Abstract
IRON administration increases the net synthesis of apoferritin in rat liver in vivo1. Correspondingly, liver slices prepared from rats dosed with iron incorporate 14C-leucine into apoferritin in vitro more readily than do slices from untreated controls2. The mechanism by which the iron acts is unknown, although it has been postulated that intracellular iron in erythroblasts may influence genetic loci3. In the following experiments actinomycin D, an inhibitor of DNA-dependent RNA synthesis4, was administered to rats prior to a dose of iron, and liver slices were later tested in vitro for incorporation of 14C-leucine into apoferritin. Actinomycin D inhibited the stimulatory effect of iron, indicating that derepression of genes and the synthesis of messenger RNA are involved in the regulatory response to the metal.
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YOSHINO, Y., MANIS, J. & SCHACHTER, D. Actinomycin D and the Regulation of Apoferritin Synthesis in Rat Liver. Nature 210, 538–539 (1966). https://doi.org/10.1038/210538b0
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DOI: https://doi.org/10.1038/210538b0
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