Literature DB >> 2774571

Retinoic acid synthesis by cytosol from the alcohol dehydrogenase negative deermouse.

K C Posch1, W J Enright, J L Napoli.   

Abstract

Cytosolic alcohol dehydrogenase in the deermouse is coded by a single genetic locus and a strain of the deermouse which is alcohol dehydrogenase negative exists. These two strains of the deermouse were used to extend insight into the role of cytosolic alcohol dehydrogenases in the conversion of retinol into retinoic acid. Retinoic acid synthesis from physiological concentrations of retinol (7.5 microM) with cytosol from the alcohol dehydrogenase negative deermouse was 13% (liver), 14% (kidney), 60% (testes), 78% (lung), and 100% (small intestinal mucosa) of that observed with cytosol from the positive deermouse. The rates in the negative strain ranged from 0.3 to 0.7 nmol/h/mg protein: sufficient to fulfill cellular needs for retinoic acid. Ten millimolar 4-methylpyrazole inhibited retinoic acid synthesis 92, 94, 26, and 30% in kidney, liver, lung, and testes of the positive deermouse, respectively, but only 50, 30, 0, and 0% in the same tissues from the negative deermouse. Ethanol (300 mM) did not inhibit retinoic acid synthesis in kidney cytosol from the negative strain. Therefore multiple cytosolic dehydrogenases, including alcohol dehydrogenases, contribute to retinol metabolism in vitro. The only enzyme(s) likely to be physiologically significant to retinoic acid synthesis in vivo, however, is the class of dehydrogenase, distinct from ethanol dehydrogenase, that is common to both the positive and the negative deermouse. This conclusion is supported by the data described above, the kinetics of retinoic acid synthesis and retinal reduction in kidney cytosol from the negative deermouse, and the very existence of the alcohol dehydrogenase negative deermouse. This work also shows that microsomes inhibit the cytosolic conversion of retinol into retinoic acid and that the synthesis of retinal, a retinoid that has no known function outside of the eye, does not reflect the ability or capacity of a sample to synthesize retinoic acid.

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Year:  1989        PMID: 2774571     DOI: 10.1016/0003-9861(89)90428-1

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  6 in total

1.  A dominant negative mutation of the alpha retinoic acid receptor gene in a retinoic acid-nonresponsive embryonal carcinoma cell.

Authors:  M A Pratt; J Kralova; M W McBurney
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

Review 2.  Functions of Intracellular Retinoid Binding-Proteins.

Authors:  Joseph L Napoli
Journal:  Subcell Biochem       Date:  2016

3.  Retinol and retinal metabolism. Relationship to the state of differentiation of cultured human keratinocytes.

Authors:  G Siegenthaler; J H Saurat; M Ponec
Journal:  Biochem J       Date:  1990-06-01       Impact factor: 3.857

4.  4-Methylpyrazole partially ameliorated the teratogenicity of retinol and reduced the metabolic formation of all-trans-retinoic acid in the mouse.

Authors:  M D Collins; C Eckhoff; I Chahoud; G Bochert; H Nau
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

5.  Retinoic acid response element in the human alcohol dehydrogenase gene ADH3: implications for regulation of retinoic acid synthesis.

Authors:  G Duester; M L Shean; M S McBride; M J Stewart
Journal:  Mol Cell Biol       Date:  1991-03       Impact factor: 4.272

6.  Retinoic acid synthesis and functions in early embryonic development.

Authors:  Richard Kin Ting Kam; Yi Deng; Yonglong Chen; Hui Zhao
Journal:  Cell Biosci       Date:  2012-03-22       Impact factor: 7.133

  6 in total

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