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Nucleic Acids Research Advance Access originally published online on December 19, 2006
Nucleic Acids Research 2007 35(2):634-647; doi:10.1093/nar/gkl686
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Nucleic Acids Research, 2007, Vol. 35, No. 2 634-647
© 2006 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Nucleic Acid Enzymes

Functional organization of the Rpb5 subunit shared by the three yeast RNA polymerases

Cécile Zaros1, Jean-François Briand1, Yves Boulard1, Sylvie Labarre-Mariotte1, M. Carmen Garcia-Lopez2, Pierre Thuriaux1,* and Francisco Navarro2,*

1 Service de Biochimie & Génétique Moléculaire. Bâtiment 144 CEA-Saclay, F-91191, Gif-sur-Yvette, CEDEX, France 2 Department Biología Experimental—Area de Genética (ED.B3) Universidad de Jaén Paraje las Lagunillas E-23071 Jaén, SPAIN

*To whom correspondence should be addressed. Tel: +33 1 69 08 35 86; Fax: +33 1 69 08 47 12; Email: pierre.thuriaux{at}cea.fr

Received May 3, 2006. Revised July 30, 2006. Accepted September 7, 2006.

Rpb5, a subunit shared by the three yeast RNA polymerases, combines a eukaryotic N-terminal module with a globular C-end conserved in all non-bacterial enzymes. Conditional and lethal mutants of the moderately conserved eukaryotic module showed that its large N-terminal helix and a short motif at the end of the module are critical in vivo. Lethal or conditional mutants of the C-terminal globe altered the binding of Rpb5 to Rpb1-ß25/26 (prolonging the Bridge helix) and Rpb1-{alpha}44/47 (ahead of the Switch 1 loop and binding Rpb5 in a two-hybrid assay). The large intervening segment of Rpb1 is held across the DNA Cleft by Rpb9, consistent with the synergy observed for rpb5 mutants and rpb9{Delta} or its RNA polymerase I rpa12{Delta} counterpart. Rpb1-ß25/26, Rpb1-{alpha}44/45 and the Switch 1 loop were only found in Rpb5-containing polymerases, but the Bridge and Rpb1-{alpha}46/47 helix bundle were universally conserved. We conclude that the main function of the dual Rpb5–Rpb1 binding and the Rpb9–Rpb1 interaction is to hold the Bridge helix, the Rpb1-{alpha}44/47 helix bundle and the Switch 1 loop into a closely packed DNA-binding fold around the transcription bubble, in an organization shared by the two other nuclear RNA polymerases and by the archaeal and viral enzymes.


*Correspondence may also be addressed to Francisco Navarro. Tel: 34 9 53 21 27 71; Fax: 34 9 53 21 18 75; Email: fngomez{at}ujaen.es


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