Litcius/Paper detail

O-GlcNAcylation regulates epidermal growth factor receptor intracellular trafficking and signaling

Liming Wu, Yaxian Cheng, Didi Geng, Zhiya Fan, Bingyi Lin, Qiang Zhu, Jingchao Li, Weijie Qin, Wen Yi

2022Proceedings of the National Academy of Sciences60 citationsDOIOpen Access PDF

Abstract

SignificanceEpidermal growth factor receptor (EGFR) is one of the most important membrane receptors that transduce growth signals into cells to sustain cell growth, proliferation, and survival. EGFR signal termination is initiated by EGFR internalization, followed by trafficking through endosomes, and degradation in lysosomes. How this process is regulated is still poorly understood. Here, we show that hepatocyte growth factor regulated tyrosine kinase substrate (HGS), a key protein in the EGFR trafficking pathway, is dynamically modified by a single sugar N-acetylglucosamine. This modification inhibits EGFR trafficking from endosomes to lysosomes, leading to the accumulation of EGFR and prolonged signaling. This study provides an important insight into diseases with aberrant growth factor signaling, such as cancer, obesity, and diabetes.

Topics & Concepts

EndosomeCell biologyEpidermal growth factor receptorEpidermal growth factorInternalizationSignal transductionERBB3Growth factor receptorGrowth factorHepatocyte Growth Factor ReceptorBiologyProtein kinase BReceptor tyrosine kinaseIntracellularHepatocyte growth factorChemistryReceptorBiochemistryC-MetGlycosylation and Glycoproteins ResearchProtein Tyrosine PhosphatasesUbiquitin and proteasome pathways