Cargando…

Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division

The interplay between myosin- and auxin-mediated processes was investigated by following root development in the triple myosin knockout mutant xi-k xi-1 xi-2 (3KO). It was found that the 3KO plants generated significantly more lateral and adventitious roots than the wild-type plants or the rescued p...

Descripción completa

Detalles Bibliográficos
Autores principales: Abu-Abied, Mohamad, Belausov, Eduard, Hagay, Sapir, Peremyslov, Valera, Dolja, Valerian, Sadot, Einat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972647/
https://www.ncbi.nlm.nih.gov/pubmed/29579267
http://dx.doi.org/10.1093/jxb/ery112
_version_ 1783326463346343936
author Abu-Abied, Mohamad
Belausov, Eduard
Hagay, Sapir
Peremyslov, Valera
Dolja, Valerian
Sadot, Einat
author_facet Abu-Abied, Mohamad
Belausov, Eduard
Hagay, Sapir
Peremyslov, Valera
Dolja, Valerian
Sadot, Einat
author_sort Abu-Abied, Mohamad
collection PubMed
description The interplay between myosin- and auxin-mediated processes was investigated by following root development in the triple myosin knockout mutant xi-k xi-1 xi-2 (3KO). It was found that the 3KO plants generated significantly more lateral and adventitious roots than the wild-type plants or the rescued plant line expressing functional myosin XI-K:yellow fluorescent protein (YFP; 3KOR). Using the auxin-dependent reporter DR5:venus, a significant change in the auxin gradient toward the root tip was found in 3KO plants, which correlated with the loss of polar localization of the auxin transporter PIN1 in the stele and with the increased number of stele cells with oblique cell walls. Interestingly, myosin XI-K:YFP was localized to the cell division apparatus in the root and shoot meristems. In anaphase and early telophase, XI-K:YFP was concentrated in the midzone and the forming cell plate. In late telophase, XI-K:YFP formed a ring that overlapped with the growing phragmoplast. Myosin receptors MyoB1 and MyoB2 that are highly expressed throughout the plant were undetectable in dividing cells, suggesting that the myosin function in cell division relies on distinct adaptor proteins. These results suggest that myosin XIs are involved in orchestrating root organogenesis via effects on polar distribution of auxin responses and on cell division.
format Online
Article
Text
id pubmed-5972647
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-59726472018-06-04 Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division Abu-Abied, Mohamad Belausov, Eduard Hagay, Sapir Peremyslov, Valera Dolja, Valerian Sadot, Einat J Exp Bot Research Papers The interplay between myosin- and auxin-mediated processes was investigated by following root development in the triple myosin knockout mutant xi-k xi-1 xi-2 (3KO). It was found that the 3KO plants generated significantly more lateral and adventitious roots than the wild-type plants or the rescued plant line expressing functional myosin XI-K:yellow fluorescent protein (YFP; 3KOR). Using the auxin-dependent reporter DR5:venus, a significant change in the auxin gradient toward the root tip was found in 3KO plants, which correlated with the loss of polar localization of the auxin transporter PIN1 in the stele and with the increased number of stele cells with oblique cell walls. Interestingly, myosin XI-K:YFP was localized to the cell division apparatus in the root and shoot meristems. In anaphase and early telophase, XI-K:YFP was concentrated in the midzone and the forming cell plate. In late telophase, XI-K:YFP formed a ring that overlapped with the growing phragmoplast. Myosin receptors MyoB1 and MyoB2 that are highly expressed throughout the plant were undetectable in dividing cells, suggesting that the myosin function in cell division relies on distinct adaptor proteins. These results suggest that myosin XIs are involved in orchestrating root organogenesis via effects on polar distribution of auxin responses and on cell division. Oxford University Press 2018-05-25 2018-03-22 /pmc/articles/PMC5972647/ /pubmed/29579267 http://dx.doi.org/10.1093/jxb/ery112 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Abu-Abied, Mohamad
Belausov, Eduard
Hagay, Sapir
Peremyslov, Valera
Dolja, Valerian
Sadot, Einat
Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title_full Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title_fullStr Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title_full_unstemmed Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title_short Myosin XI-K is involved in root organogenesis, polar auxin transport, and cell division
title_sort myosin xi-k is involved in root organogenesis, polar auxin transport, and cell division
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972647/
https://www.ncbi.nlm.nih.gov/pubmed/29579267
http://dx.doi.org/10.1093/jxb/ery112
work_keys_str_mv AT abuabiedmohamad myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision
AT belausoveduard myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision
AT hagaysapir myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision
AT peremyslovvalera myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision
AT doljavalerian myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision
AT sadoteinat myosinxikisinvolvedinrootorganogenesispolarauxintransportandcelldivision