Literature DB >> 8246845

Genetics of eukaryotic RNA polymerases I, II, and III.

J Archambault1, J D Friesen.   

Abstract

The transcription of nucleus-encoded genes in eukaryotes is performed by three distinct RNA polymerases termed I, II, and III, each of which is a complex enzyme composed of more than 10 subunits. The isolation of genes encoding subunits of eukaryotic RNA polymerases from a wide spectrum of organisms has confirmed previous biochemical and immunological data indicating that all three enzymes are closely related in structures that have been conserved in evolution. Each RNA polymerase is an enzyme complex composed of two large subunits that are homologous to the two largest subunits of prokaryotic RNA polymerases and are associated with smaller polypeptides, some of which are common to two or to all three eukaryotic enzymes. This remarkable conservation of structure most probably underlies a conservation of function and emphasizes the likelihood that information gained from the study of RNA polymerases from one organism will be applicable to others. The recent isolation of many mutations affecting the structure and/or function of eukaryotic and prokaryotic RNA polymerases now makes it feasible to begin integrating genetic and biochemical information from various species in order to develop a picture of these enzymes. The picture of eukaryotic RNA polymerases depicted in this article emphasizes the role(s) of different polypeptide regions in interaction with other subunits, cofactors, substrates, inhibitors, or accessory transcription factors, as well as the requirement for these interactions in transcription initiation, elongation, pausing, termination, and/or enzyme assembly. Most mutations described here have been isolated in eukaryotic organisms that have well-developed experimental genetic systems as well as amenable biochemistry, such as Saccharomyces cerevisiae, Drosophila melanogaster, and Caenorhabditis elegans. When relevant, mutations affecting regions of Escherichia coli RNA polymerase that are conserved among eukaryotes and prokaryotes are also presented. In addition to providing information about the structure and function of eukaryotic RNA polymerases, the study of mutations and of the pleiotropic phenotypes they imposed has underscored the central role played by these enzymes in many fundamental processes such as development and cellular differentiation.

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Year:  1993        PMID: 8246845      PMCID: PMC372932          DOI: 10.1128/mr.57.3.703-724.1993

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  189 in total

1.  RNA polymerase II carboxy-terminal domain contributes to the response to multiple acidic activators in vitro.

Authors:  S M Liao; I C Taylor; R E Kingston; R A Young
Journal:  Genes Dev       Date:  1991-12       Impact factor: 11.361

2.  Relatedness of archaebacterial RNA polymerase core subunits to their eubacterial and eukaryotic equivalents.

Authors:  B Berghöfer; L Kröckel; C Körtner; M Truss; J Schallenberg; A Klein
Journal:  Nucleic Acids Res       Date:  1988-08-25       Impact factor: 16.971

3.  Mutations in RNA polymerase II enhance or suppress mutations in GAL4.

Authors:  L A Allison; C J Ingles
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

4.  Cloning and structure of a yeast gene encoding a general transcription initiation factor TFIID that binds to the TATA box.

Authors:  M Horikoshi; C K Wang; H Fujii; J A Cromlish; P A Weil; R G Roeder
Journal:  Nature       Date:  1989-09-28       Impact factor: 49.962

5.  A conjugation-specific gene (cnjC) from Tetrahymena encodes a protein homologous to yeast RNA polymerase subunits (RPB3, RPC40) and similar to a portion of the prokaryotic RNA polymerase alpha subunit (rpoA).

Authors:  D W Martindale
Journal:  Nucleic Acids Res       Date:  1990-05-25       Impact factor: 16.971

6.  Regulation of RNA polymerase II activity in alpha-amanitin-resistant CHO hybrid cells.

Authors:  A Guialis; B G Beatty; C J Ingles; M M Crerar
Journal:  Cell       Date:  1977-01       Impact factor: 41.582

7.  The RPC31 gene of Saccharomyces cerevisiae encodes a subunit of RNA polymerase C (III) with an acidic tail.

Authors:  C Mosrin; M Riva; M Beltrame; E Cassar; A Sentenac; P Thuriaux
Journal:  Mol Cell Biol       Date:  1990-09       Impact factor: 4.272

8.  Identification of phosphorylation sites in the repetitive carboxyl-terminal domain of the mouse RNA polymerase II largest subunit.

Authors:  J Zhang; J L Corden
Journal:  J Biol Chem       Date:  1991-02-05       Impact factor: 5.157

9.  Mutations in the second-largest subunit of Drosophila RNA polymerase II interact with Ubx.

Authors:  M A Mortin; R Zuerner; S Berger; B J Hamilton
Journal:  Genetics       Date:  1992-08       Impact factor: 4.562

10.  A unique structure at the carboxyl terminus of the largest subunit of eukaryotic RNA polymerase II.

Authors:  J L Corden; D L Cadena; J M Ahearn; M E Dahmus
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

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  56 in total

1.  Bacterial RNA polymerase subunit omega and eukaryotic RNA polymerase subunit RPB6 are sequence, structural, and functional homologs and promote RNA polymerase assembly.

Authors:  L Minakhin; S Bhagat; A Brunning; E A Campbell; S A Darst; R H Ebright; K Severinov
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-30       Impact factor: 11.205

2.  Escherichia coli RNA polymerase core and holoenzyme structures.

Authors:  R D Finn; E V Orlova; B Gowen; M Buck; M van Heel
Journal:  EMBO J       Date:  2000-12-15       Impact factor: 11.598

3.  Genetic evidence for selective degradation of RNA polymerase subunits by the 20S proteasome in Saccharomyces cerevisiae.

Authors:  S Nouraini; D Xu; S Nelson; M Lee; J D Friesen
Journal:  Nucleic Acids Res       Date:  1997-09-15       Impact factor: 16.971

Review 4.  5S rRNA gene arrangements in protists: a case of nonadaptive evolution.

Authors:  Guy Drouin; Corey Tsang
Journal:  J Mol Evol       Date:  2012-07-11       Impact factor: 2.395

Review 5.  Bacterial Transcription as a Target for Antibacterial Drug Development.

Authors:  Cong Ma; Xiao Yang; Peter J Lewis
Journal:  Microbiol Mol Biol Rev       Date:  2016-01-13       Impact factor: 11.056

6.  Why molecular chaperones buffer mutational damage: a case study with a yeast Hsp40/70 system.

Authors:  Joanna Bobula; Katarzyna Tomala; Elzbieta Jez; Dominika M Wloch; Rhona H Borts; Ryszard Korona
Journal:  Genetics       Date:  2006-07-18       Impact factor: 4.562

7.  Synthetic enhancement of a TFIIB defect by a mutation in SSU72, an essential yeast gene encoding a novel protein that affects transcription start site selection in vivo.

Authors:  Z W Sun; M Hampsey
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

8.  Many nonuniversal archaeal ribosomal proteins are found in conserved gene clusters.

Authors:  Jiachen Wang; Indrani Dasgupta; George E Fox
Journal:  Archaea       Date:  2009-04-28       Impact factor: 3.273

9.  Budding yeast RNA polymerases I and II employ parallel mechanisms of transcriptional termination.

Authors:  Junya Kawauchi; Hannah Mischo; Priscilla Braglia; Ana Rondon; Nick J Proudfoot
Journal:  Genes Dev       Date:  2008-04-15       Impact factor: 11.361

Review 10.  Molecular genetics of the RNA polymerase II general transcriptional machinery.

Authors:  M Hampsey
Journal:  Microbiol Mol Biol Rev       Date:  1998-06       Impact factor: 11.056

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