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Biological Chemistry

Editor-in-Chief: Brüne, Bernhard

Editorial Board: Buchner, Johannes / Lei, Ming / Ludwig, Stephan / Thomas, Douglas D. / Turk, Boris / Wittinghofer, Alfred


IMPACT FACTOR 2018: 3.014
5-year IMPACT FACTOR: 3.162

CiteScore 2018: 3.09

SCImago Journal Rank (SJR) 2018: 1.482
Source Normalized Impact per Paper (SNIP) 2018: 0.820

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1437-4315
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Volume 389, Issue 3

Issues

Posttranscriptional gene regulation by RNA-binding proteins during oxidative stress: implications for cellular senescence

Kotb Abdelmohsen
  • 1Laboratory of Cellular and Molecular Biology, National Institute on Aging – Intramural Research Program, National Institutes of Health, Baltimore, MD 21228, USA
  • Other articles by this author:
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/ Yuki Kuwano
  • 2Laboratory of Cellular and Molecular Biology, National Institute on Aging – Intramural Research Program, National Institutes of Health, Baltimore, MD 21228, USA
  • Other articles by this author:
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/ Hyeon Ho Kim
  • 3Laboratory of Cellular and Molecular Biology, National Institute on Aging – Intramural Research Program, National Institutes of Health, Baltimore, MD 21228, USA
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/ Myriam Gorospe
  • 4Laboratory of Cellular and Molecular Biology, National Institute on Aging – Intramural Research Program, National Institutes of Health, Baltimore, MD 21228, USA
  • Other articles by this author:
  • De Gruyter OnlineGoogle Scholar
Published Online: 2008-03-03 | DOI: https://doi.org/10.1515/BC.2008.022

Abstract

To respond adequately to oxidative stress, mammalian cells elicit rapid and tightly controlled changes in gene expression patterns. Besides alterations in the subsets of transcribed genes, two posttranscriptional processes prominently influence the oxidant-triggered gene expression programs: mRNA turnover and translation. Here, we review recent progress in our knowledge of the turnover and translation regulatory (TTR) mRNA-binding proteins (RBPs) that influence gene expression in response to oxidative damage. Specifically, we identify oxidant damage-regulated mRNAs that are targets of TTR-RBPs, we review the oxidant-triggered signaling pathways that govern TTR-RBP function, and we examine emerging evidence that TTR-RBP activity is altered with senescence and aging. Given the potent influence of TTR-RBPs upon oxidant-regulated gene expression profiles, we propose that the senescence-associated changes in TTR-RBPs directly contribute to the impaired responses to oxidant damage that characterize cellular senescence and advancing age.

Keywords: mRNA stability; posttranscriptional gene regulation; reactive oxygen species (ROS) signaling pathway; RNA-binding proteins; translational control

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Corresponding author


Published Online: 2008-03-03

Published in Print: 2008-03-01


Citation Information: Biological Chemistry, Volume 389, Issue 3, Pages 243–255, ISSN (Online) 14374315, ISSN (Print) 14316730, DOI: https://doi.org/10.1515/BC.2008.022.

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