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Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle
In plants, a complex mixture of solutes and macromolecules is transported by the phloem. Here, we examined how solutes and macromolecules are separated when they exit the phloem during the unloading process. We used a combination of approaches (non-invasive imaging, 3D-electron microscopy, and mathe...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365319/ https://www.ncbi.nlm.nih.gov/pubmed/28230527 http://dx.doi.org/10.7554/eLife.24125 |
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author | Ross-Elliott, Timothy J Jensen, Kaare H Haaning, Katrine S Wager, Brittney M Knoblauch, Jan Howell, Alexander H Mullendore, Daniel L Monteith, Alexander G Paultre, Danae Yan, Dawei Otero, Sofia Bourdon, Matthieu Sager, Ross Lee, Jung-Youn Helariutta, Ykä Knoblauch, Michael Oparka, Karl J |
author_facet | Ross-Elliott, Timothy J Jensen, Kaare H Haaning, Katrine S Wager, Brittney M Knoblauch, Jan Howell, Alexander H Mullendore, Daniel L Monteith, Alexander G Paultre, Danae Yan, Dawei Otero, Sofia Bourdon, Matthieu Sager, Ross Lee, Jung-Youn Helariutta, Ykä Knoblauch, Michael Oparka, Karl J |
author_sort | Ross-Elliott, Timothy J |
collection | PubMed |
description | In plants, a complex mixture of solutes and macromolecules is transported by the phloem. Here, we examined how solutes and macromolecules are separated when they exit the phloem during the unloading process. We used a combination of approaches (non-invasive imaging, 3D-electron microscopy, and mathematical modelling) to show that phloem unloading of solutes in Arabidopsis roots occurs through plasmodesmata by a combination of mass flow and diffusion (convective phloem unloading). During unloading, solutes and proteins are diverted into the phloem-pole pericycle, a tissue connected to the protophloem by a unique class of ‘funnel plasmodesmata’. While solutes are unloaded without restriction, large proteins are released through funnel plasmodesmata in discrete pulses, a phenomenon we refer to as ‘batch unloading’. Unlike solutes, these proteins remain restricted to the phloem-pole pericycle. Our data demonstrate a major role for the phloem-pole pericycle in regulating phloem unloading in roots. DOI: http://dx.doi.org/10.7554/eLife.24125.001 |
format | Online Article Text |
id | pubmed-5365319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53653192017-03-27 Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle Ross-Elliott, Timothy J Jensen, Kaare H Haaning, Katrine S Wager, Brittney M Knoblauch, Jan Howell, Alexander H Mullendore, Daniel L Monteith, Alexander G Paultre, Danae Yan, Dawei Otero, Sofia Bourdon, Matthieu Sager, Ross Lee, Jung-Youn Helariutta, Ykä Knoblauch, Michael Oparka, Karl J eLife Plant Biology In plants, a complex mixture of solutes and macromolecules is transported by the phloem. Here, we examined how solutes and macromolecules are separated when they exit the phloem during the unloading process. We used a combination of approaches (non-invasive imaging, 3D-electron microscopy, and mathematical modelling) to show that phloem unloading of solutes in Arabidopsis roots occurs through plasmodesmata by a combination of mass flow and diffusion (convective phloem unloading). During unloading, solutes and proteins are diverted into the phloem-pole pericycle, a tissue connected to the protophloem by a unique class of ‘funnel plasmodesmata’. While solutes are unloaded without restriction, large proteins are released through funnel plasmodesmata in discrete pulses, a phenomenon we refer to as ‘batch unloading’. Unlike solutes, these proteins remain restricted to the phloem-pole pericycle. Our data demonstrate a major role for the phloem-pole pericycle in regulating phloem unloading in roots. DOI: http://dx.doi.org/10.7554/eLife.24125.001 eLife Sciences Publications, Ltd 2017-02-23 /pmc/articles/PMC5365319/ /pubmed/28230527 http://dx.doi.org/10.7554/eLife.24125 Text en © 2017, Ross-Elliott et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Plant Biology Ross-Elliott, Timothy J Jensen, Kaare H Haaning, Katrine S Wager, Brittney M Knoblauch, Jan Howell, Alexander H Mullendore, Daniel L Monteith, Alexander G Paultre, Danae Yan, Dawei Otero, Sofia Bourdon, Matthieu Sager, Ross Lee, Jung-Youn Helariutta, Ykä Knoblauch, Michael Oparka, Karl J Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title | Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title_full | Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title_fullStr | Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title_full_unstemmed | Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title_short | Phloem unloading in Arabidopsis roots is convective and regulated by the phloem-pole pericycle |
title_sort | phloem unloading in arabidopsis roots is convective and regulated by the phloem-pole pericycle |
topic | Plant Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365319/ https://www.ncbi.nlm.nih.gov/pubmed/28230527 http://dx.doi.org/10.7554/eLife.24125 |
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