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The period of the somite segmentation clock is sensitive to Notch activity

The number of vertebrae is defined strictly for a given species and depends on the number of somites, which are the earliest metameric structures that form in development. Somites are formed by sequential segmentation. The periodicity of somite segmentation is orchestrated by the synchronous oscilla...

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Autores principales: Kim, Woong, Matsui, Takaaki, Yamao, Masataka, Ishibashi, Makoto, Tamada, Kota, Takumi, Toru, Kohno, Kenji, Oba, Shigeyuki, Ishii, Shin, Sakumura, Yuichi, Bessho, Yasumasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172277/
https://www.ncbi.nlm.nih.gov/pubmed/21795391
http://dx.doi.org/10.1091/mbc.E11-02-0139
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author Kim, Woong
Matsui, Takaaki
Yamao, Masataka
Ishibashi, Makoto
Tamada, Kota
Takumi, Toru
Kohno, Kenji
Oba, Shigeyuki
Ishii, Shin
Sakumura, Yuichi
Bessho, Yasumasa
author_facet Kim, Woong
Matsui, Takaaki
Yamao, Masataka
Ishibashi, Makoto
Tamada, Kota
Takumi, Toru
Kohno, Kenji
Oba, Shigeyuki
Ishii, Shin
Sakumura, Yuichi
Bessho, Yasumasa
author_sort Kim, Woong
collection PubMed
description The number of vertebrae is defined strictly for a given species and depends on the number of somites, which are the earliest metameric structures that form in development. Somites are formed by sequential segmentation. The periodicity of somite segmentation is orchestrated by the synchronous oscillation of gene expression in the presomitic mesoderm (PSM), termed the “somite segmentation clock,” in which Notch signaling plays a crucial role. Here we show that the clock period is sensitive to Notch activity, which is fine-tuned by its feedback regulator, Notch-regulated ankyrin repeat protein (Nrarp), and that Nrarp is essential for forming the proper number and morphology of axial skeleton components. Null-mutant mice for Nrarp have fewer vertebrae and have defective morphologies. Notch activity is enhanced in the PSM of the Nrarp(−/–) embryo, where the ∼2-h segmentation period is extended by 5 min, thereby forming fewer somites and their resultant vertebrae. Reduced Notch activity partially rescues the Nrarp(−/–) phenotype in the number of somites, but not in morphology. Therefore we propose that the period of the somite segmentation clock is sensitive to Notch activity and that Nrarp plays essential roles in the morphology of vertebrae and ribs.
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spelling pubmed-31722772011-11-30 The period of the somite segmentation clock is sensitive to Notch activity Kim, Woong Matsui, Takaaki Yamao, Masataka Ishibashi, Makoto Tamada, Kota Takumi, Toru Kohno, Kenji Oba, Shigeyuki Ishii, Shin Sakumura, Yuichi Bessho, Yasumasa Mol Biol Cell Articles The number of vertebrae is defined strictly for a given species and depends on the number of somites, which are the earliest metameric structures that form in development. Somites are formed by sequential segmentation. The periodicity of somite segmentation is orchestrated by the synchronous oscillation of gene expression in the presomitic mesoderm (PSM), termed the “somite segmentation clock,” in which Notch signaling plays a crucial role. Here we show that the clock period is sensitive to Notch activity, which is fine-tuned by its feedback regulator, Notch-regulated ankyrin repeat protein (Nrarp), and that Nrarp is essential for forming the proper number and morphology of axial skeleton components. Null-mutant mice for Nrarp have fewer vertebrae and have defective morphologies. Notch activity is enhanced in the PSM of the Nrarp(−/–) embryo, where the ∼2-h segmentation period is extended by 5 min, thereby forming fewer somites and their resultant vertebrae. Reduced Notch activity partially rescues the Nrarp(−/–) phenotype in the number of somites, but not in morphology. Therefore we propose that the period of the somite segmentation clock is sensitive to Notch activity and that Nrarp plays essential roles in the morphology of vertebrae and ribs. The American Society for Cell Biology 2011-09-15 /pmc/articles/PMC3172277/ /pubmed/21795391 http://dx.doi.org/10.1091/mbc.E11-02-0139 Text en © 2011 Kim et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Kim, Woong
Matsui, Takaaki
Yamao, Masataka
Ishibashi, Makoto
Tamada, Kota
Takumi, Toru
Kohno, Kenji
Oba, Shigeyuki
Ishii, Shin
Sakumura, Yuichi
Bessho, Yasumasa
The period of the somite segmentation clock is sensitive to Notch activity
title The period of the somite segmentation clock is sensitive to Notch activity
title_full The period of the somite segmentation clock is sensitive to Notch activity
title_fullStr The period of the somite segmentation clock is sensitive to Notch activity
title_full_unstemmed The period of the somite segmentation clock is sensitive to Notch activity
title_short The period of the somite segmentation clock is sensitive to Notch activity
title_sort period of the somite segmentation clock is sensitive to notch activity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172277/
https://www.ncbi.nlm.nih.gov/pubmed/21795391
http://dx.doi.org/10.1091/mbc.E11-02-0139
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