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Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo
The docking protein Gab1 binds phosphorylated c-Met receptor tyrosine kinase directly and mediates signals of c-Met in cell culture. Gab1 is phosphorylated by c-Met and by other receptor and nonreceptor tyrosine kinases. Here, we report the functional analysis of Gab1 by targeted mutagenesis in the...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150711/ https://www.ncbi.nlm.nih.gov/pubmed/10995442 |
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author | Sachs, Martin Brohmann, Henning Zechner, Dietmar Müller, Thomas Hülsken, Jörg Walther, Ingrid Schaeper, Ute Birchmeier, Carmen Birchmeier, Walter |
author_facet | Sachs, Martin Brohmann, Henning Zechner, Dietmar Müller, Thomas Hülsken, Jörg Walther, Ingrid Schaeper, Ute Birchmeier, Carmen Birchmeier, Walter |
author_sort | Sachs, Martin |
collection | PubMed |
description | The docking protein Gab1 binds phosphorylated c-Met receptor tyrosine kinase directly and mediates signals of c-Met in cell culture. Gab1 is phosphorylated by c-Met and by other receptor and nonreceptor tyrosine kinases. Here, we report the functional analysis of Gab1 by targeted mutagenesis in the mouse, and compare the phenotypes of the Gab1 and c-Met mutations. Gab1 is essential for several steps in development: migration of myogenic precursor cells into the limb anlage is impaired in Gab1−/− embryos. As a consequence, extensor muscle groups of the forelimbs are virtually absent, and the flexor muscles reach less far. Fewer hindlimb muscles exist, which are smaller and disorganized. Muscles in the diaphragm, which also originate from migratory precursors, are missing. Moreover, Gab1−/− embryos die in a broad time window between E13.5 and E18.5, and display reduced liver size and placental defects. The labyrinth layer, but not the spongiotrophoblast layer, of the placenta is severely reduced, resulting in impaired communication between maternal and fetal circulation. Thus, extensive similarities between the phenotypes of c-Met and HGF/SF mutant mice exist, and the muscle migration phenotype is even more pronounced in Gab1−/−:c-Met+/− embryos. This is genetic evidence that Gab1 is essential for c-Met signaling in vivo. Analogy exists to signal transmission by insulin receptors, which require IRS1 and IRS2 as specific docking proteins. |
format | Text |
id | pubmed-2150711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21507112008-05-01 Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo Sachs, Martin Brohmann, Henning Zechner, Dietmar Müller, Thomas Hülsken, Jörg Walther, Ingrid Schaeper, Ute Birchmeier, Carmen Birchmeier, Walter J Cell Biol Original Article The docking protein Gab1 binds phosphorylated c-Met receptor tyrosine kinase directly and mediates signals of c-Met in cell culture. Gab1 is phosphorylated by c-Met and by other receptor and nonreceptor tyrosine kinases. Here, we report the functional analysis of Gab1 by targeted mutagenesis in the mouse, and compare the phenotypes of the Gab1 and c-Met mutations. Gab1 is essential for several steps in development: migration of myogenic precursor cells into the limb anlage is impaired in Gab1−/− embryos. As a consequence, extensor muscle groups of the forelimbs are virtually absent, and the flexor muscles reach less far. Fewer hindlimb muscles exist, which are smaller and disorganized. Muscles in the diaphragm, which also originate from migratory precursors, are missing. Moreover, Gab1−/− embryos die in a broad time window between E13.5 and E18.5, and display reduced liver size and placental defects. The labyrinth layer, but not the spongiotrophoblast layer, of the placenta is severely reduced, resulting in impaired communication between maternal and fetal circulation. Thus, extensive similarities between the phenotypes of c-Met and HGF/SF mutant mice exist, and the muscle migration phenotype is even more pronounced in Gab1−/−:c-Met+/− embryos. This is genetic evidence that Gab1 is essential for c-Met signaling in vivo. Analogy exists to signal transmission by insulin receptors, which require IRS1 and IRS2 as specific docking proteins. The Rockefeller University Press 2000-09-18 /pmc/articles/PMC2150711/ /pubmed/10995442 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Sachs, Martin Brohmann, Henning Zechner, Dietmar Müller, Thomas Hülsken, Jörg Walther, Ingrid Schaeper, Ute Birchmeier, Carmen Birchmeier, Walter Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title | Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title_full | Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title_fullStr | Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title_full_unstemmed | Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title_short | Essential Role of Gab1 for Signaling by the C-Met Receptor in Vivo |
title_sort | essential role of gab1 for signaling by the c-met receptor in vivo |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150711/ https://www.ncbi.nlm.nih.gov/pubmed/10995442 |
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