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Making parallel lines meet: Transferring information from microtubules to extracellular matrix
The extracellular matrix is constructed beyond the plasma membrane, challenging mechanisms for its control by the cell. In plants, the cell wall is highly ordered, with cellulose microfibrils aligned coherently over a scale spanning hundreds of cells. To a considerable extent, deploying aligned micr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496676/ https://www.ncbi.nlm.nih.gov/pubmed/22902763 http://dx.doi.org/10.4161/cam.21121 |
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author | Baskin, Tobias I. Gu, Ying |
author_facet | Baskin, Tobias I. Gu, Ying |
author_sort | Baskin, Tobias I. |
collection | PubMed |
description | The extracellular matrix is constructed beyond the plasma membrane, challenging mechanisms for its control by the cell. In plants, the cell wall is highly ordered, with cellulose microfibrils aligned coherently over a scale spanning hundreds of cells. To a considerable extent, deploying aligned microfibrils determines mechanical properties of the cell wall, including strength and compliance. Cellulose microfibrils have long been seen to be aligned in parallel with an array of microtubules in the cell cortex. How do these cortical microtubules affect the cellulose synthase complex? This question has stood for as many years as the parallelism between the elements has been observed, but now an answer is emerging. Here, we review recent work establishing that the link between microtubules and microfibrils is mediated by a protein named cellulose synthase-interacting protein 1 (CSI1). The protein binds both microtubules and components of the cellulose synthase complex. In the absence of CSI1, microfibrils are synthesized but their alignment becomes uncoupled from the microtubules, an effect that is phenocopied in the wild type by depolymerizing the microtubules. The characterization of CSI1 significantly enhances knowledge of how cellulose is aligned, a process that serves as a paradigmatic example of how cells dictate the construction of their extracellular environment. |
format | Online Article Text |
id | pubmed-3496676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-34966762012-11-23 Making parallel lines meet: Transferring information from microtubules to extracellular matrix Baskin, Tobias I. Gu, Ying Cell Adh Migr Commentary The extracellular matrix is constructed beyond the plasma membrane, challenging mechanisms for its control by the cell. In plants, the cell wall is highly ordered, with cellulose microfibrils aligned coherently over a scale spanning hundreds of cells. To a considerable extent, deploying aligned microfibrils determines mechanical properties of the cell wall, including strength and compliance. Cellulose microfibrils have long been seen to be aligned in parallel with an array of microtubules in the cell cortex. How do these cortical microtubules affect the cellulose synthase complex? This question has stood for as many years as the parallelism between the elements has been observed, but now an answer is emerging. Here, we review recent work establishing that the link between microtubules and microfibrils is mediated by a protein named cellulose synthase-interacting protein 1 (CSI1). The protein binds both microtubules and components of the cellulose synthase complex. In the absence of CSI1, microfibrils are synthesized but their alignment becomes uncoupled from the microtubules, an effect that is phenocopied in the wild type by depolymerizing the microtubules. The characterization of CSI1 significantly enhances knowledge of how cellulose is aligned, a process that serves as a paradigmatic example of how cells dictate the construction of their extracellular environment. Landes Bioscience 2012-09-01 /pmc/articles/PMC3496676/ /pubmed/22902763 http://dx.doi.org/10.4161/cam.21121 Text en Copyright © 2012 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 | Commentary Baskin, Tobias I. Gu, Ying Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title | Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title_full | Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title_fullStr | Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title_full_unstemmed | Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title_short | Making parallel lines meet: Transferring information from microtubules to extracellular matrix |
title_sort | making parallel lines meet: transferring information from microtubules to extracellular matrix |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496676/ https://www.ncbi.nlm.nih.gov/pubmed/22902763 http://dx.doi.org/10.4161/cam.21121 |
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