| Literature DB >> 35051353 |
Chun Yang1, Rina Fujiwara2, Hee Jong Kim3, Pratik Basnet4, Yunye Zhu4, Jose J Gorbea Colón2, Stefan Steimle1, Benjamin A Garcia5, Craig D Kaplan4, Kenji Murakami6.
Abstract
Previous structural studies of the initiation-elongation transition of RNA polymerase II (pol II) transcription have relied on the use of synthetic oligonucleotides, often artificially discontinuous to capture pol II in the initiating state. Here, we report multiple structures of initiation complexes converted de novo from a 33-subunit yeast pre-initiation complex (PIC) through catalytic activities and subsequently stalled at different template positions. We determine that PICs in the initially transcribing complex (ITC) can synthesize a transcript of ∼26 nucleotides before transitioning to an elongation complex (EC) as determined by the loss of general transcription factors (GTFs). Unexpectedly, transition to an EC was greatly accelerated when an ITC encountered a downstream EC stalled at promoter proximal regions and resulted in a collided head-to-end dimeric EC complex. Our structural analysis reveals a dynamic state of TFIIH, the largest of GTFs, in PIC/ITC with distinct functional consequences at multiple steps on the pathway to elongation. Published by Elsevier Inc.Entities:
Keywords: RNA polymerase II; TFIIH; elongation complex; initially transcribing complex; pre-initiation complex; promoter escape; promoter opening; start-site scanning; transcription initiation; yeast
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Year: 2022 PMID: 35051353 PMCID: PMC8818039 DOI: 10.1016/j.molcel.2021.12.020
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970