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

被引:64
作者
Ma, Yu May
Boucrot, Emmanuel
Villen, Judit
Affar, El Bachir
Gygi, Steven P.
Goettlinger, Heinrich G.
Kirchhausen, Tomas
机构
[1] Harvard Univ, Sch Med, CBR Inst Biomed Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
关键词
D O I
10.1074/jbc.M611635200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:9805 / 9812
页数:8
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