A new Center on Environmental Genetics is proposed by the University of Cincinnati. The focus of this Center will be to investigate the impact of genetic diversity on the response of the individual, or populations, to toxic environmental agents. The Center will include a multidisciplinary approach, from """"""""the molecule to the human,"""""""" devoted to application of molecular biology and genetics to environmental research. The fundamental strategy of the Center is to understand variation in response to toxic agents due to the underlying interindividual differences in genetic predisposition. Basic research may include everything from microbes and lower eukaryotes to mammals and human material. Center research will take advantage of the usefulness of genetic variants, i.e. genetically different subpopulations, resistant versus sensitive groups, and/or interindividual and intraspecies differences. It is clear that interindividual genetic differences can lead to dramatic dissimilarities in the response to a wide variety of environmental substances. An appreciation of these differences, and an understanding of the underlying mechanisms, are critical in the evaluation of risk of adverse health effects caused by toxic environmental agents. Individual variation often reflects allelic differences in genes encoding proteins involved in critical life functions such as receptors, drug metabolism, ion channels, multidrug resistance glycoprotein pumps, second-messenger pathways, DNA repair, and chelation of metals. The elucidation of these functions that can influence interindividual response to toxic agents, and the evaluation of their genetic diversity in the population, will be the central focus of the Center. The identification of these underlying causes of genetic differences in response to toxic agents is an important key to understanding the basic mechanisms of toxicity and provides the basis for both preventing adverse health effects and exploring opportunities for interventions in the disease process. The four Research Cores of the new Center represent existing strengths and interactions among scientists within the University of Cincinnati Medical Center that are relevant to genetics. The central focus of the Ecogenetics Research Core is the identification and characterization of genetic polymorphisms that affect the metabolism, and therefore the toxicity, of foreign chemicals. The other Research Cores--Reproductive & Developmental Toxicology, Genetic Toxicology, and Oxidative Stress Toxicology--are focused on three specific areas of toxicology of major importance. These Research Cores investigate specific toxic effects of environmental agents with an emphasis on the use of genetic techniques. The role of environmental substances in causing infertility, in utero toxicity, and birth defects is an important public health issue. The impact of environmental agents on the structure of genetic material itself, leading to mutations and cancer, is an area of vital importance. Oxidative stress is an emerging area of importance which may underlie many diverse toxic effects of environmental agents in biological systems. This new Center will be unique among NIEHS Centers and will provide. an important. resource to the environmental research community.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES006096-02
Application #
3102383
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
1992-06-15
Project End
1997-03-31
Budget Start
1993-04-01
Budget End
1994-03-31
Support Year
2
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Cincinnati
Department
Type
Schools of Medicine
DUNS #
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Bermúdez, Mei-Ling; Skelton, Matthew R; Genter, Mary Beth (2018) Intranasal carnosine attenuates transcriptomic alterations and improves mitochondrial function in the Thy1-aSyn mouse model of Parkinson's disease. Mol Genet Metab 125:305-313
Reigle, Beverly S; Zhang, Bin (2018) Women's Rehabilitation Experiences Following Breast Cancer Surgery. Rehabil Nurs 43:195-200
Whitt, Jordan; Woo, Vivienne; Lee, Patrick et al. (2018) Disruption of Epithelial HDAC3 in Intestine Prevents Diet-Induced Obesity in Mice. Gastroenterology 155:501-513
Uno, Shigeyuki; Nebert, Daniel W; Makishima, Makoto (2018) Cytochrome P450 1A1 (CYP1A1) protects against nonalcoholic fatty liver disease caused by Western diet containing benzo[a]pyrene in mice. Food Chem Toxicol 113:73-82
Vuong, Ann M; Yolton, Kimberly; Poston, Kendra L et al. (2018) Childhood polybrominated diphenyl ether (PBDE) exposure and executive function in children in the HOME Study. Int J Hyg Environ Health 221:87-94
Lee, Alison G; Le Grand, Blake; Hsu, Hsiao-Hsien Leon et al. (2018) Prenatal fine particulate exposure associated with reduced childhood lung function and nasal epithelia GSTP1 hypermethylation: Sex-specific effects. Respir Res 19:76
Leung, Yuet-Kin; Ouyang, Bin; Niu, Liang et al. (2018) Identification of sex-specific DNA methylation changes driven by specific chemicals in cord blood in a Faroese birth cohort. Epigenetics 13:290-300
Kim, Stephani; Xu, Xijin; Zhang, Yuling et al. (2018) Metal concentrations in pregnant women and neonates from informal electronic waste recycling. J Expo Sci Environ Epidemiol :
Chen, Jing; Gálvez-Peralta, Marina; Zhang, Xiang et al. (2018) In utero gene expression in the Slc39a8(neo/neo) knockdown mouse. Sci Rep 8:10703
Abdel-Hameed, Enass A; Rouster, Susan D; Boyce, Ceejay L et al. (2018) Ultra-Deep Genomic Sequencing of HCV NS5A Resistance-Associated Substitutions in HCV/HIV Coinfected Patients. Dig Dis Sci 63:645-652

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