Two Zebrafish Alcohol Dehydrogenases Share Common Ancestry with Mammalian Class I, II, IV, and V Alcohol Dehydrogenase Genes but Have Distinct Functional Characteristics

Ethanol is teratogenic to many vertebrates. We are utilizing zebrafish as a model system to determine whether there is an association between ethanol metabolism and ethanol-mediated developmental toxicity. Here we report the isolation and characterization of two cDNAs encoding zebrafish alcohol dehy...

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Veröffentlicht in:The Journal of biological chemistry 2004-09, Vol.279 (37), p.38303-38312
Hauptverfasser: Reimers, Mark J., Hahn, Mark E., Tanguay, Robert L.
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creator Reimers, Mark J.
Hahn, Mark E.
Tanguay, Robert L.
description Ethanol is teratogenic to many vertebrates. We are utilizing zebrafish as a model system to determine whether there is an association between ethanol metabolism and ethanol-mediated developmental toxicity. Here we report the isolation and characterization of two cDNAs encoding zebrafish alcohol dehydrogenases (ADHs). Phylogenetic analysis of these zebrafish ADHs indicates that they share a common ancestor with mammalian class I, II, IV, and V ADHs. The genes encoding these zebrafish ADHs have been named Adh8a and Adh8b by the nomenclature committee. Both genes were genetically mapped to chromosome 13. The 1450-bp Adh8a is 82, 73, 72, and 72% similar at the amino acid level to the Baltic cod ADH8 (previously named ADH1), the human ADH1B2, the mouse ADH1, and the rat ADH1, respectively. Also, the 1484-bp Adh8b is 77, 68, 67, and 66% similar at the amino acid level to the Baltic cod ADH8, the human ADH1B2, the mouse ADH1, and the rat ADH1, respectively. ADH8A and ADH8B share 86% amino acid similarity. To characterize the functional properties of ADH8A and ADH8B, recombinant proteins were purified from SF-9 insect cells. Kinetic studies demonstrate that ADH8A metabolizes ethanol, with a Vmax of 13.4 nmol/min/mg protein, whereas ADH8B does not metabolize ethanol. The ADH8A Km for ethanol as a substrate is 0.7 mm. 4-Methyl pyrazole, a classical competitive inhibitor of class I ADH, failed to inhibit ADH8A. ADH8B has the capacity to efficiently biotransform longer chain primary alcohols (≥5 carbons) and S-hydroxymethlyglutathione, whereas ADH8A does not efficiently metabolize these substrates. Finally, mRNA expression studies indicate that both ADH8A and ADH8B mRNA are expressed during early development and in the adult brain, fin, gill, heart, kidney, muscle, and liver. Together these results indicate that class I-like ADH is conserved in zebrafish, albeit with mixed functional properties.
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subjects Alcohol Dehydrogenase - chemistry
Alcohol Dehydrogenase - genetics
Amino Acid Sequence
Animals
Binding, Competitive
Cell Line
Chromosome Mapping
Conserved Sequence
Danio rerio
DNA, Complementary - metabolism
Ethanol - pharmacology
Freshwater
Glutathione - analogs & derivatives
Glutathione - chemistry
Humans
Insecta
Kinetics
Marine
Mice
Molecular Sequence Data
Open Reading Frames
Phylogeny
Rats
Recombinant Proteins - chemistry
RNA, Messenger - metabolism
Sequence Homology, Amino Acid
Species Specificity
Time Factors
Tissue Distribution
Zebrafish
title Two Zebrafish Alcohol Dehydrogenases Share Common Ancestry with Mammalian Class I, II, IV, and V Alcohol Dehydrogenase Genes but Have Distinct Functional Characteristics
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