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Laboratoire des Interactions Plantes Micro-organismes (LIPM), Centre National de la Recherche Scientifique-Institut National de la Recherche Agronomique (CNRS-INRA) UMR 2594/441, F-31320 Castanet Tolosan, France
MtHAP2-1 is a CCAAT-binding transcription factor from the model legume Medicago truncatula. We previously showed that MtHAP2-1 expression is regulated both spatially and temporally by microRNA169. Here we present a novel regulatory mechanism controlling MtHAP2-1 expression. Alternative splicing of an intron in the MtHAP2-1 5'leader sequence (LS) becomes predominant during the development of root nodules, leading to the production of a small peptide, uORF1p. Our results indicate that binding of uORF1p to MtHAP2-1 5'LS mRNA leads to reduced accumulation of the MtHAP2-1 transcript and may contribute to spatial restriction of MtHAP2-1 expression within the nodule. We propose that miR169 and uORF1p play essential, sequential, and nonredundant roles in regulating MtHAP2-1 expression. Importantly, in contrast to previously described cis-acting uORFs, uORF1p is able to act in trans to down-regulate gene expression. Our work thus contributes to a better understanding of the action of upstream ORFs (uORFs) in the regulation of gene expression.
[Keywords: HAP2; Medicago truncatula; alternative splicing; symbiosis; transcription factor; upstream ORF]
Received October 29, 2007; revised version accepted April 8, 2008.
E-MAIL susana.rivas{at}toulouse.inra.fr; FAX 33-5-61285061.
3 E-MAIL jpcombier{at}yahoo.fr; FAX 33-5-61779412.
Supplemental material is available at http://www.genesdev.org.
Article is online at http://www.genesdev.org/cgi/doi/10.1101/gad.461808.
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