Reinforcement of silencing at transposons and highly repeated sequences requires the concerted action of two distinct RNA polymerases IV in Arabidopsis

  1. Dominique Pontier1,5,
  2. Galina Yahubyan1,5,6,
  3. Danielle Vega1,
  4. Agnès Bulski2,
  5. Julio Saez-Vasquez1,
  6. Mohamed-Ali Hakimi3,
  7. Silva Lerbs-Mache4,
  8. Vincent Colot2, and
  9. Thierry Lagrange1,7
  1. 1LGDP, UMR 5096, Université de Perpignan, 66860 Perpignan Cedex, France; 2Unité de Recherche en Génomique Végétale (URGV), INRA/CNRS/UEVE, 91057 Evry Cedex, France; 3Institut Jean Roget, 38000 Grenoble, France; 4PDC, UMR 5575, Université Joseph Fourier, 38000 Grenoble, France

Abstract

Recent genetic and biochemical studies have revealed the existence in plants of a fourth RNA polymerase, RNAPIV, which mediates siRNA accumulation and DNA methylation-dependent silencing of endogenous repeated sequences. Here, we show that Arabidopsis expresses, in fact, two evolutionarily related forms of RNAPIV, hereafter referred to as RNAPIVa and RNAPIVb. These two forms contain the same second-largest subunit (NRPD2), but differ at least by their largest subunit, termed NRPD1a and NRPD1b. Unlike NRPD1a, NRPD1b possesses a reiterated CTD, a feature that also characterizes the largest subunit of RNAPII. Our data indicate that RNAPIVb is the most abundant form of RNAPIV in Arabidopsis. Selective disruption of either form of RNAPIV indicates that RNAPIVa-dependent siRNA accumulation is not sufficient per se to drive robust silencing at endogenous loci and that high levels of DNA methylation and silencing depend on siRNA that are accumulated through a pathway involving the concerted action of both RNAPIV forms. Taken together, our results imply the existence of a novel two-step mechanism in siRNA synthesis at highly methylated loci, with RNAPIVb being an essential component of a self-reinforcing loop coupling de novo DNA methylation to siRNA production.

Keywords

Footnotes

  • Supplemental material is available at http://www.genesdev.org.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.348405.

  • 5 These authors contributed equally to this work.

  • 6 Present address: Department of Plant Physiology and Molecular Biology, University of Plovdiv, Plovdiv-4000, Bulgaria.

  • 7 Corresponding author.

    7 E-MAIL lagrange{at}univ-perp.fr; FAX 0033-0033468668499.

    • Accepted June 29, 2005.
    • Received April 25, 2005.
| Table of Contents

Life Science Alliance