Targeting of AMSH to endosomes is required for epidermal growth factor receptor degradation
- PMID: 17261583
- DOI: 10.1074/jbc.M611635200
Targeting of AMSH to endosomes is required for epidermal growth factor receptor degradation
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.
Similar articles
-
The MIT domain of UBPY constitutes a CHMP binding and endosomal localization signal required for efficient epidermal growth factor receptor degradation.J Biol Chem. 2007 Oct 19;282(42):30929-37. doi: 10.1074/jbc.M704009200. Epub 2007 Aug 21. J Biol Chem. 2007. PMID: 17711858
-
Interaction of AMSH with ESCRT-III and deubiquitination of endosomal cargo.J Biol Chem. 2006 Aug 11;281(32):23083-91. doi: 10.1074/jbc.M513803200. Epub 2006 Jun 7. J Biol Chem. 2006. PMID: 16760479
-
Activation of the endosome-associated ubiquitin isopeptidase AMSH by STAM, a component of the multivesicular body-sorting machinery.Curr Biol. 2006 Jan 24;16(2):160-5. doi: 10.1016/j.cub.2005.11.073. Curr Biol. 2006. PMID: 16431367
-
Down-regulation of epidermal growth factor receptor signalling within multivesicular bodies.Biochem Soc Trans. 2009 Feb;37(Pt 1):173-7. doi: 10.1042/BST0370173. Biochem Soc Trans. 2009. PMID: 19143625 Review.
-
Dissecting the role of His domain protein tyrosine phosphatase/PTPN23 and ESCRTs in sorting activated epidermal growth factor receptor to the multivesicular body.Biochem Soc Trans. 2018 Oct 19;46(5):1037-1046. doi: 10.1042/BST20170443. Epub 2018 Sep 6. Biochem Soc Trans. 2018. PMID: 30190330 Free PMC article. Review.
Cited by
-
Synergy between the ESCRT-III complex and Deltex defines a ligand-independent Notch signal.J Cell Biol. 2011 Dec 12;195(6):1005-15. doi: 10.1083/jcb.201104146. J Cell Biol. 2011. PMID: 22162134 Free PMC article.
-
Structural and thermodynamic comparison of the catalytic domain of AMSH and AMSH-LP: nearly identical fold but different stability.J Mol Biol. 2011 Oct 21;413(2):416-29. doi: 10.1016/j.jmb.2011.08.029. Epub 2011 Aug 24. J Mol Biol. 2011. PMID: 21888914 Free PMC article.
-
Structural basis for ESCRT-III CHMP3 recruitment of AMSH.Structure. 2011 Aug 10;19(8):1149-59. doi: 10.1016/j.str.2011.05.011. Structure. 2011. PMID: 21827950 Free PMC article.
-
Mechanisms of ErbB receptor negative regulation and relevance in cancer.Exp Cell Res. 2009 Feb 15;315(4):697-706. doi: 10.1016/j.yexcr.2008.07.022. Epub 2008 Jul 31. Exp Cell Res. 2009. PMID: 18706412 Free PMC article. Review.
-
How ubiquitin functions with ESCRTs.Traffic. 2011 Oct;12(10):1306-17. doi: 10.1111/j.1600-0854.2011.01242.x. Epub 2011 Jul 27. Traffic. 2011. PMID: 21722280 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous
