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Nucleic Acids Research 2006 33(22):7138-7150; doi:10.1093/nar/gki1012
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Published online 3 January 2006

© The Author 2005. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oxfordjournals.org


Survey and Summary

AU-rich elements and associated factors: are there unifying principles?

Carine Barreau, Luc Paillard and H. Beverley Osborne*

UMR 6061 CNRS Génétique et Développement, IFR 140 Génétique Fonctionnelle Agronomie et Santé, Université de Rennes 1, Faculté de Médecine CS 34317, 35043 Rennes cedex, France

*To whom correspondence should be addressed. Tel: +33 223 23 4523; Fax: +33 223 23 4478; Email: Beverley.osborne{at}univ-rennes1.fr

Received September 17, 2005. Revised November 5, 2005. Accepted November 25, 2005.

The control of mRNA stability is an important process that allows cells to not only limit, but also rapidly adjust, the expression of regulatory factors whose over expression may be detrimental to the host organism. Sequence elements rich in A and U nucleotides or AU-rich elements (AREs) have been known for many years to target mRNAs for rapid degradation. In this survey, after briefly summarizing the data on the sequence characteristics of AREs, we present an analysis of the known ARE-binding proteins (ARE-BP) with respect to their mRNA targets and the consequences of their binding to the mRNA. In this analysis, both the changes in mRNA stability and the lesser studied effects on translation are considered. This analysis highlights the multitude of mRNAs bound by one ARE-BP and conversely the large number of ARE-BP that associate with any particular ARE-containing mRNA. This situation is discussed with respect to functional redundancies or antagonisms. The potential relationship between mRNA stability and translation is also discussed. Finally, we present several hypotheses that could unify the published data and suggest avenues for future research.


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