Proteomic analysis of human Nop56p-associated pre-ribosomal ribonucleoprotein complexes. Possible link between Nop56p and the nucleolar protein treacle responsible for Treacher Collins syndrome

J Biol Chem. 2003 Sep 5;278(36):34309-19. doi: 10.1074/jbc.M304304200. Epub 2003 May 30.

Abstract

Nop56p is a component of the box C/D small nucleolar ribonucleoprotein complexes that direct 2'-O-methylation of pre-rRNA during its maturation. Genetic analyses in yeast have shown that Nop56p plays important roles in the early steps of pre-rRNA processing. However, its precise function remains elusive, especially in higher eukaryotes. Here we describe the proteomic characterization of human Nop56p (hNop56p)-associated pre-ribosomal ribonucleoprotein complexes. Mass spectrometric analysis of purified pre-ribosomal ribonucleoprotein complexes identified 61 ribosomal proteins, 16 trans-acting factors probably involved in ribosome biogenesis, and 29 proteins whose function in ribosome biogenesis is unknown. Identification of pre-rRNA species within hNop56p-associated pre-ribosomal ribonucleoprotein complexes, coupled with the known functions of yeast orthologs of the probable trans-acting factors identified in human, demonstrated that hNop56p functions in the early to middle stages of 60 S subunit synthesis in human cells. Interestingly, the nucleolar phosphoprotein treacle, which is responsible for the craniofacial disorder associated with Treacher Collins syndrome, was found to be a constituent of hNop56p-associated pre-rRNP complexes. The association of hNop56p and treacle within the complexes was independent of rRNA integrity, indicating a direct interaction. In addition, the protein compositions of the treacle-associated and hNop56p-associated pre-ribosomal ribonucleoprotein complexes were very similar, suggesting functional similarities between these two complexes with respect to ribosome biogenesis in human cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Blotting, Northern
  • Cell Line
  • Cell Nucleolus / metabolism
  • Cell Nucleus / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Epitopes
  • Humans
  • Immunohistochemistry
  • Mandibulofacial Dysostosis / metabolism
  • Mass Spectrometry
  • Models, Genetic
  • Nuclear Proteins / chemistry*
  • Nuclear Proteins / metabolism*
  • Phosphoproteins / metabolism
  • Precipitin Tests
  • Protein Binding
  • Protein Structure, Tertiary
  • Proteome / metabolism
  • RNA, Ribosomal / chemistry*
  • RNA, Ribosomal / metabolism
  • Ribonucleases / metabolism
  • Ribonucleoproteins / metabolism*
  • Ribosomes / metabolism*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Transfection

Substances

  • Epitopes
  • NOP56 protein, human
  • Nuclear Proteins
  • Phosphoproteins
  • Proteome
  • RNA, Ribosomal
  • Ribonucleoproteins
  • TCOF1 protein, human
  • Ribonucleases