The Computational and Functional Genomics Core will serve all projects, assisting the investigators in research design and data processing and management, as well as in all technical aspects of microarray experiments. A major activity will consist of designing and processing the results of cDNA, oligonucleotide, protein and antibody array experiments by which to analyze alteration of gene expression, protein abundance and protein-protein interaction within specimens of mice exposed to hypoxia or hypercapnia.
The Specific Aims of this Core facility are as follows: 1) To provide consultation, training and technical and bioinformatic assistance in all aspects of genomic studies, from experimental design and RNA and protein hybridization with the arrays to quality control, data processing and management. 2) To assist the projects to deposit their microarray data in the GEO database of NCBI, to organize and maintain transcriptomic and proteomic dbases of hypoxia effects in wildtype and in genetically modified mice to probe specific mechanisms for adaptation or injury and include these databases into the website of the Program Project after publication in peer-reviewed journals. 3) To provide consultation and training in the use of advanced statistical methods and mathematical modeling and to assist investigators in research design, data processing and management.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD032573-14
Application #
7659698
Study Section
Special Emphasis Panel (ZHD1)
Project Start
2008-08-01
Project End
2010-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
14
Fiscal Year
2008
Total Cost
$51,688
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Azad, Priti; Zhao, Huiwen W; Cabrales, Pedro J et al. (2016) Senp1 drives hypoxia-induced polycythemia via GATA1 and Bcl-xL in subjects with Monge's disease. J Exp Med 213:2729-2744
Yao, Hang; Azad, Priti; Zhao, Huiwen W et al. (2016) The Na+/HCO3- co-transporter is protective during ischemia in astrocytes. Neuroscience 339:329-337
Jha, Aashish R; Zhou, Dan; Brown, Christopher D et al. (2016) Shared Genetic Signals of Hypoxia Adaptation in Drosophila and in High-Altitude Human Populations. Mol Biol Evol 33:501-17
Pamenter, Matthew E; Haddad, Gabriel G (2015) High-throughput cell death assays. Methods Mol Biol 1254:153-63
Salameh, Ahlam Ibrahim; Ruffin, Vernon A; Boron, Walter F (2014) Effects of metabolic acidosis on intracellular pH responses in multiple cell types. Am J Physiol Regul Integr Comp Physiol 307:R1413-27
Gu, Xiang Q; Pamenter, Matthew E; Siemen, Detlef et al. (2014) Mitochondrial but not plasmalemmal BK channels are hypoxia-sensitive in human glioma. Glia 62:504-13
Gersten, Merril; Zhou, Dan; Azad, Priti et al. (2014) Wnt pathway activation increases hypoxia tolerance during development. PLoS One 9:e103292
Udpa, Nitin; Ronen, Roy; Zhou, Dan et al. (2014) Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. Genome Biol 15:R36
Douglas, Robert M; Chen, Alice H; Iniguez, Alejandra et al. (2013) Chemokine receptor-like 2 is involved in ischemic brain injury. J Exp Stroke Transl Med 6:1-6
Parker, Mark D; Boron, Walter F (2013) The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters. Physiol Rev 93:803-959

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