Literature DB >> 20026480

The increase in the number of subunits in eukaryotic RNA polymerase III relative to RNA polymerase II is due to the permanent recruitment of general transcription factors.

Robert Carter1, Guy Drouin.   

Abstract

The number of subunits of RNA polymerases (RNAPs) increases during evolution from 5 in eubacteria to 12 in archaea. In eukaryotes, which have at least three RNAPs, the number of subunits has expanded from 12 in RNA polymerase II (RNAPII) to 14 in RNA polymerase I (RNAPI) and to 17 in RNA polymerase III (RNAPIII). It was recently demonstrated that the two additional subunits found in RNAPI relative to RNAPII are homologous to TFIIF, a dimeric general transcription factor of RNAPII. Here, we extend this finding by demonstrating that four of the five RNAPIII-specific subunits are also homologous to transcription factors of RNAPII. We use the available evidence to propose an evolutionary history of the eukaryotic RNAPs and argue that the increases in the number of subunits that occurred in RNAPs I and III are due to the permanent recruitment of preexisting transcription factors.

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Year:  2009        PMID: 20026480     DOI: 10.1093/molbev/msp316

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  43 in total

1.  Conformational flexibility of RNA polymerase III during transcriptional elongation.

Authors:  Carlos Fernández-Tornero; Bettina Böttcher; Umar Jan Rashid; Ulrich Steuerwald; Beate Flörchinger; Damien P Devos; Doris Lindner; Christoph W Müller
Journal:  EMBO J       Date:  2010-10-22       Impact factor: 11.598

2.  A high density of cis-information terminates RNA Polymerase III on a 2-rail track.

Authors:  Aneeshkumar G Arimbasseri; Richard J Maraia
Journal:  RNA Biol       Date:  2015-12-04       Impact factor: 4.652

3.  Crystal structure of the 14-subunit RNA polymerase I.

Authors:  Carlos Fernández-Tornero; María Moreno-Morcillo; Umar J Rashid; Nicholas M I Taylor; Federico M Ruiz; Tim Gruene; Pierre Legrand; Ulrich Steuerwald; Christoph W Müller
Journal:  Nature       Date:  2013-10-23       Impact factor: 49.962

4.  The TFIIF-like Rpc37/53 dimer lies at the center of a protein network to connect TFIIIC, Bdp1, and the RNA polymerase III active center.

Authors:  Chih-Chien Wu; Yu-Chun Lin; Hung-Ta Chen
Journal:  Mol Cell Biol       Date:  2011-05-02       Impact factor: 4.272

5.  Structure-function analysis of hRPC62 provides insights into RNA polymerase III transcription initiation.

Authors:  Stéphane Lefèvre; Hélène Dumay-Odelot; Leyla El-Ayoubi; Aidan Budd; Pierre Legrand; Noël Pinaud; Martin Teichmann; Sébastien Fribourg
Journal:  Nat Struct Mol Biol       Date:  2011-02-27       Impact factor: 15.369

6.  General transcription factors and subunits of RNA polymerase III: Paralogs for promoter- and cell type-specific transcription in multicellular eukaryotes.

Authors:  Martin Teichmann; Giorgio Dieci; Chiara Pascali; Galina Boldina
Journal:  Transcription       Date:  2010-07-30

7.  Analyzing RNA polymerase III by electron cryomicroscopy.

Authors:  Carlos Fernández-Tornero; Bettina Böttcher; Umar Jan Rashid; Christoph W Müller
Journal:  RNA Biol       Date:  2011-09-01       Impact factor: 4.652

Review 8.  Cell growth- and differentiation-dependent regulation of RNA polymerase III transcription.

Authors:  Hélène Dumay-Odelot; Stéphanie Durrieu-Gaillard; Daniel Da Silva; Robert G Roeder; Martin Teichmann
Journal:  Cell Cycle       Date:  2010-09-01       Impact factor: 4.534

Review 9.  Comparative overview of RNA polymerase II and III transcription cycles, with focus on RNA polymerase III termination and reinitiation.

Authors:  Aneeshkumar G Arimbasseri; Keshab Rijal; Richard J Maraia
Journal:  Transcription       Date:  2014

Review 10.  Transcription termination by the eukaryotic RNA polymerase III.

Authors:  Aneeshkumar G Arimbasseri; Keshab Rijal; Richard J Maraia
Journal:  Biochim Biophys Acta       Date:  2012-10-23
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