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EMBO J. 1993 Sep;12(9):3651-7.

Translational regulation via iron-responsive elements by the nitric oxide/NO-synthase pathway.

Author information

1
Gene Expression Programme, European Molecular Biology Laboratory, Heidelberg, Germany.

Abstract

Nitric oxide (NO) produced from L-arginine by NO synthases (NOS) is a transmitter known to be involved in diverse biological processes, including immunomodulation, neurotransmission and blood vessel dilatation. We describe a novel role of NO as a signaling molecule in post-transcriptional gene regulation. We demonstrate that induction of NOS in macrophage and non-macrophage cell lines activates RNA binding by iron regulatory factor (IRFs), the central trans regulator of mRNAs involved in cellular iron metabolism. NO-induced binding of IRF to iron-responsive elements (IRE) specifically represses the translation of transfected IRE-containing indicator mRNAs as well as the biosynthesis of the cellular iron storage protein ferritin. These findings define a new biological function of NO and identify a regulatory connection between the NO/NOS pathway and cellular iron metabolism.

PMID:
7504627
PMCID:
PMC413641
[Indexed for MEDLINE]
Free PMC Article

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