator provides the core laboratory with a minimum of 1 microgram of total RNA from control and test cell samples; core personnel produce the target RNA, the microarrays, the hybridization, the image analysis, and preliminary data analysis. cDNA arrays are produced by printing PCR products from IMAGE consortium cDNA clones onto glass microscope slides using a commercial 3-axis robotic array similar to the Stanford design. Target total RNA (1 microgram) is prepared by RT-PCR using Oligo-dT and random primers in the presence of Aminoallyl-dUTP. The cDNA is dye-labeled by coupling NHS-ester Cys3 or Cy5 dyes to free amines. The labeled cDNA is hybridized to the microarray in slide chambers or in a GeneTAC hybridization workstation and scanned using a scanning laser confocal microscope (SanArray 5000, GSI Luminics, Inc.). The image data files are analyzed using IPlab (Scanalytics, Inc.) And the resulting data transferred to ArrayDB (NHGIR, Oracle version x.y). Investigators retrieve the DNA clones, 9,200 human clones, and approximately 21,000 human ESTs. We are currently producing arrays with approximately 3,600 features/slide. Additional clones and higher density arrays will be produced as they become available and as our expertise increases. The core also has the complete complement of Affymetrix instrumentation and bioinformatics tools available and currently has human """"""""HuGeneFL"""""""", mouse """"""""Mu11K"""""""", and human """"""""Cancer G110"""""""" GeneChips in stock for immediate use. Finally, the core also has access to significant bioinformatics resources in terms of computational hardware, expertise, and software/database resources. This element of the laboratory is critical to the successful use and evaluation of DNA microarray experiments.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA071907-07
Application #
6595015
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2002-06-01
Project End
2003-05-31
Budget Start
Budget End
Support Year
7
Fiscal Year
2002
Total Cost
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Dumitrache, Lavinia C; McKinnon, Peter J (2017) Polynucleotide kinase-phosphatase (PNKP) mutations and neurologic disease. Mech Ageing Dev 161:121-129
Ribeiro, Raul C; Antillon, Federico; Pedrosa, Francisco et al. (2016) Global Pediatric Oncology: Lessons From Partnerships Between High-Income Countries and Low- to Mid-Income Countries. J Clin Oncol 34:53-61
Doherty, Joanne R; Nilsson, Lisa M; Kuliyev, Emin et al. (2014) Embryonic Expression and Function of the Xenopus Ink4d Cyclin D-Dependent Kinase Inhibitor. Cell Dev Biol 3:
Morfouace, Marie; Shelat, Anang; Jacus, Megan et al. (2014) Pemetrexed and gemcitabine as combination therapy for the treatment of Group3 medulloblastoma. Cancer Cell 25:516-29
Wang, Yuefeng; Fisher, John C; Mathew, Rose et al. (2011) Intrinsic disorder mediates the diverse regulatory functions of the Cdk inhibitor p21. Nat Chem Biol 7:214-21
Trikha, Prashant; Sharma, Nidhi; Opavsky, Rene et al. (2011) E2f1-3 are critical for myeloid development. J Biol Chem 286:4783-95
Doghman, Mabrouka; El Wakil, Abeer; Cardinaud, Bruno et al. (2010) Regulation of insulin-like growth factor-mammalian target of rapamycin signaling by microRNA in childhood adrenocortical tumors. Cancer Res 70:4666-75
Pottier, N; Paugh, S W; Ding, C et al. (2010) Promoter polymorphisms in the ?-2 adrenergic receptor are associated with drug-induced gene expression changes and response in acute lymphoblastic leukemia. Clin Pharmacol Ther 88:854-61
Huang, Danny T; Ayrault, Olivier; Hunt, Harold W et al. (2009) E2-RING expansion of the NEDD8 cascade confers specificity to cullin modification. Mol Cell 33:483-95
Forget, Antoine; Ayrault, Olivier; den Besten, Willem et al. (2008) Differential post-transcriptional regulation of two Ink4 proteins, p18 Ink4c and p19 Ink4d. Cell Cycle 7:3737-46

Showing the most recent 10 out of 124 publications