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Nucleic Acids Research 2006 34(3):986-995; doi:10.1093/nar/gkj492
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Published online 7 February 2006

© The Author 2006. 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


Article

Identification of post-transcriptionally regulated Xenopus tropicalis maternal mRNAs by microarray

Antoine Graindorge, Raphaël Thuret1, Nicolas Pollet1, H. Beverley Osborne and Yann Audic*

CNRS UMR 6061, IFR 140, Functional Genetics, Agricultural and Health Sciences, Faculté de Médecine, Université de Rennes 1 Rennes, France 1CNRS UMR 8080, Université Paris Sud Orsay, France

*To whom correspondence should be addressed at UMR 6061, Faculté de Médecine, Université de Rennes 1, 2 avenue du Professeur Léon Bernard, CS 34317, 35043 Rennes cedex, France. Tel: +33 2 2323 4475; Fax: +33 2 2323 4478; Email: yann.audic{at}univ-rennes1.fr

Received October 3, 2005. Revised December 16, 2005. Accepted January 20, 2006.

Cytoplasmic control of the adenylation state of mRNAs is a critical post-transcriptional process involved in the regulation of mRNAs stability and translational efficiency. The early development of Xenopus laevis has been a major model for the study of such regulations. We describe here a microarray analysis to identify mRNAs that are regulated by changes in their adenylation state during oogenesis and early development of the diploid frog Xenopus tropicalis. The microarray data were validated using qRT–PCR and direct analysis of the adenylation state of endogenous maternal mRNAs during the period studied. We identified more than 500 mRNAs regulated at the post-transcriptional level among the 3000 mRNAs potentially detected by the microarray. The mRNAs were classified into nine different adenylation behavior categories. The various adenylation profiles observed during oocyte maturation and early development and the analyses of 3'-untranslated region sequences suggest that previously uncharacterized sequence elements control the adenylation behavior of the newly identified mRNAs. These data should prove useful in identifying mRNAs with important functions during oocyte maturation and early development.


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