This is the proposal to identify the mechanisms involved in the regulation of human alcohol dehydrogenase (ADH) gene expression. Specifically: (1) Characterization of genomic clones containing human Class 1 ADH genes will be performed to analyze the structure of this multigene family. (2) DNA probes specific for the Alpha, Beta and Gamma ADH genes will be used to determine the size and amount of mRNA transcribed from these genes in various human tissues. (3) The precise locations of the transcription initiation sites for the Class I ADH genes will be determined and the promoter-regulatory regions will be subject to DNA sequence analysis. (4) The promoter-regulatory regions of the Class I ADH genes will be fused to the easily assayable chloramphenicol acetyltransferase gene and introduced into various mammalian cell lines to assess the DNA sequences necessary for ADH gene expression. Since this class of genes exhibits a very interesting pattern of tissue specific and developmental regulation, an in-depth analysis of the promoters and regulatory regions of these genes may help shed some light on how genes are turned on and off at specific times in differentiated cells. This problem is at the heart of research in developmental biology; it underlies research on the molecular basis of cancer, and it must be resolved if gene therapy is ever to come into widespread use.
| Duester, G; Smith, M; Bilanchone, V et al. (1986) Molecular analysis of the human class I alcohol dehydrogenase gene family and nucleotide sequence of the gene encoding the beta subunit. J Biol Chem 261:2027-33 |
| Bilanchone, V; Duester, G; Edwards, Y et al. (1986) Multiple mRNAs for human alcohol dehydrogenase (ADH): developmental and tissue specific differences. Nucleic Acids Res 14:3911-26 |
| Duester, G; Jornvall, H; Hatfield, G W (1986) Intron-dependent evolution of the nucleotide-binding domains within alcohol dehydrogenase and related enzymes. Nucleic Acids Res 14:1931-41 |
