articleScienceJul 6, 2006Closed access

Decay of Endoplasmic Reticulum-Localized mRNAs During the Unfolded Protein Response

QB3 · Howard Hughes Medical Institute

PubMed
Indexed incrossrefpubmed

Abstract

The unfolded protein response (UPR) allows the endoplasmic reticulum (ER) to recover from the accumulation of misfolded proteins, in part by increasing its folding capacity. Inositol-requiring enzyme-1 (IRE1) promotes this remodeling by detecting misfolded ER proteins and activating a transcription factor, X-box-binding protein 1, through endonucleolytic cleavage of its messenger RNA (mRNA). Here, we report that IRE1 independently mediates the rapid degradation of a specific subset of mRNAs, based both on their localization to the ER membrane and on the amino acid sequence they encode. This response is well suited to complement other UPR mechanisms because it could selectively halt production of proteins that…

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1,300
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16.88
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100%
References
29
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Authors

2

Topics & keywords

Keywords
  • Endoplasmic reticulum
  • Unfolded protein response
  • Cell biology
  • Protein folding
  • Messenger RNA
  • Chemistry
  • Biology
  • Biochemistry
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