The action of ARGONAUTE1 in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development

  1. Hervé Vaucheret1,2,6,
  2. Franck Vazquez1,3,
  3. Patrice Crété3,5, and
  4. David P. Bartel2,4,7
  1. 1Laboratoire de Biologie Cellulaire, Institut Jean-Pierre Bourgin, INRA, 78026 Versailles Cedex, France; 2Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA; 3Laboratoire de physiologie de la différenciation végétale, UPRES-EA3569, IFR118, EPT1016, Université des Sciences et Technologies de Lille, 59650 Villeneuve d'Ascq Cedex, France; 4Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA

Abstract

MicroRNAs (miRNAs) are endogenous 21–24-nt RNAs that can down-regulate gene expression by pairing to the messages of protein-coding genes to specify mRNA cleavage or repression of productive translation. They act within the RNA-induced silencing complex (RISC), which in animals contains a member of the Argonaute family of proteins. In the present study, we show that Arabidopsis ago1 mutants have increased accumulation of mRNAs known to be targeted for cleavage by miRNAs. In hypomorphic ago1 alleles, this compromised miRNA function occurs without a substantial change in miRNA accumulation, whereas in null alleles it is accompanied by a drop in some of the miRNAs. Therefore, AGO1 acts within the Arabidopsis miRNA pathway, probably within the miRNA-programmed RISC, such that the absence of AGO1 destabilizes some of the miRNAs. We also show that targeting of AGO1 mRNA by miR168 is needed for proper plant development, illustrating the importance of feedback control by this miRNA. Transgenic plants expressing a mutant AGO1 mRNA with decreased complementarity to miR168 overaccumulate AGO1 mRNA and exhibit developmental defects partially overlapping with those of dcl1, hen1, and hyl1 mutants showing a decrease in miRNA accumulation. miRNA targets overaccumulate in miR168-resistant plants, suggesting that a large excess of AGO1 protein interferes with the function of RISC or sequesters miRNAs or other RISC components. Developmental defects induced by a miR168-resistant AGO1 mRNA can be rescued by a compensatory miRNA that is complementary to the mutant AGO1 mRNA, proving the regulatory relationship between miR168 and its target and opening the way for engineering artificial miRNAs in plants.

Keywords

Footnotes

  • Article published online ahead of print. Article and publication date are at http://www.genesdev.org/cgi/doi/10.1101/gad.1201404.

  • 5 Present addresses:

    5 Laboratoire de Génétique et Biophysiques des Plantes, UMR 163 CEA-CNRS-Universitá de la Méditerranée, 13288 Marseille cedex 9, France.

  • Corresponding authors.

  • 6 E-MAIL herve.vaucheret{at}versailles.inra.fr; FAX 33-1-3083-3099.

  • 7 E-MAIL dbartel{at}wi.mit.edu; FAX (617) 258-6768.

    • Accepted April 5, 2004.
    • Received March 8, 2004.
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