4.7 Article

The complete structure of the small-subunit processome

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 24, Issue 11, Pages 944-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.3472

Keywords

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Funding

  1. EMBO [ALTF 51-2014]
  2. Swiss National Science Foundation [155515]
  3. Natural Sciences and Engineering Research Council of Canada (NSERC)
  4. Robertson Foundation
  5. Alfred P. Sloan Foundation
  6. Irma T. Hirschl Trust
  7. Alexandrine and Alexander L. Sinsheimer Fund
  8. Human Frontier Science Program Development Award
  9. NIH [1DP2GM123459]
  10. National Institute of Health [P41GM103314, P41GM109824]

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The small-subunit processome represents the earliest stable precursor of the eukaryotic small ribosomal subunit. Here we present the cryo-EM structure of the Saccharomyces cerevisiae small-subunit processome at an overall resolution of 3.8 angstrom, which provides an essentially complete near-atomic model of this assembly. In this nucleolar superstructure, 51 ribosome-assembly factors and two RNAs encapsulate the 18S rRNA precursor and 15 ribosomal proteins in a state that precedes pre-rRNA cleavage at site A1. Extended flexible proteins are employed to connect distant sites in this particle. Molecular mimicry and steric hindrance, as well as protein-and RNA-mediated RNA remodeling, are used in a concerted fashion to prevent the premature formation of the central pseudoknot and its surrounding elements within the small ribosomal subunit.

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