4.6 Article

Atomic modeling of the ITS2 ribosome assembly subcomplex from cryo-EM together with mass spectrometry-identified protein-protein crosslinks

Journal

PROTEIN SCIENCE
Volume 26, Issue 1, Pages 103-112

Publisher

WILEY
DOI: 10.1002/pro.3045

Keywords

cryo-EM; CXMS; ITS2; ribosome assembly; Cic1; Nop7; RIp7; Nop15; Nop53; crosslinking

Funding

  1. Ministry of Science and Technology of China [2013CB910404, 2016YFA0500700, 2014CB849800]
  2. National Natural Science Foundation of China [31422016, 31630087, 31470722, 21375010]
  3. NIH [R01GM028301]

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The assembly of ribosomal subunits starts in the nucleus, initiated by co-transcriptional folding of nascent ribosomal RNA (rRNA) transcripts and binding of ribosomal proteins and assembly factors. The internal transcribed spacer 2 (ITS2) is a precursor sequence to be processed from the intermediate 27S rRNA in the nucleoplasm; its removal is required for nuclear export of pre-60S particles. The proper processing of the ITS2 depends on multiple associated assembly factors and RNases. However, none of the structures of the known ITS2-binding factors is available. Here, we describe the modeling of the ITS2 subcomplex, including five assembly factors Cic1, Nop7, Nop15, Nop53, and RIp7, using a combination of cryo-electron microscopy and cross-linking of proteins coupled with mass spectrometry approaches. The resulting atomic models provide structural insights into their function in ribosome assembly, and establish a framework for further dissection of their molecular roles in ITS2 processing.

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