ZBP1 regulates mRNA stability during cellular stress

J Cell Biol. 2006 Nov 20;175(4):527-34. doi: 10.1083/jcb.200608071. Epub 2006 Nov 13.

Abstract

An essential constituent of the integrated stress response (ISR) is a reversible translational suppression. This mRNA silencing occurs in distinct cytoplasmic foci called stress granules (SGs), which transiently associate with processing bodies (PBs), typically serving as mRNA decay centers. How mRNAs are protected from degradation in these structures remains elusive. We identify that Zipcode-binding protein 1 (ZBP1) regulates the cytoplasmic fate of specific mRNAs in nonstressed cells and is a key regulator of mRNA turnover during the ISR. ZBP1 association with target mRNAs in SGs was not essential for mRNA targeting to SGs. However, ZBP1 knockdown induced a selective destabilization of target mRNAs during the ISR, whereas forced expression increased mRNA stability. Our results indicate that although targeting of mRNAs to SGs is nonspecific, the stabilization of mRNAs during cellular stress requires specific protein-mRNA interactions. These retain mRNAs in SGs and prevent premature decay in PBs. Hence, mRNA-binding proteins are essential for translational adaptation during cellular stress by modulating mRNA turnover.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Proteins / metabolism*
  • Chickens
  • Cytoplasmic Granules / metabolism
  • Humans
  • Protein Binding
  • Protein Transport
  • RNA Stability*
  • RNA-Binding Proteins / metabolism*
  • Sequence Deletion / genetics

Substances

  • Avian Proteins
  • RNA-Binding Proteins
  • ZBP1 protein, Gallus gallus