The long-term objective of this research is to elucidate and characterize the mechanisms responsible for tissue-specific differential gene expression using the rat class 3 aldehyde dehydrogenase as the model system.
The Specific Aims of this proposal are: (1) To complete characterization of the class 3 aldehyde dehydrogenase gene. (2) Compare organization of class 3 aldehyde dehydrogenase gene to that of mitochondrial and microsomal aldehyde dehydrogenase. (3) To determine the role of DNA methylation in class 3 aldehyde dehydrogenase gene expression. (4) To analyse the role of DNA-protein interactions in the regulation of class 3 aldehyde dehydrogenase gene expression. (5) To continue testing the hypothesis that a major physiological role for the class 3 aldehyde dehydrogenase in both neoplastic and normal cells is the oxidation of aldehydes generated from lipid peroxidation. By completing the Specific Aims outlined above, we will have completed the first detailed molecular analysis of the structural and functional organization of a gene which (a) differs in constitutive expression in normal tissues; (b) is differentially inducible in normal tissues; and (c) is differentially expressed in diseased tissues. We will also have clearly defined the mechanisms involved in these changes in expression. Lastly, we will have demonstrated how differential gene expression is related to the physiological role of the gene product.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA021103-10A3
Application #
3165445
Study Section
Medical Biochemistry Study Section (MEDB)
Project Start
1979-07-01
Project End
1994-06-30
Budget Start
1991-07-01
Budget End
1992-06-30
Support Year
10
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of South Dakota
Department
Type
Schools of Medicine
DUNS #
929930808
City
Vermillion
State
SD
Country
United States
Zip Code
57069
Reisdorph, Richard; Lindahl, Ronald (2007) Constitutive and 3-methylcholanthrene-induced rat ALDH3A1 expression is mediated by multiple xenobiotic response elements. Drug Metab Dispos 35:386-93
Reisdorph, R; Lindahl, R (2001) Aldehyde dehydrogenase 3 gene regulation: studies on constitutive and hypoxia-modulated expression. Chem Biol Interact 130-132:227-33
Canuto, R A; Ferro, M; Salvo, R A et al. (2001) Increase in class 2 aldehyde dehydrogenase expression by arachidonic acid in rat hepatoma cells. Biochem J 357:811-8
Boesch, J S; Miskimins, R; Miskimins, W K et al. (1999) The same xenobiotic response element is required for constitutive and inducible expression of the mammalian aldehyde dehydrogenase-3 gene. Arch Biochem Biophys 361:223-30
Burton, M; Reisdorph, R; Prough, R et al. (1999) Modulation of class 3 aldehyde dehydrogenase gene expression. An eye opening experience. Adv Exp Med Biol 463:165-70
Falkner, K C; Xiao, G H; Pinaire, J A et al. (1999) The negative regulation of the rat aldehyde dehydrogenase 3 gene by glucocorticoids: involvement of a single imperfect palindromic glucocorticoid responsive element. Mol Pharmacol 55:649-57
Canuto, R A; Muzio, G; Ferro, M et al. (1999) Inhibition of class-3 aldehyde dehydrogenase and cell growth by restored lipid peroxidation in hepatoma cell lines. Free Radic Biol Med 26:333-40
Lindahl, R; Xiao, G H; Falkner, K C et al. (1999) Negative regulation of rat hepatic aldehyde dehydrogenase 3 by glucocorticoids. Adv Exp Med Biol 463:159-64
Reisdorph, R; Lindahl, R (1998) Hypoxia exerts cell-type-specific effects on expression of the class 3 aldehyde dehydrogenase gene. Biochem Biophys Res Commun 249:709-12
Prough, R A; Falkner, K C; Xiao, G H et al. (1997) Regulation of rat ALDH-3 by hepatic protein kinases and glucocorticoids. Adv Exp Med Biol 414:29-36

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