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The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling
Inactivation of the tumor suppressor NF2/merlin underlies neurofibromatosis type 2 (NF2) and some sporadic tumors. Previous studies have established that merlin mediates contact inhibition of proliferation; however, the exact mechanisms remain obscure and multiple pathways have been implicated. We h...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756068/ https://www.ncbi.nlm.nih.gov/pubmed/31312020 http://dx.doi.org/10.1038/s41388-019-0883-6 |
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author | Cui, Yan Groth, Susann Troutman, Scott Carlstedt, Annemarie Sperka, Tobias Riecken, Lars Björn Kissil, Joseph L. Jin, Hongchuan Morrison, Helen |
author_facet | Cui, Yan Groth, Susann Troutman, Scott Carlstedt, Annemarie Sperka, Tobias Riecken, Lars Björn Kissil, Joseph L. Jin, Hongchuan Morrison, Helen |
author_sort | Cui, Yan |
collection | PubMed |
description | Inactivation of the tumor suppressor NF2/merlin underlies neurofibromatosis type 2 (NF2) and some sporadic tumors. Previous studies have established that merlin mediates contact inhibition of proliferation; however, the exact mechanisms remain obscure and multiple pathways have been implicated. We have previously reported that merlin inhibits Ras and Rac activity during contact inhibition, but how merlin regulates Ras activity has remained elusive. Here we demonstrate that merlin can directly interact with both Ras and p120RasGAP (also named RasGAP). While merlin does not increase the catalytic activity of RasGAP, the interactions with Ras and RasGAP may fine-tune Ras signaling. In vivo, loss of RasGAP in Schwann cells, unlike the loss of merlin, failed to promote tumorigenic growth in an orthotopic model. Therefore, modulation of Ras signaling through RasGAP likely contributes to, but is not sufficient to account for, merlin’s tumor suppressor activity. Our study provides new insight into the mechanisms of merlin-dependent Ras regulation and may have additional implications for merlin-dependent regulation of other small GTPases. |
format | Online Article Text |
id | pubmed-6756068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67560682019-09-24 The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling Cui, Yan Groth, Susann Troutman, Scott Carlstedt, Annemarie Sperka, Tobias Riecken, Lars Björn Kissil, Joseph L. Jin, Hongchuan Morrison, Helen Oncogene Article Inactivation of the tumor suppressor NF2/merlin underlies neurofibromatosis type 2 (NF2) and some sporadic tumors. Previous studies have established that merlin mediates contact inhibition of proliferation; however, the exact mechanisms remain obscure and multiple pathways have been implicated. We have previously reported that merlin inhibits Ras and Rac activity during contact inhibition, but how merlin regulates Ras activity has remained elusive. Here we demonstrate that merlin can directly interact with both Ras and p120RasGAP (also named RasGAP). While merlin does not increase the catalytic activity of RasGAP, the interactions with Ras and RasGAP may fine-tune Ras signaling. In vivo, loss of RasGAP in Schwann cells, unlike the loss of merlin, failed to promote tumorigenic growth in an orthotopic model. Therefore, modulation of Ras signaling through RasGAP likely contributes to, but is not sufficient to account for, merlin’s tumor suppressor activity. Our study provides new insight into the mechanisms of merlin-dependent Ras regulation and may have additional implications for merlin-dependent regulation of other small GTPases. Nature Publishing Group UK 2019-07-16 2019 /pmc/articles/PMC6756068/ /pubmed/31312020 http://dx.doi.org/10.1038/s41388-019-0883-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cui, Yan Groth, Susann Troutman, Scott Carlstedt, Annemarie Sperka, Tobias Riecken, Lars Björn Kissil, Joseph L. Jin, Hongchuan Morrison, Helen The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title | The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title_full | The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title_fullStr | The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title_full_unstemmed | The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title_short | The NF2 tumor suppressor merlin interacts with Ras and RasGAP, which may modulate Ras signaling |
title_sort | nf2 tumor suppressor merlin interacts with ras and rasgap, which may modulate ras signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756068/ https://www.ncbi.nlm.nih.gov/pubmed/31312020 http://dx.doi.org/10.1038/s41388-019-0883-6 |
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