1. Novel nuclear methylation of sterols by the nematode caenorhabditis elegans
- Author
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Malcolm J. Thompson, Ruben Lozano, William R. Lusby, James A. Svoboda, and David J. Chitwood
- Subjects
Magnetic Resonance Spectroscopy ,Clinical Biochemistry ,Isomerase ,Reductase ,Methylation ,Biochemistry ,Gas Chromatography-Mass Spectrometry ,chemistry.chemical_compound ,Endocrinology ,Desmosterol ,polycyclic compounds ,Animals ,Molecular Biology ,Caenorhabditis elegans ,Pharmacology ,biology ,Organic Chemistry ,biology.organism_classification ,Sitosterols ,Sterol ,Caenorhabditis ,Sterols ,Cholesterol ,Nematode ,chemistry ,lipids (amino acids, peptides, and proteins) - Abstract
Caenorhabditis elegans possesses a unique sterol methylation pathway not reported to occur in any other organism and also removes the C-24 ethyl group of sitosterol (a plant sterol). This nematode produced substantial quantities of 4 alpha-methyl-5 alpha-cholest-8(14)-en-3 beta-ol and smaller amounts of lophenol from dietary cholesterol, desmosterol or sitosterol. When C. elegans was propagated in media containing sitosterol plus 25-azacoprostane hydrochloride (25-aza-5 beta-cholestane hydrochloride), an inhibitor of delta 24-sterol reductase in insects, its 4 alpha-methylsterol fraction largely consisted of equal amounts of 4 alpha-methyl-5 alpha-cholesta-7,24-dien-3 beta-ol and 4 alpha-methyl-5 alpha-cholesta-8(14),24-dien-3 beta-ol. Thus 25-azacoprostane hydrochloride inhibited both a delta 24-sterol reductase and a delta 7-sterol isomerase in C. elegans.
- Published
- 1983
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