In vivo analysis of the Notch receptor S1 cleavage.
A ligand-independent cleavage (S1) in the extracellular domain of the mammalian Notch receptor results in what is considered to be the canonical heterodimeric form of Notch on the cell surface. The in vivo consequences and significance of this cleavage on Drosophila Notch signaling remain unclear an...
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Public Library of Science (PLoS)
2009
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oai:doaj.org-article:05d2fdc75ee043be924eac48fa9137ac2021-11-25T06:20:52ZIn vivo analysis of the Notch receptor S1 cleavage.1932-620310.1371/journal.pone.0006728https://doaj.org/article/05d2fdc75ee043be924eac48fa9137ac2009-08-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19701455/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203A ligand-independent cleavage (S1) in the extracellular domain of the mammalian Notch receptor results in what is considered to be the canonical heterodimeric form of Notch on the cell surface. The in vivo consequences and significance of this cleavage on Drosophila Notch signaling remain unclear and contradictory. We determined the cleavage site in Drosophila and examined its in vivo function by a transgenic analysis of receptors that cannot be cleaved. Our results demonstrate a correlation between loss of cleavage and loss of in vivo function of the Notch receptor, supporting the notion that S1 cleavage is an in vivo mechanism of Notch signal control.Robert J LakeLisa M GrimmAlexey VeraksaAndrew BanosSpyros Artavanis-TsakonasPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 4, Iss 8, p e6728 (2009) |
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Medicine R Science Q Robert J Lake Lisa M Grimm Alexey Veraksa Andrew Banos Spyros Artavanis-Tsakonas In vivo analysis of the Notch receptor S1 cleavage. |
description |
A ligand-independent cleavage (S1) in the extracellular domain of the mammalian Notch receptor results in what is considered to be the canonical heterodimeric form of Notch on the cell surface. The in vivo consequences and significance of this cleavage on Drosophila Notch signaling remain unclear and contradictory. We determined the cleavage site in Drosophila and examined its in vivo function by a transgenic analysis of receptors that cannot be cleaved. Our results demonstrate a correlation between loss of cleavage and loss of in vivo function of the Notch receptor, supporting the notion that S1 cleavage is an in vivo mechanism of Notch signal control. |
format |
article |
author |
Robert J Lake Lisa M Grimm Alexey Veraksa Andrew Banos Spyros Artavanis-Tsakonas |
author_facet |
Robert J Lake Lisa M Grimm Alexey Veraksa Andrew Banos Spyros Artavanis-Tsakonas |
author_sort |
Robert J Lake |
title |
In vivo analysis of the Notch receptor S1 cleavage. |
title_short |
In vivo analysis of the Notch receptor S1 cleavage. |
title_full |
In vivo analysis of the Notch receptor S1 cleavage. |
title_fullStr |
In vivo analysis of the Notch receptor S1 cleavage. |
title_full_unstemmed |
In vivo analysis of the Notch receptor S1 cleavage. |
title_sort |
in vivo analysis of the notch receptor s1 cleavage. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2009 |
url |
https://doaj.org/article/05d2fdc75ee043be924eac48fa9137ac |
work_keys_str_mv |
AT robertjlake invivoanalysisofthenotchreceptors1cleavage AT lisamgrimm invivoanalysisofthenotchreceptors1cleavage AT alexeyveraksa invivoanalysisofthenotchreceptors1cleavage AT andrewbanos invivoanalysisofthenotchreceptors1cleavage AT spyrosartavanistsakonas invivoanalysisofthenotchreceptors1cleavage |
_version_ |
1718413783946231808 |