A large scale effort to identify polymorphisms involved in environmentally induced disease, known as the Environmental Genome Project (EGP), was initiated at NIEHS in 1998. The EGP further aims to characterize health effects of polymorphisms, and to conduct epidemiologic studies of gene-environment interactions. The Molecular Genetics Core Facility infrastructure was created to perform nucleic acid sample isolation, sample management and genetics studies to support this and other genetics efforts at NIEHS. During the past fiscal year, robotic automation was expanded to increase throughput, reduce manual labor, and decrease the cost of genetic studies performed at NIEHS. We developed a dynamic web portal to manage the core facility, and an associated database to track both work product and cost of each study. We established gene resequencing infrastructure which provides support from primer design through data analysis, while reducing cost per reaction. We also developed an automated and gel-free mouse tail genotyping method to reduce labor and expense of this time consuming and costly aspect of maintaining mouse colonies for genetic studies. Both the methods automation and methods development aspects of our workgroup offer opportunities for accelerated development of new therapies for prevention of environmentally induced disease.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2009
Total Cost
$1,629,408
Indirect Cost
City
State
Country
Zip Code
Hoopes, Samantha L; Gruzdev, Artiom; Edin, Matthew L et al. (2017) Generation and characterization of epoxide hydrolase 3 (EPHX3)-deficient mice. PLoS One 12:e0175348
House, John S; Nichols, Cody E; Li, Huiling et al. (2017) Vagal innervation is required for pulmonary function phenotype in Htr4(-/-) mice. Am J Physiol Lung Cell Mol Physiol 312:L520-L530
Lai, Lihua; Azzam, Kathleen M; Lin, Wan-Chi et al. (2016) MicroRNA-33 Regulates the Innate Immune Response via ATP Binding Cassette Transporter-mediated Remodeling of Membrane Microdomains. J Biol Chem 291:19651-60
Cheng, Jennifer; Dackor, Ryan T; Bradbury, J Alyce et al. (2016) Contribution of alveolar type II cell-derived cyclooxygenase-2 to basal airway function, lung inflammation, and lung fibrosis. FASEB J 30:160-73
Davis, Felicity M; Goulding, Eugenia H; D'Agostin, Diane M et al. (2016) Male infertility in mice lacking the store-operated Ca(2+) channel Orai1. Cell Calcium 59:189-97
Steinckwich, Natacha; Myers, Page; Janardhan, Kyathanahalli S et al. (2015) Role of the store-operated calcium entry protein, STIM1, in neutrophil chemotaxis and infiltration into a murine model of psoriasis-inflamed skin. FASEB J 29:3003-13
Gowdy, K M; Madenspacher, J H; Azzam, K M et al. (2015) Key role for scavenger receptor B-I in the integrative physiology of host defense during bacterial pneumonia. Mucosal Immunol 8:559-71
Van, Christopher; Williams, Jessica S; Kunkel, Thomas A et al. (2015) Deposition of histone H2A.Z by the SWR-C remodeling enzyme prevents genome instability. DNA Repair (Amst) 25:9-14
Clement, Tracy M; Inselman, Amy L; Goulding, Eugenia H et al. (2015) Disrupting Cyclin Dependent Kinase 1 in Spermatocytes Causes Late Meiotic Arrest and Infertility in Mice. Biol Reprod 93:137
Hsia, B J; Whitehead, G S; Thomas, S Y et al. (2015) Trif-dependent induction of Th17 immunity by lung dendritic cells. Mucosal Immunol 8:186-97

Showing the most recent 10 out of 63 publications