Fig. 1.
Fig. 1. Translational regulation of ferritin synthesis, which applies to both the H and L subunit. (A) A single functional IRE is found in the 5′ UTR of the genes encoding ferritin H and L subunits, and this noncoding sequence behaves as an mRNA cis-acting element. The other component of this regulatory system is a specific trans-acting cytoplasmic binding protein, called iron regulatory protein (IRP; two IRPs, IRP-1 and IRP-2, have been identified so far). When cellular iron is scarce, IRP binds to IRE, where it inhibits ferritin translation. When cellular iron is abundant, formation of [4Fe-4S] clusters within IRP prevents binding to IRE; as a consequence, ferritin synthesis is allowed. The reader is referred to the comprehensive review by Klausner et al8 for details. (B) Sequence and proposed structure of ferritin L-subunit IRE. The reader is referred to the comprehensive review by Theil9 for details. The IRE bulge has been depicted according to Butt et al.10

Translational regulation of ferritin synthesis, which applies to both the H and L subunit. (A) A single functional IRE is found in the 5′ UTR of the genes encoding ferritin H and L subunits, and this noncoding sequence behaves as an mRNA cis-acting element. The other component of this regulatory system is a specific trans-acting cytoplasmic binding protein, called iron regulatory protein (IRP; two IRPs, IRP-1 and IRP-2, have been identified so far). When cellular iron is scarce, IRP binds to IRE, where it inhibits ferritin translation. When cellular iron is abundant, formation of [4Fe-4S] clusters within IRP prevents binding to IRE; as a consequence, ferritin synthesis is allowed. The reader is referred to the comprehensive review by Klausner et al8 for details. (B) Sequence and proposed structure of ferritin L-subunit IRE. The reader is referred to the comprehensive review by Theil9 for details. The IRE bulge has been depicted according to Butt et al.10 

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