scholarly journals YXXM Motifs in the PDGF-β Receptor Serve Dual Roles as Phosphoinositide 3-Kinase Binding Motifs and Tyrosine-based Endocytic Sorting Signals

2003 ◽  
Vol 278 (42) ◽  
pp. 40425-40428 ◽  
Author(s):  
Haiyan Wu ◽  
David A. Windmiller ◽  
Ling Wang ◽  
Jonathan M. Backer
eLife ◽  
2014 ◽  
Vol 3 ◽  
Author(s):  
Shen Yue ◽  
Liu-Ya Tang ◽  
Ying Tang ◽  
Yi Tang ◽  
Qiu-Hong Shen ◽  
...  

Cell surface reception of Sonic hedgehog (Shh) must ensure that the graded morphogenic signal is interpreted accordingly in neighboring cells to specify tissue patterns during development. Here, we report endocytic sorting signals for the receptor Patched1 (Ptch1), comprising two ‘PPXY’ motifs, that direct it to degradation in lysosomes. These signals are recognized by two HECT-domain ubiquitin E3 ligases, Smurf1 and Smurf2, which are induced by Shh and become enriched in Caveolin-1 lipid rafts in association with Ptch1. Smurf-mediated endocytic turnover of Ptch1 is essential for its clearance from the primary cilium and pathway activation. Removal of both Smurfs completely abolishes the ability of Shh to sustain the proliferation of postnatal granule cell precursors in the cerebellum. These findings reveal a novel step in the Shh pathway activation as part of the Ptch1 negative feedback loop that precisely controls the signaling output in response to Shh gradient signal.


2007 ◽  
Vol 39 (5) ◽  
pp. 329-332 ◽  
Author(s):  
Nima Sharifi ◽  
Robert J Lechleider ◽  
William L Farrar

AbstractThe transforming growth factor-β (TGF-β) pathway plays dual roles in cancer, inhibiting epithelial cell growth under normal physiologic conditions, but promoting invasion and metastasis once growth inhibitory responses are lost. Two recent papers show that TGF-β receptor III is the most common TGF-β pathway component downregulated in prostate cancer. Here, we discuss the implications of these findings and what it may mean about the biology of this disease.


Oncogene ◽  
2013 ◽  
Vol 33 (15) ◽  
pp. 1934-1944 ◽  
Author(s):  
S Laval ◽  
H Laklai ◽  
M Fanjul ◽  
M Pucelle ◽  
H Laurell ◽  
...  

1997 ◽  
Vol 16 (9) ◽  
pp. 2240-2250 ◽  
Author(s):  
Iris Rapoport ◽  
Masaya Miyazaki ◽  
Werner Boll ◽  
Brian Duckworth ◽  
Lewis C. Cantley ◽  
...  

2001 ◽  
Vol 354 (3) ◽  
pp. 561-572 ◽  
Author(s):  
Wei HU ◽  
Marybeth HOWARD ◽  
Gergely L. LUKACS

The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-dependent protein kinase (PKA)-activated chloride channel that is localized to the plasma membrane and endosomal compartment. Endosomal targeting of CFTR is attributed to the Tyr1424-based internalization signal, identified in the C-terminal tail of the channel. Mutation of the Tyr1424 residue could partly inhibit the endocytosis of CFTR and its association with the adapter protein AP-2. To reveal additional endosomal targeting signals, site-directed mutagenesis of both a chimaera, composed of a truncated form of interleukin 2 receptor α chain (TacT) and the C-terminal tail of CFTR (Ct), and the full-length CFTR was performed. Morphological and functional assays revealed the presence of multiple internalization motifs at the C-terminus, consisting of a phenylalanine-based motif (Phe1413) and a bipartite endocytic signal, comprising a tyrosine (Tyr1424) and a di-Leu-based (Leu1430-Leu) motif. Whereas the replacement of any one of the three internalization motifs with alanine prevented the endocytosis of the TacT–Ct chimaera, mutagenesis of Phe1413-Leu impaired the biosynthetic processing of CFTR, indicating that Phe1413 is indispensable for the native structure of CFTR. In contrast, replacement of Leu1430-Leu- and Tyr1424-based signals with alanine increased the cell-surface density of both the chimaeras and CFTR in an additive manner. These results suggest that the internalization of CFTR is regulated by multiple endocytic sorting signals.


2008 ◽  
Vol 410 (1) ◽  
pp. 1-17 ◽  
Author(s):  
Jonathan M. Backer

The Class III PI3K (phosphoinositide 3-kinase), Vps34 (vacuolar protein sorting 34), was first described as a component of the vacuolar sorting system in Saccharomyces cerevisiae and is the sole PI3K in yeast. The homologue in mammalian cells, hVps34, has been studied extensively in the context of endocytic sorting. However, hVps34 also plays an important role in the ability of cells to respond to changes in nutrient conditions. Recent studies have shown that mammalian hVps34 is required for the activation of the mTOR (mammalian target of rapamycin)/S6K1 (S6 kinase 1) pathway, which regulates protein synthesis in response to nutrient availability. In both yeast and mammalian cells, Class III PI3Ks are also required for the induction of autophagy during nutrient deprivation. Finally, mammalian hVps34 is itself regulated by nutrients. Thus Class III PI3Ks are implicated in the regulation of both autophagy and, through the mTOR pathway, protein synthesis, and thus contribute to the integration of cellular responses to changing nutritional status.


2007 ◽  
Vol 74 (1) ◽  
pp. 47 ◽  
Author(s):  
Hsiangling Teo ◽  
David J. Gill ◽  
Ji Sun ◽  
Olga Perisic ◽  
Dmitry B. Veprintsev ◽  
...  

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