| Literature DB >> 33571424 |
Heqiao Zhang1, Dong-Hua Chen2, Rayees U H Mattoo2, David A Bushnell2, Yannan Wang3, Chao Yuan3, Lin Wang3, Chunnian Wang3, Ralph E Davis2, Yan Nie4, Roger D Kornberg5.
Abstract
Mediator is a universal adaptor for transcription control. It serves as an interface between gene-specific activator or repressor proteins and the general RNA polymerase II (pol II) transcription machinery. Previous structural studies revealed a relatively small part of Mediator and none of the gene activator-binding regions. We have determined the cryo-EM structure of the Mediator at near-atomic resolution. The structure reveals almost all amino acid residues in ordered regions, including the major targets of activator proteins, the Tail module, and the Med1 subunit of the Middle module. Comparison of Mediator structures with and without pol II reveals conformational changes that propagate across the entire Mediator, from Head to Tail, coupling activator- and pol II-interacting regions.Entities:
Keywords: Mediator; activator; conformation change; cryo-EM; pol II; structure; transcription
Year: 2021 PMID: 33571424 DOI: 10.1016/j.molcel.2021.01.022
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970