Literature DB >> 3304659

Functional redundancy and structural polymorphism in the large subunit of RNA polymerase II.

M Nonet, D Sweetser, R A Young.   

Abstract

The RNA polymerase II large subunit contains tandem copies of the sequence Pro Thr Ser Pro Ser Tyr Ser at its carboxyl terminus, the number of which varies from 26 in yeast to 52 in mice. Our results indicate that the heptapeptide repeat sequence is unique and essential to RNA polymerase II. We have determined that a portion of the heptapeptide repeat domain is essential for viability by constructing and analyzing unidirectional deletions of the carboxy-terminal coding sequence in yeast. Cells containing an RNA polymerase II large subunit with less than 10 complete heptapeptide repeats are inviable, those containing 10-12 complete repeats are conditionally viable, and those with 13 or more complete repeats are unconditionally viable. The inviable deletion mutants studied here have truncated RNA polymerase subunits that are stable, but functionally deficient. Finally, the number of repeat units is polymorphic in wild-type yeast strains. These results have implications for the function of this unusual sequence in transcription.

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Year:  1987        PMID: 3304659     DOI: 10.1016/0092-8674(87)90517-4

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


  134 in total

1.  Topological localization of the carboxyl-terminal domain of RNA polymerase II in the initiation complex.

Authors:  M Douziech; D Forget; J Greenblatt; B Coulombe
Journal:  J Biol Chem       Date:  1999-07-09       Impact factor: 5.157

2.  Evolution of the RNA polymerase II C-terminal domain.

Authors:  John W Stiller; Benjamin D Hall
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-23       Impact factor: 11.205

3.  Requirements of the RNA polymerase II C-terminal domain for reconstituting pre-mRNA 3' cleavage.

Authors:  Kevin Ryan; Kanneganti G K Murthy; Syuzo Kaneko; James L Manley
Journal:  Mol Cell Biol       Date:  2002-03       Impact factor: 4.272

4.  An initiation element in the yeast CUP1 promoter is recognized by RNA polymerase II in the absence of TATA box-binding protein if the DNA is negatively supercoiled.

Authors:  B P Leblanc; C J Benham; D J Clark
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

Review 5.  RNA polymerase II carboxy-terminal domain kinases: emerging clues to their function.

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

6.  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

7.  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

8.  A yeast heterogeneous nuclear ribonucleoprotein complex associated with RNA polymerase II.

Authors:  N K Conrad; S M Wilson; E J Steinmetz; M Patturajan; D A Brow; M S Swanson; J L Corden
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

9.  A 10 residue motif at the C-terminus of the RNA pol II CTD is required for transcription, splicing and 3' end processing.

Authors:  Nova Fong; Gregory Bird; Marc Vigneron; David L Bentley
Journal:  EMBO J       Date:  2003-08-15       Impact factor: 11.598

10.  Activated transcription independent of the RNA polymerase II holoenzyme in budding yeast.

Authors:  J B McNeil; H Agah; D Bentley
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

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