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Regulation of synaptojanin 2 5′-phosphatase activity by Src

Synaptojanin 2 (SYNJ2) is a phosphatidylinositol (PI) phosphatase that controls two distinct functions, clathrin-mediated endocytosis and tumor cell invadopodia formation and invasion. Here, we identify a number of novel SYNJ2 binding partners, several of which have previously been shown to be neces...

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Autores principales: Chuang, Yayu, Xu, Xiaonan, Kwiatkowska, Aneta, Tsapraillis, George, Hwang, Hyonson, Petritis, Konstantinos, Flynn, Dan, Symons, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547897/
https://www.ncbi.nlm.nih.gov/pubmed/23076136
http://dx.doi.org/10.4161/cam.22139
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author Chuang, Yayu
Xu, Xiaonan
Kwiatkowska, Aneta
Tsapraillis, George
Hwang, Hyonson
Petritis, Konstantinos
Flynn, Dan
Symons, Marc
author_facet Chuang, Yayu
Xu, Xiaonan
Kwiatkowska, Aneta
Tsapraillis, George
Hwang, Hyonson
Petritis, Konstantinos
Flynn, Dan
Symons, Marc
author_sort Chuang, Yayu
collection PubMed
description Synaptojanin 2 (SYNJ2) is a phosphatidylinositol (PI) phosphatase that controls two distinct functions, clathrin-mediated endocytosis and tumor cell invadopodia formation and invasion. Here, we identify a number of novel SYNJ2 binding partners, several of which have previously been shown to be necessary for invadopodia formation or clathrin-mediated endocytosis. We focus on Src family kinases. We found that Src phosphorylates SYNJ2 on Tyr(490), thereby stimulating SYNJ2 5′-phosphatase activity in vitro. We also provide evidence that Src-mediated phosphorylation of SYNJ2 contributes to invadopodia formation.
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spelling pubmed-35478972013-01-30 Regulation of synaptojanin 2 5′-phosphatase activity by Src Chuang, Yayu Xu, Xiaonan Kwiatkowska, Aneta Tsapraillis, George Hwang, Hyonson Petritis, Konstantinos Flynn, Dan Symons, Marc Cell Adh Migr Research Paper Synaptojanin 2 (SYNJ2) is a phosphatidylinositol (PI) phosphatase that controls two distinct functions, clathrin-mediated endocytosis and tumor cell invadopodia formation and invasion. Here, we identify a number of novel SYNJ2 binding partners, several of which have previously been shown to be necessary for invadopodia formation or clathrin-mediated endocytosis. We focus on Src family kinases. We found that Src phosphorylates SYNJ2 on Tyr(490), thereby stimulating SYNJ2 5′-phosphatase activity in vitro. We also provide evidence that Src-mediated phosphorylation of SYNJ2 contributes to invadopodia formation. Landes Bioscience 2012-11-01 /pmc/articles/PMC3547897/ /pubmed/23076136 http://dx.doi.org/10.4161/cam.22139 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Chuang, Yayu
Xu, Xiaonan
Kwiatkowska, Aneta
Tsapraillis, George
Hwang, Hyonson
Petritis, Konstantinos
Flynn, Dan
Symons, Marc
Regulation of synaptojanin 2 5′-phosphatase activity by Src
title Regulation of synaptojanin 2 5′-phosphatase activity by Src
title_full Regulation of synaptojanin 2 5′-phosphatase activity by Src
title_fullStr Regulation of synaptojanin 2 5′-phosphatase activity by Src
title_full_unstemmed Regulation of synaptojanin 2 5′-phosphatase activity by Src
title_short Regulation of synaptojanin 2 5′-phosphatase activity by Src
title_sort regulation of synaptojanin 2 5′-phosphatase activity by src
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547897/
https://www.ncbi.nlm.nih.gov/pubmed/23076136
http://dx.doi.org/10.4161/cam.22139
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