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Dissecting the contribution of microtubule behaviour in adventitious root induction
Induction of adventitious roots (ARs) in recalcitrant plants often culminates in cell division and callus formation rather than root differentiation. Evidence is provided here to suggest that microtubules (MTs) play a role in the shift from cell division to cell differentiation during AR induction....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986881/ https://www.ncbi.nlm.nih.gov/pubmed/25788735 http://dx.doi.org/10.1093/jxb/erv097 |
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author | Abu-Abied, Mohamad Rogovoy (Stelmakh), Oksana Mordehaev, Inna Grumberg, Marina Elbaum, Rivka Wasteneys, Geoffrey O. Sadot, Einat |
author_facet | Abu-Abied, Mohamad Rogovoy (Stelmakh), Oksana Mordehaev, Inna Grumberg, Marina Elbaum, Rivka Wasteneys, Geoffrey O. Sadot, Einat |
author_sort | Abu-Abied, Mohamad |
collection | PubMed |
description | Induction of adventitious roots (ARs) in recalcitrant plants often culminates in cell division and callus formation rather than root differentiation. Evidence is provided here to suggest that microtubules (MTs) play a role in the shift from cell division to cell differentiation during AR induction. First, it was found that fewer ARs form in the temperature-sensitive mutant mor1-1, in which the MT-associated protein MOR1 is mutated, and in bot1-1, in which the MT-severing protein katanin is mutated. In the two latter mutants, MT dynamics and form are perturbed. By contrast, the number of ARs increased in RIC1-OX3 plants, in which MT bundling is enhanced and katanin is activated. In addition, any1 plants in which cell walls are perturbed made more ARs than wild-type plants. MT perturbations during AR induction in mor1-1 or in wild-type hypocotyls treated with oryzalin led to the formation of amorphous clusters of cells reminiscent of callus. In these cells a specific pattern of polarized light retardation by the cell walls was lost. PIN1 polarization and auxin maxima were hampered and differentiation of the epidermis was inhibited. It is concluded that a fine-tuned crosstalk between MTs, cell walls, and auxin transport is required for proper AR induction. |
format | Online Article Text |
id | pubmed-4986881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49868812016-08-22 Dissecting the contribution of microtubule behaviour in adventitious root induction Abu-Abied, Mohamad Rogovoy (Stelmakh), Oksana Mordehaev, Inna Grumberg, Marina Elbaum, Rivka Wasteneys, Geoffrey O. Sadot, Einat J Exp Bot Research Paper Induction of adventitious roots (ARs) in recalcitrant plants often culminates in cell division and callus formation rather than root differentiation. Evidence is provided here to suggest that microtubules (MTs) play a role in the shift from cell division to cell differentiation during AR induction. First, it was found that fewer ARs form in the temperature-sensitive mutant mor1-1, in which the MT-associated protein MOR1 is mutated, and in bot1-1, in which the MT-severing protein katanin is mutated. In the two latter mutants, MT dynamics and form are perturbed. By contrast, the number of ARs increased in RIC1-OX3 plants, in which MT bundling is enhanced and katanin is activated. In addition, any1 plants in which cell walls are perturbed made more ARs than wild-type plants. MT perturbations during AR induction in mor1-1 or in wild-type hypocotyls treated with oryzalin led to the formation of amorphous clusters of cells reminiscent of callus. In these cells a specific pattern of polarized light retardation by the cell walls was lost. PIN1 polarization and auxin maxima were hampered and differentiation of the epidermis was inhibited. It is concluded that a fine-tuned crosstalk between MTs, cell walls, and auxin transport is required for proper AR induction. Oxford University Press 2015-05 2015-03-18 /pmc/articles/PMC4986881/ /pubmed/25788735 http://dx.doi.org/10.1093/jxb/erv097 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Abu-Abied, Mohamad Rogovoy (Stelmakh), Oksana Mordehaev, Inna Grumberg, Marina Elbaum, Rivka Wasteneys, Geoffrey O. Sadot, Einat Dissecting the contribution of microtubule behaviour in adventitious root induction |
title | Dissecting the contribution of microtubule behaviour in adventitious root induction |
title_full | Dissecting the contribution of microtubule behaviour in adventitious root induction |
title_fullStr | Dissecting the contribution of microtubule behaviour in adventitious root induction |
title_full_unstemmed | Dissecting the contribution of microtubule behaviour in adventitious root induction |
title_short | Dissecting the contribution of microtubule behaviour in adventitious root induction |
title_sort | dissecting the contribution of microtubule behaviour in adventitious root induction |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986881/ https://www.ncbi.nlm.nih.gov/pubmed/25788735 http://dx.doi.org/10.1093/jxb/erv097 |
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