Structures of mammalian RNA polymerase II pre-initiation complexes

被引:62
作者
Aibara, Shintaro [1 ]
Schilbach, Sandra [1 ]
Cramer, Patrick [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Mol Biol, Gottingen, Germany
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
TRANSCRIPTION INITIATION; MECHANISM; TFIIH; VISUALIZATION; ARCHITECTURE; STEPS;
D O I
10.1038/s41586-021-03554-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The initiation of transcription is a focal point for the regulation of gene activity during mammalian cell differentiation and development. To initiate transcription, RNA polymerase II (Pol II) assembles with general transcription factors into a pre-initiation complex (PIC) that opens promoter DNA. Previous work provided the molecular architecture of the yeast(1-9) and human(10,11) PIC and a topological model for DNA opening by the general transcription factor TFIIH12-14. Here we report the high-resolution cryo-electron microscopy structure of PIC comprising human general factors and Sus scrofa domesticus Pol II, which is 99.9% identical to human Pol II. We determine the structures of PIC with closed and opened promoter DNA at 2.5-2.8 angstrom resolution, and resolve the structure of TFIIH at 2.9-4.0 angstrom resolution. We capture the TFIIH translocase XPB in the pre- and post-translocation states, and show that XPB induces and propagates a DNA twist to initiate the opening of DNA approximately 30 base pairs downstream of the TATA box. We also provide evidence that DNA opening occurs in two steps and leads to the detachment of TFIIH from the core PIC, which may stop DNA twisting and enable RNA chain initiation.
引用
收藏
页码:124 / +
页数:19
相关论文
共 47 条
  • [1] A versatile ligation-independent cloning method suitable for high-throughput expression screening applications
    Berrow, Nick S.
    Alderton, David
    Sainsbury, Sarah
    Nettleship, Joanne
    Assenberg, Rene
    Rahman, Nahid
    Stuart, David I.
    Owens, Raymond J.
    [J]. NUCLEIC ACIDS RESEARCH, 2007, 35 (06)
  • [2] TFIIE orchestrates the recruitment of the TFIIH kinase module at promoter before release during transcription
    Compe, Emmanuel
    Genes, Carlos M.
    Braun, Cathy
    Coin, Frederic
    Egly, Jean-Marc
    [J]. NATURE COMMUNICATIONS, 2019, 10 (1)
  • [3] Promoter Distortion and Opening in the RNA Polymerase II Cleft
    Dienemann, Christian
    Schwalb, Bjoern
    Schilbach, Sandra
    Cramer, Patrick
    [J]. MOLECULAR CELL, 2019, 73 (01) : 97 - +
  • [4] Features and development of Coot
    Emsley, P.
    Lohkamp, B.
    Scott, W. G.
    Cowtan, K.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2010, 66 : 486 - 501
  • [5] Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations
    Farnung, Lucas
    Ochmann, Moritz
    Cramer, Patrick
    [J]. ELIFE, 2020, 9 : 1 - 20
  • [6] Double-stranded DNA translocase activity of transcription factor TFIIH and the mechanism of RNA polymerase II open complex formation
    Fishburn, James
    Tomko, Eric
    Galburt, Eric
    Hahn, Steven
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (13) : 3961 - 3966
  • [7] DNA MELTING ON YEAST RNA POLYMERASE-II PROMOTERS
    GIARDINA, C
    LIS, JT
    [J]. SCIENCE, 1993, 261 (5122) : 759 - 762
  • [8] MacroBac: New Technologies for Robust and Efficient Large-Scale Production of Recombinant Multiprotein Complexes
    Gradia, Scott D.
    Ishida, Justin P.
    Tsai, Miaw-Sheue
    Jeans, Chris
    Tainer, John A.
    Fuss, Jill O.
    [J]. DNA REPAIR ENZYMES: STRUCTURE, BIOPHYSICS, AND MECHANISM, 2017, 592 : 1 - 26
  • [9] The complete structure of the human TFIIH core complex
    Greber, Basil J.
    Toso, Daniel B.
    Fang, Jie
    Nogales, Eva
    [J]. ELIFE, 2019, 8
  • [10] The cryo-electron microscopy structure of human transcription factor IIH
    Greber, Basil J.
    Nguyen, Thi Hoang Duong
    Fang, Jie
    Afonine, Pavel V.
    Adams, Paul D.
    Nogales, Eva
    [J]. NATURE, 2017, 549 (7672) : 414 - +