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The function of Shoc2: A scaffold and beyond
The extracellular signal-regulated kinase (ERK1/2) cascade regulates a myriad of functions in multicellular organisms. Scaffold proteins provide critical spatial and temporal control over the specificity of signaling. Shoc2 is a scaffold that accelerates activity of the ERK1/2 pathway. Loss of Shoc2...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988449/ https://www.ncbi.nlm.nih.gov/pubmed/27574535 http://dx.doi.org/10.1080/19420889.2016.1188241 |
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author | Jang, Eun Ryoung Galperin, Emilia |
author_facet | Jang, Eun Ryoung Galperin, Emilia |
author_sort | Jang, Eun Ryoung |
collection | PubMed |
description | The extracellular signal-regulated kinase (ERK1/2) cascade regulates a myriad of functions in multicellular organisms. Scaffold proteins provide critical spatial and temporal control over the specificity of signaling. Shoc2 is a scaffold that accelerates activity of the ERK1/2 pathway. Loss of Shoc2 expression in mice results in embryonic lethality, thus highlighting the essential role of Shoc2 in embryogenesis. In agreement, patients carrying mutated Shoc2 suffer from a wide spectrum of developmental deficiencies. Efforts to understand the mechanisms by which Shoc2 controls ERK1/2 activity revealed the intricate machinery that governs the ability of Shoc2 to transduce signals of the ERK1/2 pathway. Understanding the mechanisms by which Shoc2 contributes to a high degree of specificity of ERK1/2 signaling as well as deciphering the biological functions of Shoc2 in development and human disorders are major unresolved questions. |
format | Online Article Text |
id | pubmed-4988449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49884492016-08-29 The function of Shoc2: A scaffold and beyond Jang, Eun Ryoung Galperin, Emilia Commun Integr Biol Short Communication The extracellular signal-regulated kinase (ERK1/2) cascade regulates a myriad of functions in multicellular organisms. Scaffold proteins provide critical spatial and temporal control over the specificity of signaling. Shoc2 is a scaffold that accelerates activity of the ERK1/2 pathway. Loss of Shoc2 expression in mice results in embryonic lethality, thus highlighting the essential role of Shoc2 in embryogenesis. In agreement, patients carrying mutated Shoc2 suffer from a wide spectrum of developmental deficiencies. Efforts to understand the mechanisms by which Shoc2 controls ERK1/2 activity revealed the intricate machinery that governs the ability of Shoc2 to transduce signals of the ERK1/2 pathway. Understanding the mechanisms by which Shoc2 contributes to a high degree of specificity of ERK1/2 signaling as well as deciphering the biological functions of Shoc2 in development and human disorders are major unresolved questions. Taylor & Francis 2016-05-18 /pmc/articles/PMC4988449/ /pubmed/27574535 http://dx.doi.org/10.1080/19420889.2016.1188241 Text en © 2016 The Author(s). Published with license by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Short Communication Jang, Eun Ryoung Galperin, Emilia The function of Shoc2: A scaffold and beyond |
title | The function of Shoc2: A scaffold and beyond |
title_full | The function of Shoc2: A scaffold and beyond |
title_fullStr | The function of Shoc2: A scaffold and beyond |
title_full_unstemmed | The function of Shoc2: A scaffold and beyond |
title_short | The function of Shoc2: A scaffold and beyond |
title_sort | function of shoc2: a scaffold and beyond |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988449/ https://www.ncbi.nlm.nih.gov/pubmed/27574535 http://dx.doi.org/10.1080/19420889.2016.1188241 |
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