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Hrs and endocytic sorting of ubiquitinated membrane proteins

Journal

CELL STRUCTURE AND FUNCTION
Volume 27, Issue 6, Pages 403-408

Publisher

JAPAN SOC CELL BIOLOGY
DOI: 10.1247/csf.27.403

Keywords

endocytosis; Hrs; multivesicular body; ubiquitin; vacuolar protein sorting

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Endocytosed receptors are either recycled to the plasma membrane or trapped within intralumenal vesicles of multi-vesicular bodies for subsequent degradation in lysosomes. How the cell is able to sort receptors in endosomes has so far been largely unknown. The hepatocyte growth factor regulated tyrosine kinase substrate, Hrs, is an essential protein that has been implicated in cell signalling and intracellular membrane trafficking. Very recently, several reports have demonstrated a role for Hrs in endocytic sorting of ubiquitinated membrane proteins. Here, we review current knowledge about how Hrs recognises ubiquitinated cargo that is destined for lysosomal degradation, and how Hrs may act as a key regulator of the molecular machinery involved in receptor sorting and multivesicular body formation.

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