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Inductive asymmetric cell division: The WRM leads the way

C. elegans, with its invariant cell lineage, provides a powerful model system in which to study signaling-dependent asymmetric cell division. The C. elegans β-catenin-related protein, WRM-1, specifies endoderm at the 4-cell stage during the first cell signaling-induced asymmetric cell division of em...

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Autores principales: Ishidate, Takao, Kim, Soyoung, Mello, Craig C, Shirayama, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913193/
https://www.ncbi.nlm.nih.gov/pubmed/24524013
http://dx.doi.org/10.4161/worm.26276
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author Ishidate, Takao
Kim, Soyoung
Mello, Craig C
Shirayama, Masaki
author_facet Ishidate, Takao
Kim, Soyoung
Mello, Craig C
Shirayama, Masaki
author_sort Ishidate, Takao
collection PubMed
description C. elegans, with its invariant cell lineage, provides a powerful model system in which to study signaling-dependent asymmetric cell division. The C. elegans β-catenin-related protein, WRM-1, specifies endoderm at the 4-cell stage during the first cell signaling-induced asymmetric cell division of embryogenesis. During this interaction, Wnt signaling and the cell cycle regulator CDK-1 act together to induce the asymmetric cortical release of WRM-1 at prophase of the EMS cell cycle. Genetic studies suggest that release of WRM-1 unmasks a cortical site that drives EMS spindle rotation onto the polarized axis of the cell, simultaneously making WRM-1 available for nuclear translocation, and downstream signaling to specify endoderm. These studies suggest a general paradigm for how cortical factors like WRM-1 can function at the cell cortex to mask potentially confounding polarity cues, and when released with appropriate cell cycle timing, can also function downstream to define cell fate.
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spelling pubmed-39131932014-02-12 Inductive asymmetric cell division: The WRM leads the way Ishidate, Takao Kim, Soyoung Mello, Craig C Shirayama, Masaki Worm Mini Review C. elegans, with its invariant cell lineage, provides a powerful model system in which to study signaling-dependent asymmetric cell division. The C. elegans β-catenin-related protein, WRM-1, specifies endoderm at the 4-cell stage during the first cell signaling-induced asymmetric cell division of embryogenesis. During this interaction, Wnt signaling and the cell cycle regulator CDK-1 act together to induce the asymmetric cortical release of WRM-1 at prophase of the EMS cell cycle. Genetic studies suggest that release of WRM-1 unmasks a cortical site that drives EMS spindle rotation onto the polarized axis of the cell, simultaneously making WRM-1 available for nuclear translocation, and downstream signaling to specify endoderm. These studies suggest a general paradigm for how cortical factors like WRM-1 can function at the cell cortex to mask potentially confounding polarity cues, and when released with appropriate cell cycle timing, can also function downstream to define cell fate. Landes Bioscience 2013-10-01 2013-09-05 /pmc/articles/PMC3913193/ /pubmed/24524013 http://dx.doi.org/10.4161/worm.26276 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Mini Review
Ishidate, Takao
Kim, Soyoung
Mello, Craig C
Shirayama, Masaki
Inductive asymmetric cell division: The WRM leads the way
title Inductive asymmetric cell division: The WRM leads the way
title_full Inductive asymmetric cell division: The WRM leads the way
title_fullStr Inductive asymmetric cell division: The WRM leads the way
title_full_unstemmed Inductive asymmetric cell division: The WRM leads the way
title_short Inductive asymmetric cell division: The WRM leads the way
title_sort inductive asymmetric cell division: the wrm leads the way
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913193/
https://www.ncbi.nlm.nih.gov/pubmed/24524013
http://dx.doi.org/10.4161/worm.26276
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