4.8 Article

Structural basis of initial RNA polymerase II transcription

Journal

EMBO JOURNAL
Volume 30, Issue 23, Pages 4755-4763

Publisher

WILEY
DOI: 10.1038/emboj.2011.396

Keywords

gene transcription; NTP binding; RNA polymerase; transcription initiation

Funding

  1. Deutsche Forschungsgemeinschaft [SFB646, TR5, FOR1068, SFB960]
  2. NIM
  3. European Molecular Biology Organization (EMBO)
  4. European Research Council
  5. LMU
  6. Jung-Stiftung

Ask authors/readers for more resources

During transcription initiation by RNA polymerase (Pol) II, a transient open promoter complex (OC) is converted to an initially transcribing complex (ITC) containing short RNAs, and to a stable elongation complex (EC). We report structures of a Pol II-DNA complex mimicking part of the OC, and of complexes representing minimal ITCs with 2, 4, 5, 6, and 7 nucleotide (nt) RNAs, with and without a non-hydrolyzable nucleoside triphosphate (NTP) in the insertion site +1. The partial OC structure reveals that Pol II positions the melted template strand opposite the active site. The ITC-mimicking structures show that two invariant lysine residues anchor the 3'-proximal phosphate of short RNAs. Short DNA-RNA hybrids adopt a tilted conformation that excludes the +1 template nt from the active site. NTP binding induces complete DNA translocation and the standard hybrid conformation. Conserved NTP contacts indicate a universal mechanism of NTP selection. The essential residue Q1078 in the closed trigger loop binds the NTP 2'-OH group, explaining how the trigger loop couples catalysis to NTP selection, suppressing dNTP binding and DNA synthesis. The EMBO Journal (2011) 30, 4755-4763. doi:10.1038/emboj.2011.396; Published online 4 November 2011

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available