The long term objectives of this research are to determine the structure of mammalian alcohol dehydrogenase genes, and to examine the mechanisms which regulate their expression. These studies will contribute to our understanding of the factors underlying differences between individuals in the metabolic, pharmacological, pathological, and psychological effects of alcohol consumption. The genetic models of formation of alcohol dehydrogenase isozymes as products of different loci will be tested in both mouse and human. Complementary DNAs representing copies of the alcohol dehydrogenase messenger RNAs will be cloned from libraries of mouse and human liver cDNA. Isolation and nucleotide sequencing of different cDNAs for the different isozymes would prove the genetic models for formation of the isozymes and provide the amino acid sequences of each. If, after extensive searching, only one type of cDNA were found it would suggest the isozymes are differently modified forms of a single polypeptide; in that case the genome would be analyzed to determine whether there were only a single locus for the structural gene for alcohol dehydrogenase. The regulation of alcohol dehydrogenase isozyme content in different tissues and strains of inbred mice will be studied by measuring enzymatic activity, protein content, and alcohol dehydrogenase mRNA content. These studies will utilize portions of the cloned cDNAs as probes for measuring mRNA content. They should reveal whether there is a strong correlation between enzyme activity and mRNA content, and whether there are structural differences in the mRNA of different tissues. This will provide evidence for or against the model that alcohol dehydrogenase activity is regulated at the level of transcription. Finally, human alcohol dehydrogenase cDNAs isolated in the proposed study will be used to explore the possibility of determining the genotype of humans at the polymorphic ADH2 and ADH3 loci.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
5R01AA006460-02
Application #
3109607
Study Section
(SRC)
Project Start
1984-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Type
Schools of Medicine
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Edenberg, Howard J; Foroud, Tatiana (2014) Genetics of alcoholism. Handb Clin Neurol 125:561-71
Criado, José R; Gizer, Ian R; Edenberg, Howard J et al. (2014) CHRNA5 and CHRNA3 variants and level of neuroticism in young adult Mexican American men and women. Twin Res Hum Genet 17:80-8
Edenberg, Howard J; Foroud, Tatiana (2013) Genetics and alcoholism. Nat Rev Gastroenterol Hepatol 10:487-94
Gizer, Ian R; Edenberg, Howard J; Gilder, David A et al. (2011) Association of alcohol dehydrogenase genes with alcohol-related phenotypes in a Native American community sample. Alcohol Clin Exp Res 35:2008-18
Edenberg, Howard J (2011) Common and rare variants in alcohol dependence. Biol Psychiatry 70:498-9
Tian, Huijun; Chen, Hui-Ju; Cross, Tiffeny H et al. (2005) Alternative splicing and promoter use in the human GABRA2 gene. Brain Res Mol Brain Res 137:174-83
Chen, Hui-Ju; Carr, Kristie; Jerome, Ronald E et al. (2002) A retroviral repetitive element confers tissue-specificity to the human alcohol dehydrogenase 1C (ADH1C) gene. DNA Cell Biol 21:793-801
Kwon, H S; Lee, D K; Lee, J J et al. (2001) Posttranscriptional regulation of human ADH5/FDH and Myf6 gene expression by upstream AUG codons. Arch Biochem Biophys 386:163-71
Zhi, X; Chan, E M; Edenberg, H J (2000) Tissue-specific regulatory elements in the human alcohol dehydrogenase 6 gene. DNA Cell Biol 19:487-97
McClintick, J; Edenberg, H J (2000) BlastReport: a perl script to facilitate the use of sequence databases for mapping and clustering. Biotechniques 29:1272-6

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