Targeting of AMSH to endosomes is required for epidermal growth factor receptor degradation

J Biol Chem. 2007 Mar 30;282(13):9805-9812. doi: 10.1074/jbc.M611635200. Epub 2007 Jan 29.

Abstract

To reach the lysosomes, down-regulated receptors such as the epidermal growth factor receptor must first be sorted into internal vesicles of late endosomes (multivesicular bodies), a ubiquitin-dependent event that requires the coordinated function of the endosome sorting complex required for transport (ESCRT) proteins. Here we report that CHMP3, an ESCRT-III complex component, and associated molecule of SH3 domain of STAM (AMSH), a deubiquitinating enzyme, interact with each other in cells. A dominant-negative version of CHMP3, which specifically prevents targeting of AMSH to endosomes, inhibits degradation but not internalization of EGFR, suggesting that endosomal AMSH is a functional component of the multivesicular body pathway.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • Endosomal Sorting Complexes Required for Transport
  • Endosomes / enzymology*
  • Endosomes / metabolism
  • ErbB Receptors / metabolism*
  • HeLa Cells
  • Humans
  • Molecular Sequence Data
  • Nerve Tissue Proteins / metabolism
  • Protein Transport / physiology
  • Signal Transduction / physiology
  • Ubiquitin Thiolesterase / metabolism*

Substances

  • CHMP3 protein, human
  • Endosomal Sorting Complexes Required for Transport
  • Nerve Tissue Proteins
  • STAMBP protein, human
  • ErbB Receptors
  • Ubiquitin Thiolesterase