Literature DB >> 2406567

Conditional mutations occur predominantly in highly conserved residues of RNA polymerase II subunits.

C Scafe1, C Martin, M Nonet, S Podos, S Okamura, R A Young.   

Abstract

Conditional mutations in the Saccharomyces cerevisiae RNA polymerase II large subunit, RPB1, were obtained by introducing a mutagenized RPB1 plasmid into yeast cells, selecting for loss of the wild-type RPB1 gene, and screening the cells for heat or cold sensitivity. Sequence analysis of 10 conditional RPB1 mutations and 10 conditional RPB2 mutations revealed that the amino acid residues altered by these distinct mutations are nearly always invariant among eucaryotic RPB1 and RPB2 homologs. These results suggest that RNA polymerase mutants might be obtained in other eucaryotic organisms by alteration of these invariant residues.

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Year:  1990        PMID: 2406567      PMCID: PMC361019          DOI: 10.1128/mcb.10.3.1270-1275.1990

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  26 in total

Review 1.  Genetics of bacterial RNA polymerases.

Authors:  T Yura; A Ishihama
Journal:  Annu Rev Genet       Date:  1979       Impact factor: 16.830

2.  A suppressor of a HIS4 transcriptional defect encodes a protein with homology to the catalytic subunit of protein phosphatases.

Authors:  K T Arndt; C A Styles; G R Fink
Journal:  Cell       Date:  1989-02-24       Impact factor: 41.582

3.  RNA polymerase II mutants defective in transcription of a subset of genes.

Authors:  C Scafe; M Nonet; R A Young
Journal:  Mol Cell Biol       Date:  1990-03       Impact factor: 4.272

4.  Conservation of a DNA-binding site in the largest subunit of eukaryotic RNA polymerase II.

Authors:  S B Carroll; B D Stollar
Journal:  J Mol Biol       Date:  1983-11-05       Impact factor: 5.469

5.  Molecular cloning and sequencing of ama-1, the gene encoding the largest subunit of Caenorhabditis elegans RNA polymerase II.

Authors:  D M Bird; D L Riddle
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

6.  Probes of eukaryotic DNA-dependent RNA polymerase II-I. Binding of 9-beta-D-arabinofuranosyl-6-mercaptopurine to the elongation subsite.

Authors:  J M Cho; A P Kimball
Journal:  Biochem Pharmacol       Date:  1982-08-15       Impact factor: 5.858

7.  Analysis of the gene encoding the largest subunit of RNA polymerase II in Drosophila.

Authors:  R S Jokerst; J R Weeks; W A Zehring; A L Greenleaf
Journal:  Mol Gen Genet       Date:  1989-01

8.  Intragenic and extragenic suppressors of mutations in the heptapeptide repeat domain of Saccharomyces cerevisiae RNA polymerase II.

Authors:  M L Nonet; R A Young
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

9.  A Caenorhabditis elegans RNA polymerase II gene, ama-1 IV, and nearby essential genes.

Authors:  T M Rogalski; D L Riddle
Journal:  Genetics       Date:  1988-01       Impact factor: 4.562

10.  Yeast RNA polymerase II genes: isolation with antibody probes.

Authors:  R A Young; R W Davis
Journal:  Science       Date:  1983-11-18       Impact factor: 47.728

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  51 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.  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

3.  The REG1 gene product is required for repression of INO1 and other inositol-sensitive upstream activating sequence-containing genes of yeast.

Authors:  Q Ouyang; M Ruiz-Noriega; S A Henry
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

4.  Effect of mutations in a zinc-binding domain of yeast RNA polymerase C (III) on enzyme function and subunit association.

Authors:  M Werner; S Hermann-Le Denmat; I Treich; A Sentenac; P Thuriaux
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

5.  The conserved foot domain of RNA pol II associates with proteins involved in transcriptional initiation and/or early elongation.

Authors:  M Carmen García-López; Vicent Pelechano; M Carmen Mirón-García; Ana I Garrido-Godino; Alicia García; Olga Calvo; Michel Werner; José E Pérez-Ortín; Francisco Navarro
Journal:  Genetics       Date:  2011-09-27       Impact factor: 4.562

6.  Kin28, the TFIIH-associated carboxy-terminal domain kinase, facilitates the recruitment of mRNA processing machinery to RNA polymerase II.

Authors:  C R Rodriguez; E J Cho; M C Keogh; C L Moore; A L Greenleaf; S Buratowski
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

7.  Evidence that the transcription elongation function of Rpb9 is involved in transcription-coupled DNA repair in Saccharomyces cerevisiae.

Authors:  Shisheng Li; Baojin Ding; Runqiang Chen; Christine Ruggiero; Xuefeng Chen
Journal:  Mol Cell Biol       Date:  2006-10-09       Impact factor: 4.272

8.  Mutations in the three largest subunits of yeast RNA polymerase II that affect enzyme assembly.

Authors:  P A Kolodziej; R A Young
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

Review 9.  Structural perspective on mutations affecting the function of multisubunit RNA polymerases.

Authors:  Vincent Trinh; Marie-France Langelier; Jacques Archambault; Benoit Coulombe
Journal:  Microbiol Mol Biol Rev       Date:  2006-03       Impact factor: 11.056

Review 10.  Tailored tails and transcription initiation: the carboxyl terminal domain of RNA polymerase II.

Authors:  D M Chao; R A Young
Journal:  Gene Expr       Date:  1991-04
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