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Journal Article

Dynamic architecture of a minimal RNA polymerase II open promoter complex

MPS-Authors
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Cramer,  P.
Department of Molecular Biology, MPI for Biophysical Chemistry, Max Planck Society;

Fulltext (public)

1933169.pdf
(Publisher version), 3MB

Supplementary Material (public)

1933169-Suppl.pdf
(Supplementary material), 3MB

Citation

Treutlein, B., Muschielok, A., Andrecka, J., Jawhari, A., Buchen, C., Kostrewa, D., et al. (2012). Dynamic architecture of a minimal RNA polymerase II open promoter complex. Molecular Cell, 46(2), 136-146. doi:10.1016/j.molcel.2012.02.008.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0015-4547-C
Abstract
The open promoter complex (OC) is a central intermediate during transcription initiation that contains a DNA bubble. Here, we employ singlemolecule Fo¨ rster resonance energy transfer experiments and Nano-Positioning System analysis to determine the three-dimensional architecture of a minimal OC consisting of promoter DNA, including a TATA box and an 11-nucleotide mismatched region around the transcription start site, TATA box-binding protein (TBP), RNA polymerase (Pol) II, and general transcription factor (TF)IIB and TFIIF. In this minimal OC, TATA-DNA and TBP reside above the Pol II cleft between clamp and protrusion domains. DownstreamDNA is dynamically loaded into and unloaded from the Pol II cleft at a timescale of seconds. The TFIIB core domain is displaced from the Pol II wall, where it is located in the closed promoter complex. These results reveal large overall structural changes during the initiation-elongation transition, which are apparently accommodated by the intrinsic flexibility of TFIIB.