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Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements
Regulation of cytoskeletal remodeling is essential for cell cycle transitions. In fission yeast two NDR kinase signaling cascades, MOR and SIN, regulate the actin cytoskeleton to promote polarized growth during interphase and cytokinesis respectively. Our understanding of how these signaling pathway...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224761/ https://www.ncbi.nlm.nih.gov/pubmed/22079013 http://dx.doi.org/10.1186/1747-1028-6-19 |
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author | Gupta, Sneha McCollum, Dannel |
author_facet | Gupta, Sneha McCollum, Dannel |
author_sort | Gupta, Sneha |
collection | PubMed |
description | Regulation of cytoskeletal remodeling is essential for cell cycle transitions. In fission yeast two NDR kinase signaling cascades, MOR and SIN, regulate the actin cytoskeleton to promote polarized growth during interphase and cytokinesis respectively. Our understanding of how these signaling pathways are coordinated to assist transition between the two cell-cycle stages is limited. Here, we review work from our laboratory, which reveals that cross talk between the SIN and MOR pathways is required for inhibition of interphase polarity programs during cytokinesis. Given the conservation of NDR kinase signaling pathways, our results may define general mechanisms by which these pathways are coordinated in higher organisms. |
format | Online Article Text |
id | pubmed-3224761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32247612011-11-28 Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements Gupta, Sneha McCollum, Dannel Cell Div Commentary Regulation of cytoskeletal remodeling is essential for cell cycle transitions. In fission yeast two NDR kinase signaling cascades, MOR and SIN, regulate the actin cytoskeleton to promote polarized growth during interphase and cytokinesis respectively. Our understanding of how these signaling pathways are coordinated to assist transition between the two cell-cycle stages is limited. Here, we review work from our laboratory, which reveals that cross talk between the SIN and MOR pathways is required for inhibition of interphase polarity programs during cytokinesis. Given the conservation of NDR kinase signaling pathways, our results may define general mechanisms by which these pathways are coordinated in higher organisms. BioMed Central 2011-11-11 /pmc/articles/PMC3224761/ /pubmed/22079013 http://dx.doi.org/10.1186/1747-1028-6-19 Text en Copyright ©2011 Gupta and McCollum; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Gupta, Sneha McCollum, Dannel Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title | Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title_full | Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title_fullStr | Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title_full_unstemmed | Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title_short | Crosstalk between NDR kinase pathways coordinates cell cycle dependent actin rearrangements |
title_sort | crosstalk between ndr kinase pathways coordinates cell cycle dependent actin rearrangements |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224761/ https://www.ncbi.nlm.nih.gov/pubmed/22079013 http://dx.doi.org/10.1186/1747-1028-6-19 |
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