Literature DB >> 12912924

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

Nova Fong1, Gregory Bird, Marc Vigneron, David L Bentley.   

Abstract

The RNA polymerase II C-terminal heptad repeat domain (CTD) is essential for normal transcription and co-transcriptional processing of mRNA precursors. The mammalian CTD comprises 52 heptads whose consensus, YSPTSPS, is conserved throughout eukaryotes, followed by a 10 amino acid C-terminal sequence that is conserved only among vertebrates. Here we show that surprisingly, the heptad repeats are not sufficient to support efficient transcription, pre-mRNA processing or full cell viability. In addition to the heptads, the 10 amino acid C-terminal motif is essential for high level transcription, splicing and poly(A) site cleavage. Efficient mRNA synthesis from a transiently transfected reporter gene required the C-terminal motif plus between 16 and 25 heptad repeats from either the N- or C-terminal half of the CTD. Twenty-seven consensus heptads plus the C-terminal motif also supported efficient mRNA synthesis but not cell viability.

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Year:  2003        PMID: 12912924      PMCID: PMC175786          DOI: 10.1093/emboj/cdg396

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  33 in total

1.  RNA polymerase II targets pre-mRNA splicing factors to transcription sites in vivo.

Authors:  T Misteli; D L Spector
Journal:  Mol Cell       Date:  1999-06       Impact factor: 17.970

Review 2.  RNA polymerase II and the integration of nuclear events.

Authors:  Y Hirose; J L Manley
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

Review 3.  Transcription of eukaryotic protein-coding genes.

Authors:  T I Lee; R A Young
Journal:  Annu Rev Genet       Date:  2000       Impact factor: 16.830

4.  Capping, splicing, and 3' processing are independently stimulated by RNA polymerase II: different functions for different segments of the CTD.

Authors:  N Fong; D L Bentley
Journal:  Genes Dev       Date:  2001-07-15       Impact factor: 11.361

5.  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

6.  Structural basis of transcription: RNA polymerase II at 2.8 angstrom resolution.

Authors:  P Cramer; D A Bushnell; R D Kornberg
Journal:  Science       Date:  2001-04-19       Impact factor: 47.728

7.  Functional interaction of yeast pre-mRNA 3' end processing factors with RNA polymerase II.

Authors:  Donny D Licatalosi; Gabrielle Geiger; Michelle Minet; Stephanie Schroeder; Kate Cilli; J Bryan McNeil; David L Bentley
Journal:  Mol Cell       Date:  2002-05       Impact factor: 17.970

Review 8.  The mRNA assembly line: transcription and processing machines in the same factory.

Authors:  David Bentley
Journal:  Curr Opin Cell Biol       Date:  2002-06       Impact factor: 8.382

9.  A human RNA polymerase II-containing complex associated with factors necessary for spliceosome assembly.

Authors:  Francois Robert; Marco Blanchette; Olivier Maes; Benoit Chabot; Benoit Coulombe
Journal:  J Biol Chem       Date:  2001-12-31       Impact factor: 5.157

10.  Human CRSP interacts with RNA polymerase II CTD and adopts a specific CTD-bound conformation.

Authors:  Anders M Näär; Dylan J Taatjes; Weiguo Zhai; Eva Nogales; Robert Tjian
Journal:  Genes Dev       Date:  2002-06-01       Impact factor: 11.361

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  26 in total

Review 1.  Multiple links between transcription and splicing.

Authors:  Alberto R Kornblihtt; Manuel de la Mata; Juan Pablo Fededa; Manuel J Munoz; Guadalupe Nogues
Journal:  RNA       Date:  2004-10       Impact factor: 4.942

2.  Analysis of the requirement for RNA polymerase II CTD heptapeptide repeats in pre-mRNA splicing and 3'-end cleavage.

Authors:  Emanuel Rosonina; Benjamin J Blencowe
Journal:  RNA       Date:  2004-04       Impact factor: 4.942

3.  Transcription and splicing: when the twain meet.

Authors:  Yehuda Brody; Yaron Shav-Tal
Journal:  Transcription       Date:  2011 Sep-Oct

4.  Prolonged α-amanitin treatment of cells for studying mutated polymerases causes degradation of DSIF160 and other proteins.

Authors:  David C Tsao; Noh Jin Park; Anita Nag; Harold G Martinson
Journal:  RNA       Date:  2011-12-22       Impact factor: 4.942

5.  Chromatin density and splicing destiny: on the cross-talk between chromatin structure and splicing.

Authors:  Schraga Schwartz; Gil Ast
Journal:  EMBO J       Date:  2010-04-20       Impact factor: 11.598

6.  Role of the mammalian RNA polymerase II C-terminal domain (CTD) nonconsensus repeats in CTD stability and cell proliferation.

Authors:  Rob D Chapman; Marcus Conrad; Dirk Eick
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

7.  The conserved AAUAAA hexamer of the poly(A) signal can act alone to trigger a stable decrease in RNA polymerase II transcription velocity.

Authors:  Anita Nag; Kazim Narsinh; Amir Kazerouninia; Harold G Martinson
Journal:  RNA       Date:  2006-06-14       Impact factor: 4.942

8.  The C-terminal domain of RNA Pol II helps ensure that editing precedes splicing of the GluR-B transcript.

Authors:  Kicki Ryman; Nova Fong; Eva Bratt; David L Bentley; Marie Ohman
Journal:  RNA       Date:  2007-05-24       Impact factor: 4.942

9.  The Iws1:Spt6:CTD complex controls cotranscriptional mRNA biosynthesis and HYPB/Setd2-mediated histone H3K36 methylation.

Authors:  Sunnie M Yoh; Joseph S Lucas; Katherine A Jones
Journal:  Genes Dev       Date:  2008-12-15       Impact factor: 11.361

10.  Targeting tat inhibitors in the assembly of human immunodeficiency virus type 1 transcription complexes.

Authors:  Iván D'Orso; Jocelyn R Grunwell; Robert L Nakamura; Chandreyee Das; Alan D Frankel
Journal:  J Virol       Date:  2008-07-30       Impact factor: 5.103

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