Co-evolution of spliceosomal disassembly interologs: crowning J-protein component with moonlighting RNA-binding activity

Curr Genet. 2019 Apr;65(2):561-573. doi: 10.1007/s00294-018-0906-9. Epub 2018 Nov 22.

Abstract

Spliceosome disassembly is catalyzed by the NineTeen-related (NTR) complex, which is constituted by several proteins, including Cwc23, Ntr1, and Ppr43. Cwc23 is an essential J-protein in Saccharomyces cerevisiae that recruits Ntr1, an NTC-related G-patch protein, to the spliceosome. Ntr1 interacts with Prp43, a DExD/H box RNA helicase protein, which facilitates the disassembly of spliceosomal intermediates. The interaction between Ntr1 and Prp43 is conserved and crucial for the disassembly process. However, the J-protein component of this complex is not studied in other eukaryotes. In silico analysis supported by results of yeast complementation and two-hybrid studies suggests that while Prp43 is highly conserved, both Ntr1 and Cwc23 are co-evolving components of the disassembly triad. The J-domain of Cwc23, which is otherwise dispensable for its function, is highly conserved, whereas the functionally critical C-terminus has significantly diverged in Cwc23 orthologs. Some eukaryotic orthologs of Cwc23 contain a distinct RNA recognition motif at their C-terminus and are able to bind RNA in vitro. Based on the results presented in this study, we propose that RNA-binding activity in some eukaryotic orthologs of Cwc23 might provide additional functional diversity or robustness to the J-protein/Hsp70 machine in spliceosomal remodelling processes.

Keywords: Co-evolution; J-proteins; K. lactis; RRM; S. cerevisiae; S. pombe; Spliceosome.

MeSH terms

  • Biological Evolution*
  • Computational Biology / methods
  • Databases, Genetic
  • Models, Molecular
  • Multiprotein Complexes / metabolism
  • Protein Binding
  • Protein Conformation
  • RNA / chemistry
  • RNA / genetics*
  • RNA / metabolism*
  • RNA Splicing
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / chemistry
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Spliceosomes / metabolism*
  • Structure-Activity Relationship

Substances

  • Multiprotein Complexes
  • Saccharomyces cerevisiae Proteins
  • RNA