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Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity
Cytokinesis, the physical division of one cell into two, is powered by constriction of an actomyosin contractile ring. It has long been assumed that all animal cells divide by a similar molecular mechanism, but growing evidence suggests that cytokinetic regulation in individual cell types has more v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054530/ https://www.ncbi.nlm.nih.gov/pubmed/30028292 http://dx.doi.org/10.7554/eLife.36204 |
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author | Davies, Tim Kim, Han X Romano Spica, Natalia Lesea-Pringle, Benjamin J Dumont, Julien Shirasu-Hiza, Mimi Canman, Julie C |
author_facet | Davies, Tim Kim, Han X Romano Spica, Natalia Lesea-Pringle, Benjamin J Dumont, Julien Shirasu-Hiza, Mimi Canman, Julie C |
author_sort | Davies, Tim |
collection | PubMed |
description | Cytokinesis, the physical division of one cell into two, is powered by constriction of an actomyosin contractile ring. It has long been assumed that all animal cells divide by a similar molecular mechanism, but growing evidence suggests that cytokinetic regulation in individual cell types has more variation than previously realized. In the four-cell Caenorhabditis elegans embryo, each blastomere has a distinct cell fate, specified by conserved pathways. Using fast-acting temperature-sensitive mutants and acute drug treatment, we identified cell-type-specific variation in the cytokinetic requirement for a robust formin(CYK-1)-dependent filamentous-actin (F-actin) cytoskeleton. In one cell (P2), this cytokinetic variation is cell-intrinsically regulated, whereas in another cell (EMS) this variation is cell-extrinsically regulated, dependent on both Src(SRC-1) signaling and direct contact with its neighbor cell, P2. Thus, both cell-intrinsic and -extrinsic mechanisms control cytokinetic variation in individual cell types and can protect against division failure when the contractile ring is weakened. |
format | Online Article Text |
id | pubmed-6054530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60545302018-07-23 Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity Davies, Tim Kim, Han X Romano Spica, Natalia Lesea-Pringle, Benjamin J Dumont, Julien Shirasu-Hiza, Mimi Canman, Julie C eLife Cell Biology Cytokinesis, the physical division of one cell into two, is powered by constriction of an actomyosin contractile ring. It has long been assumed that all animal cells divide by a similar molecular mechanism, but growing evidence suggests that cytokinetic regulation in individual cell types has more variation than previously realized. In the four-cell Caenorhabditis elegans embryo, each blastomere has a distinct cell fate, specified by conserved pathways. Using fast-acting temperature-sensitive mutants and acute drug treatment, we identified cell-type-specific variation in the cytokinetic requirement for a robust formin(CYK-1)-dependent filamentous-actin (F-actin) cytoskeleton. In one cell (P2), this cytokinetic variation is cell-intrinsically regulated, whereas in another cell (EMS) this variation is cell-extrinsically regulated, dependent on both Src(SRC-1) signaling and direct contact with its neighbor cell, P2. Thus, both cell-intrinsic and -extrinsic mechanisms control cytokinetic variation in individual cell types and can protect against division failure when the contractile ring is weakened. eLife Sciences Publications, Ltd 2018-07-20 /pmc/articles/PMC6054530/ /pubmed/30028292 http://dx.doi.org/10.7554/eLife.36204 Text en © 2018, Davies et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Davies, Tim Kim, Han X Romano Spica, Natalia Lesea-Pringle, Benjamin J Dumont, Julien Shirasu-Hiza, Mimi Canman, Julie C Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title_full | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title_fullStr | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title_full_unstemmed | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title_short | Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
title_sort | cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054530/ https://www.ncbi.nlm.nih.gov/pubmed/30028292 http://dx.doi.org/10.7554/eLife.36204 |
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