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RNA polymerase I-specific subunits promote polymerase clustering to enhance the rRNA gene transcription cycle

Authors :
Christophe Normand
Isabelle Léger-Silvestre
Benjamin Albert
Jorge Perez-Fernandez
Kostya I. Panov
Joost C. B. M. Zomerdijk
Patrick Schultz
Martin K. Ostermaier
Olivier Gadal
Laboratoire de biologie moléculaire eucaryote (LBME)
Centre National de la Recherche Scientifique (CNRS)-Centre de Biologie Intégrative (CBI)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)
Division of Gene Regulation and Expression, School of Life Sciences
University of Dundee
Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)
Source :
Journal of Cell Biology, Journal of Cell Biology, Rockefeller University Press, 2011, 192 (2), pp.277-93. ⟨10.1083/jcb.201006040⟩, The Journal of Cell Biology
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

The Pol I subunits Rpa34 and Rpa49, required for elongation and 35S rRNA production, promote clustering of neighboring Pol I complexes to enhance the rRNA gene transcription cycle.<br />RNA polymerase I (Pol I) produces large ribosomal RNAs (rRNAs). In this study, we show that the Rpa49 and Rpa34 Pol I subunits, which do not have counterparts in Pol II and Pol III complexes, are functionally conserved using heterospecific complementation of the human and Schizosaccharomyces pombe orthologues in Saccharomyces cerevisiae. Deletion of RPA49 leads to the disappearance of nucleolar structure, but nucleolar assembly can be restored by decreasing ribosomal gene copy number from 190 to 25. Statistical analysis of Miller spreads in the absence of Rpa49 demonstrates a fourfold decrease in Pol I loading rate per gene and decreased contact between adjacent Pol I complexes. Therefore, the Rpa34 and Rpa49 Pol I–specific subunits are essential for nucleolar assembly and for the high polymerase loading rate associated with frequent contact between adjacent enzymes. Together our data suggest that localized rRNA production results in spatially constrained rRNA production, which is instrumental for nucleolar assembly.

Details

Language :
English
ISSN :
00219525 and 15408140
Database :
OpenAIRE
Journal :
Journal of Cell Biology, Journal of Cell Biology, Rockefeller University Press, 2011, 192 (2), pp.277-93. ⟨10.1083/jcb.201006040⟩, The Journal of Cell Biology
Accession number :
edsair.doi.dedup.....b35f9d1478789cb0efbfdef9832f965c
Full Text :
https://doi.org/10.1083/jcb.201006040⟩