? ? The metal response element-binding transcription factor-1 (MTF-1) is a ubiquitously expressed transcription factor that plays a primary role in the regulation of a variety of genes involved in metal homeostasis, embryonic development, tumor progression, and oxidative stress or hypoxia signaling. The overall objective of this research is to characterize the overlapping role of MTF-1 with Nuclear erythroid 2 p45-related factor 2 (NRF2), the primary transcription factor for regulating the oxidative stress response, in development and transcriptional co-regulation of stress responsive genes. The investigator's goal for this award is to obtain advanced training in molecular and transgenic techniques utilizing the zebrafish as a model organism for developmental toxicology. These techniques will include morpholino knockdown of gene expression, development of transgenic zebrafish lines, gene expression profiling with oligonucleotide microarrays, and advanced bioinformatic techniques for microarray analysis and computational promoter analysis. The investigator will expand background in environmental/ecological toxicogenomics by applying these techniques to the study of transcription factors that play fundamental roles in the cellular response to metal or oxidative stress. This experience will assist the investigator in the future goal of establishing an independent research laboratory, where molecular and genomic techniques will be utilized to continue research in developmental and molecular toxicology and gene regulatory networks. Training during the mentor phase of this award will be directed by Dr. Mark Hahn (Woods Hole Oceanographic Institution, WHOI), an internationally recognized molecular toxicologist with two decades of research experience in the characterization of transcriptipon factors in a variety of model organisms. WHOI is a world-renowned center of scientific research. Under the guidance of Dr. Hahn, and with consultation from Dr. Elwood Linney (Duke University), the investigator will fully characterize the transactivation domain of MTF-1 and generate a germline transgenic zebrafish that inhibits endogenous MTF-1 signaling through the expression of a dominant-negative construct. In addition to learning advanced zebrafish techniques, time in the mentored phase will involve additional training through formal coursework and seminars, as well as further guidance in grantsmanship that will assist the investigator in transition to an independent researcher. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Career Transition Award (K99)
Project #
1K99ES017044-01
Application #
7571754
Study Section
Special Emphasis Panel (ZES1-JAB-C (KR))
Program Officer
Shreffler, Carol K
Project Start
2008-09-29
Project End
2009-08-31
Budget Start
2008-09-29
Budget End
2009-08-31
Support Year
1
Fiscal Year
2008
Total Cost
$79,388
Indirect Cost
Name
Woods Hole Oceanographic Institution
Department
Type
DUNS #
001766682
City
Woods Hole
State
MA
Country
United States
Zip Code
02543
O'Shields, Britton; McArthur, Andrew G; Holowiecki, Andrew et al. (2014) Inhibition of endogenous MTF-1 signaling in zebrafish embryos identifies novel roles for MTF-1 in development. Biochim Biophys Acta 1843:1818-33
Zanette, Juliano; Jenny, Matthew J; Goldstone, Jared V et al. (2009) New cytochrome P450 1B1, 1C2 and 1D1 genes in the killifish Fundulus heteroclitus: Basal expression and response of five killifish CYP1s to the AHR agonist PCB126. Aquat Toxicol 93:234-43
Jenny, Matthew J; Karchner, Sibel I; Franks, Diana G et al. (2009) Distinct roles of two zebrafish AHR repressors (AHRRa and AHRRb) in embryonic development and regulating the response to 2,3,7,8-tetrachlorodibenzo-p-dioxin. Toxicol Sci 110:426-41