4.8 Article

Structure of promoter-bound TFIID and model of human pre-initiation complex assembly

期刊

NATURE
卷 531, 期 7596, 页码 604-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/nature17394

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资金

  1. National Energy Research Scientific Computing Center [DE-AC02-05CH11231]
  2. NIGMS [GM63072]
  3. Spanish Ministry of Economy and Competitiveness [BFU2013-44306P]
  4. NIGMS Molecular Biophysics Training Grant [GM008295]

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The general transcription factor IID (TFIID) plays a central role in the initiation of RNA polymerase II (Pol II)-dependent transcription by nucleating pre-initiation complex (PIC) assembly at the core promoter. TFIID comprises the TATA-binding protein (TBP) and 13 TBP-associated factors (TAF1-13), which specifically interact with a variety of core promoter DNA sequences. Here we present the structure of human TFIID in complex with TFIIA and core promoter DNA, determined by single-particle cryo-electron microscopy at sub-nanometre resolution. All core promoter elements are contacted by subunits of TFIID, with TAF1 and TAF2 mediating major interactions with the downstream promoter. TFIIA bridges the TBP-TATA complex with lobe B of TFIID. We also present the cryo-electron microscopy reconstruction of a fully assembled human TAF-less PIC. Superposition of common elements between the two structures provides novel insights into the general role of TFIID in promoter recognition, PIC assembly, and transcription initiation.

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