The University of Arizona (U of A) proposes the establishment of a Human Genes and the Environment Research (HuGER) Training Program. Development of the HuGER training program has been guided by several important realities. Most relevant to the HuGER TG is recognition of the fact that in the coming decades, a more precise determination of the influence of environmental exposures within a given genetic background on disease processes will be required to significantly improve pur ability to predict, detect, treat and monitor disease progression and disease response. In addition it is increasingly clear that epigenetic status will emerge as a critical process that is modulated by environmental exposures, leading to the adverse or beneficial manifestation of that exposure. The HuGER will build upon three inter-disciplinary pre-, and post-doctoral training programs integral to the creation of a successful multi-disciplinary training program that rains scientists in environmental genomics/genetics. An (i) NIEHS supported inter-disciplinary training Drogram in Toxicogenomics and Toxicology, an (ii) NSF Interdisciplinary Graduate Education and Research Training (IGERT) Program in Evolutionary, Functional, and Computational Genomics, and (iii) a Graduate nterdisciplinary Program (GIDP) in Statistics provide the foundation for the evolution of this multi-disciplinary nitiative. The HuGER curriculum has been created specifically to address the unique requirements of a multi-disciplinary training program, the cornerstone of which includes two new courses, redesigning additional courses, "industrial" research rotations, and an emphasis on the development of competent and effective communicators. This is especially important for the new generation of scientists who will need to communicate effectively across multi-disciplinary boundaries. The training environment at the U of A also Drovides trainees with access to appropriate contemporary computing and state-of-the-art technologies. The Training Program Faculty consist of a core of 17 scientists, from 10 departments, with active research programs in the areas of (i) the environmental and public health sciences and engineering, (ii) population and functional genomics/genetics, and (iii) computational biology and statistics/bioinformatics. Six principal units are participating in the HuGER Training Program: [1] the College of Agriculture and Life Sciences;[2 the College of Engineering;[3] the College of Medicine [4] the College of Pharmacy;[5] the College of Public Health;and [6] the College of Sciences. Five of these Colleges participate in the BIOS Institute which brings together scientists from disparate disciplines to solve complex biological problems. The Associate Director a this HuGER application, Dr. Vicki Chandler, is the Director of BIOS. To ensure the program is known for it multidisciplinary emphasis, it will be administratively housed within BIOS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Institutional National Research Service Award (T32)
Project #
5T32ES016652-05
Application #
8307533
Study Section
Special Emphasis Panel (ZES1-LWJ-G (TG))
Program Officer
Shreffler, Carol K
Project Start
2008-07-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2014-06-30
Support Year
5
Fiscal Year
2012
Total Cost
$178,033
Indirect Cost
$20,574
Name
University of Arizona
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Monks, Terrence J; Lau, Serrine S (2013) Reactive intermediates: molecular and MS-based approaches to assess the functional significance of chemical-protein adducts. Toxicol Pathol 41:315-21
Kimzey, Michael J; Yassine, Hussein N; Riepel, Brent M et al. (2011) New site(s) of methylglyoxal-modified human serum albumin, identified by multiple reaction monitoring, alter warfarin binding and prostaglandin metabolism. Chem Biol Interact 192:122-8
Kimzey, Michael J; Zarate, Xristo; Galbraith, David W et al. (2011) Optimizing microarray-based in situ transcription-translation of proteins for matrix-assisted laser desorption ionization mass spectrometry. Anal Biochem 414:282-6
Cohen, Jennifer D; Tham, Kimberly Y; Mastrandrea, Nicholas J et al. (2011) cAMP-dependent cytosolic mislocalization of p27(kip)-cyclin D1 during quinol-thioether-induced tuberous sclerosis renal cell carcinoma. Toxicol Sci 122:361-71
Bolt, Alicia M; Byrd, Randi M; Klimecki, Walter T (2010) Autophagy is the predominant process induced by arsenite in human lymphoblastoid cell lines. Toxicol Appl Pharmacol 244:366-73
Bolt, Alicia M; Douglas, Randi M; Klimecki, Walter T (2010) Arsenite exposure in human lymphoblastoid cell lines induces autophagy and coordinated induction of lysosomal genes. Toxicol Lett 199:153-9