Targeting of AMSH to Endosomes Is Required for Epidermal Growth Factor Receptor Degradation
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 transpo...
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Veröffentlicht in: | The Journal of biological chemistry 2007-03, Vol.282 (13), p.9805-9812 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M611635200 |