This application for an NIDDK Biotechnology Center represents a natural confluence of several strong research communities at the University of Washington. This proposal brings together an already established I gene microarray facility under the direction of Dr. Roger Bumgarner, with investigators at the cutting edge of research in the areas of initiation of diabetes and its complications, control of the immune response, regulation of cell proliferation, cell hypertrophy, and cell migration in renal injury, hepatocyte regeneration after injury, intestinal development, and hematopoietic stem cell biology. An overriding aim of this center is to develop a working gene chip containing all of the known sequence verified genes of the mouse genome, which can be utilized by investigators in the above areas. We anticipate this approach will particularly benefit investigators utilizing marine systems bearing transgenes, genetic deletions, or controllable genetic mutations in purified cell populations or specific organ systems to study mechanisms of disease. We concurrently seek to develop stringent approaches to data generation and analysis that will increase the amount and establish the validity of the information that will be obtained as the result of application of gene array approaches to our disease models. This will be accomplished through the following four specific aims: 1 ) Expand the collection of clones available for construction of arrays by acquiring Unigene sets of mouse cDNA clones and additional human cDNA clones; 2) Increase the throughput and data storage capacity of the array facility; 3) Implement and integrate our data analysis with an expression database; 4) Test and implement protocols for RNA and signal amplification.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
5U24DK058813-03
Application #
6635331
Study Section
Special Emphasis Panel (ZDK1-GRB-B (M1))
Program Officer
Star, Robert A
Project Start
2001-06-25
Project End
2004-05-31
Budget Start
2003-06-01
Budget End
2004-05-31
Support Year
3
Fiscal Year
2003
Total Cost
$492,500
Indirect Cost
Name
University of Washington
Department
Pathology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Wessells, Hunter; Sullivan, Chris J; Tsubota, Yoshiaki et al. (2009) Transcriptional profiling of human cavernosal endothelial cells reveals distinctive cell adhesion phenotype and role for claudin 11 in vascular barrier function. Physiol Genomics 39:100-8
Kharasch, Evan D; Schroeder, Jesara L; Bammler, Theo et al. (2006) Gene expression profiling of nephrotoxicity from the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (""compound A"") in rats. Toxicol Sci 90:419-31
Sullivan, Chris J; Teal, Thomas H; Luttrell, Ian P et al. (2005) Microarray analysis reveals novel gene expression changes associated with erectile dysfunction in diabetic rats. Physiol Genomics 23:192-205
Yeung, Ka Yee; Medvedovic, Mario; Bumgarner, Roger E (2004) From co-expression to co-regulation: how many microarray experiments do we need? Genome Biol 5:R48
Medvedovic, M; Yeung, K Y; Bumgarner, R E (2004) Bayesian mixture model based clustering of replicated microarray data. Bioinformatics 20:1222-32
Vanasse, Gary J; Winn, Robert K; Rodov, Sofya et al. (2004) Bcl-2 overexpression leads to increases in suppressor of cytokine signaling-3 expression in B cells and de novo follicular lymphoma. Mol Cancer Res 2:620-31
Wei, Caimiao; Li, Jiangning; Bumgarner, Roger E (2004) Sample size for detecting differentially expressed genes in microarray experiments. BMC Genomics 5:87
Yeung, Ka Yee; Medvedovic, Mario; Bumgarner, Roger E (2003) Clustering gene-expression data with repeated measurements. Genome Biol 4:R34
Yeung, Ka Yee; Bumgarner, Roger E (2003) Multiclass classification of microarray data with repeated measurements: application to cancer. Genome Biol 4:R83