Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.

Plant vascular meristems are sets of pluripotent cells that enable radial growth by giving rise to vascular tissues and are therefore crucial to plant development. However, the overall dynamics of cellular determination and patterning in and around vascular meristems is still unexplored. We study th...

Full description

Bibliographic Details
Main Authors: Mariana Benítez, Jan Hejátko
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23723973/?tool=EBI
id doaj-c7d66a24741f4551b44339721697ccb1
record_format Article
spelling doaj-c7d66a24741f4551b44339721697ccb12021-03-03T20:22:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0185e6310810.1371/journal.pone.0063108Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.Mariana BenítezJan HejátkoPlant vascular meristems are sets of pluripotent cells that enable radial growth by giving rise to vascular tissues and are therefore crucial to plant development. However, the overall dynamics of cellular determination and patterning in and around vascular meristems is still unexplored. We study this process in the shoot vascular tissue of Arabidopsis thaliana, which is organized in vascular bundles that contain three basic cell types (procambium, xylem and phloem). A set of molecules involved in this process has now been identified and partially characterized, but it is not yet clear how the regulatory interactions among them, in conjunction with cellular communication processes, give rise to the steady patterns that accompany cell-fate determination and arrangement within vascular bundles. We put forward a dynamic model factoring in the interactions between molecules (genes, peptides, mRNA and hormones) that have been reported to be central in this process, as well as the relevant communication mechanisms. When a few proposed interactions (unverified, but based on related data) are postulated, the model reproduces the hormonal and molecular patterns expected for the three regions within vascular bundles. In order to test the model, we simulated mutant and hormone-depleted systems and compared the results with experimentally reported phenotypes. The proposed model provides a formal framework integrating a set of growing experimental data and renders a dynamic account of how the collective action of hormones, genes, and other molecules may result in the specification of the three main cell types within shoot vascular bundles. It also offers a tool to test the necessity and sufficiency of particular interactions and conditions for vascular patterning and yields novel predictions that may be experimentally tested. Finally, this model provides a reference for further studies comparing the overall dynamics of tissue organization and formation by meristems in other plant organs and species.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23723973/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Mariana Benítez
Jan Hejátko
spellingShingle Mariana Benítez
Jan Hejátko
Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
PLoS ONE
author_facet Mariana Benítez
Jan Hejátko
author_sort Mariana Benítez
title Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
title_short Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
title_full Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
title_fullStr Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
title_full_unstemmed Dynamics of cell-fate determination and patterning in the vascular bundles of Arabidopsis thaliana.
title_sort dynamics of cell-fate determination and patterning in the vascular bundles of arabidopsis thaliana.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Plant vascular meristems are sets of pluripotent cells that enable radial growth by giving rise to vascular tissues and are therefore crucial to plant development. However, the overall dynamics of cellular determination and patterning in and around vascular meristems is still unexplored. We study this process in the shoot vascular tissue of Arabidopsis thaliana, which is organized in vascular bundles that contain three basic cell types (procambium, xylem and phloem). A set of molecules involved in this process has now been identified and partially characterized, but it is not yet clear how the regulatory interactions among them, in conjunction with cellular communication processes, give rise to the steady patterns that accompany cell-fate determination and arrangement within vascular bundles. We put forward a dynamic model factoring in the interactions between molecules (genes, peptides, mRNA and hormones) that have been reported to be central in this process, as well as the relevant communication mechanisms. When a few proposed interactions (unverified, but based on related data) are postulated, the model reproduces the hormonal and molecular patterns expected for the three regions within vascular bundles. In order to test the model, we simulated mutant and hormone-depleted systems and compared the results with experimentally reported phenotypes. The proposed model provides a formal framework integrating a set of growing experimental data and renders a dynamic account of how the collective action of hormones, genes, and other molecules may result in the specification of the three main cell types within shoot vascular bundles. It also offers a tool to test the necessity and sufficiency of particular interactions and conditions for vascular patterning and yields novel predictions that may be experimentally tested. Finally, this model provides a reference for further studies comparing the overall dynamics of tissue organization and formation by meristems in other plant organs and species.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23723973/?tool=EBI
work_keys_str_mv AT marianabenitez dynamicsofcellfatedeterminationandpatterninginthevascularbundlesofarabidopsisthaliana
AT janhejatko dynamicsofcellfatedeterminationandpatterninginthevascularbundlesofarabidopsisthaliana
_version_ 1714822788989059072