Abstract

Despite conservation of the signal recognition particle (SRP) from bacteria to man, computational approaches have failed to identify SRP components from genomes of many lower eukaryotes, raising the possibility that they have been lost or altered in those lineages. We report purification and analysis of SRP in the human pathogen Cryptococcus neoformans, providing the first description of SRP in basidiomycetous yeast. The C. neoformans SRP RNA displays a predicted structure in which the universally conserved helix 8 contains an unprecedented stem-loop insertion. Guided by this sequence, we computationally identified 152 SRP RNAs throughout the phylum Basidiomycota. This analysis revealed additional helix 8 alterations including single and double stem-loop insertions as well as loop diminutions affecting RNA structural elements that are otherwise conserved from bacteria to man. Strikingly, these SRP RNA features in Basidiomycota are accompanied by phylum-specific alterations in the RNA-binding domain of Srp54, the SRP protein subunit that directly interacts with helix 8. Our findings reveal unexpected fungal SRP diversity and suggest coevolution of the two most conserved SRP features—SRP RNA helix 8 and Srp54—in basidiomycetes. Because members of this phylum include important human and plant pathogens, these noncanonical features provide new targets for antifungal compound development.

Highlights

  • The signal recognition particle (SRP) is a ribonucleoprotein that directs protein sorting in all three domains of life [1], targeting substrates to the ER membrane in eukaryotes and to the plasma membrane in bacteria and archaea

  • The base of the Y constitutes the Alu domain: it binds to the SRP9/14 heterodimer and is responsible for translational arrest of SRP-bound ribosomes [3]

  • We constructed strains in which the endogenous Srp19 or Srp54 was tagged with a CBP-2xFLAG epitope

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Summary

Introduction

The signal recognition particle (SRP) is a ribonucleoprotein that directs protein sorting in all three domains of life [1], targeting substrates to the ER membrane in eukaryotes and to the plasma membrane in bacteria and archaea. The RNA is predicted to form an unusual secondary structure in which the Alu domain resembles that of ascomycetous fungi, whereas the S domain contains a dramatic stem-loop insertion within the universally conserved helix 8.

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