PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 21, 1989Science382 citations

Oxidation-Reduction and the Molecular Mechanism of a Regulatory RNA-Protein Interaction

View Full Paper
Matthias W. Hentze
Matthias W. HentzeTufts University
TRTracey A. RouaultCentre d'Études Scientifiques et Techniques d'AquitaineJHJoe B. HarfordAllogene Therapeutics (United States)

Key Points

Key points are not available for this paper at this time.

Abstract

Iron-responsive elements (IREs) are RNA motifs that have been identified within the 5' untranslated region of ferritin messenger RNA and the 3' untranslated region of transferrin receptor mRNA. A single IRE mediates iron-dependent control of ferritin translation, whereas multiple IREs are found in the region of the transferrin receptor mRNA responsible for iron-dependent control of mRNA stability. A cytosolic protein binds in vitro to the IREs of both mRNAs. The IRE-binding protein (IRE-BP) is shown to require free sulfhydryl groups for its specific interaction with the IRE. Treatment of lysates with reducing agents increases the binding activity, whereas agents that block sulfhydryls inhibit binding. Iron starvation, leading to decreased ferritin translation, results in increased binding activity, which is explained by an increase in the fraction of the IRE-BP that is in a fully reduced state.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Hentze et al. (1989) studied this question.

synapsesocial.com/papers/6a1a94724dcca27063858f96https://doi.org/10.1126/science.2711187
Ask AI
Helpful
Bookmark
Share
View Full Paper