Literature DB >> 3896517

Extensive homology among the largest subunits of eukaryotic and prokaryotic RNA polymerases.

L A Allison, M Moyle, M Shales, C J Ingles.   

Abstract

We have determined the nucleotide sequence of two yeast RNA polymerase genes, RPO21 and RPO31, which encode the largest subunits of RNA polymerases II and III, respectively. The RPO21 and RPO31 sequences are homologous to each other, to the sequence of the largest subunit of E. coli RNA polymerase, and to sequences in the putative DNA-binding domain of E. coli DNA polymerase I. RPO21 has an unusual heptapeptide sequence tandemly repeated 26 times at its C-terminus; this sequence is conserved in the RNA polymerase II of higher eukaryotes and may play an important role in polymerase II-mediated transcription. Since eukaryotic and prokaryotic RNA polymerases appear to have evolved from a common ancestral polymerase, other features of the transcription process may also be evolutionarily conserved.

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Year:  1985        PMID: 3896517     DOI: 10.1016/0092-8674(85)90117-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  244 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.  Use of DNA, RNA, and chimeric templates by a viral RNA-dependent RNA polymerase: evolutionary implications for the transition from the RNA to the DNA world.

Authors:  R W Siegel; L Bellon; L Beigelman; C C Kao
Journal:  J Virol       Date:  1999-08       Impact factor: 5.103

3.  Transcription in archaea.

Authors:  N C Kyrpides; C A Ouzounis
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-20       Impact factor: 11.205

4.  A zinc-binding site in the largest subunit of DNA-dependent RNA polymerase is involved in enzyme assembly.

Authors:  D Markov; T Naryshkina; A Mustaev; K Severinov
Journal:  Genes Dev       Date:  1999-09-15       Impact factor: 11.361

5.  Localization of Escherichia coli rpoC mutations that affect RNA polymerase assembly and activity at high temperature.

Authors:  E C Nedea; D Markov; T Naryshkina; K Severinov
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

6.  Structure-based analysis of RNA polymerase function: the largest subunit's rudder contributes critically to elongation complex stability and is not involved in the maintenance of RNA-DNA hybrid length.

Authors:  Konstantin Kuznedelov; Nataliya Korzheva; Arkady Mustaev; Konstantin Severinov
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

Review 7.  RNA polymerase II carboxy-terminal domain kinases: emerging clues to their function.

Authors:  Gregory Prelich
Journal:  Eukaryot Cell       Date:  2002-04

8.  Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs.

Authors:  Manabu Nakayama; Reiko Kikuno; Osamu Ohara
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

9.  Synonymous rates at the RpII215 gene of Drosophila: variation among species and across the coding region.

Authors:  A Llopart; M Aguadé
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

10.  Bur1 kinase is required for efficient transcription elongation by RNA polymerase II.

Authors:  Michael-Christopher Keogh; Vladimir Podolny; Stephen Buratowski
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

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