Arrestin-like proteins mediate ubiquitination and endocytosis of the yeast metal transporter Smf1

EMBO Rep. 2008 Dec;9(12):1216-21. doi: 10.1038/embor.2008.199. Epub 2008 Oct 24.

Abstract

Many plasma membrane proteins in yeast are ubiquitinated and endocytosed, but how they are recognized for modification has remained unknown. Here, we show that the manganese transporter Smf1 is endocytosed when cells are exposed to cadmium ions, that this endocytosis depends on Rsp5-dependent ubiquitination of specific lysines and that it also requires phosphorylation at nearby sites. This phosphorylation is, however, constitutive rather than stress-induced. Efficient ubiquitination requires Ecm21 or Csr2, two members of a family of arrestin-like yeast proteins that contain several PY motifs and bind to Rsp5. Ecm21 also binds to phosphorylated Smf1, providing a link between Rsp5 and its substrate. PY motif-containing arrestin-like proteins are found in many species, including humans, and might have a general role as ubiquitin ligase adaptors.

MeSH terms

  • Arrestin / metabolism*
  • Cadmium / toxicity
  • Cation Transport Proteins / metabolism*
  • Cross-Linking Reagents
  • Endocytosis*
  • Endosomal Sorting Complexes Required for Transport
  • Green Fluorescent Proteins
  • Lysine
  • Phosphorylation
  • Protein Binding
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae / cytology*
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Ubiquitin-Protein Ligase Complexes
  • Ubiquitination*

Substances

  • Arrestin
  • Cation Transport Proteins
  • Cross-Linking Reagents
  • Ecm21 protein, S cerevisiae
  • Endosomal Sorting Complexes Required for Transport
  • Recombinant Fusion Proteins
  • SMF1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Cadmium
  • Green Fluorescent Proteins
  • Ubiquitin-Protein Ligase Complexes
  • RSP5 protein, S cerevisiae
  • Lysine