4.8 Article

Structural basis of RNA polymerase III transcription initiation

期刊

NATURE
卷 553, 期 7688, 页码 301-+

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NATURE PORTFOLIO
DOI: 10.1038/nature25441

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资金

  1. Marie Sklodowska-Curie Intra-European Fellowship (EU project) [655238]
  2. Cancer Research UK (CR-UK) [C12209/A16749]
  3. Biotechnology and Biological Sciences Research Council (BBSRC) New Investigator Award [BB/K014390/1]
  4. Cancer Research UK Programme Foundation (CR-UK) [C47547/A21536]
  5. Wellcome Trust Investigator Award [200818/Z/16/Z]
  6. BBSRC [BB/K014390/1] Funding Source: UKRI
  7. Wellcome Trust [200818/Z/16/Z] Funding Source: Wellcome Trust
  8. Marie Curie Actions (MSCA) [655238] Funding Source: Marie Curie Actions (MSCA)
  9. Biotechnology and Biological Sciences Research Council [BB/K014390/1] Funding Source: researchfish
  10. British Heart Foundation [PG/07/076/23480] Funding Source: researchfish
  11. Cancer Research UK [21536, 16749] Funding Source: researchfish
  12. Wellcome Trust [200818/Z/16/Z] Funding Source: researchfish

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RNA polymerase (Pol) III transcribes essential non-coding RNAs, including the entire pool of transfer RNAs, the 5S ribosomal RNA and the U6 spliceosomal RNA, and is often deregulated in cancer cells. The initiation of gene transcription by Pol III requires the activity of the transcription factor TFIIIB to form a transcriptionally active Pol III preinitiation complex (PIC). Here we present electron microscopy reconstructions of Pol III PICs at 3.4-4.0 angstrom and a reconstruction of unbound apo-Pol III at 3.1 angstrom. TFIIIB fully encircles the DNA and restructures Pol III. In particular, binding of the TFIIIB subunit Bdp1 rearranges the Pol III-specific subunits C37 and C34, thereby promoting DNA opening. The unwound DNA directly contacts both sides of the Pol III cleft. Topologically, the Pol III PIC resembles the Pol II PIC, whereas the Pol I PIC is more divergent. The structures presented unravel the molecular mechanisms underlying the first steps of Pol III transcription and also the general conserved mechanisms of gene transcription initiation.

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