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The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues

In the developing seeds of all higher plants, filial cells are symplastically isolated from the maternal tissue supplying photosynthate to the reproductive structure. Photoassimilates must be transported apoplastically, crossing several membrane barriers, a process facilitated by sugar transporters....

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Autores principales: Chen, Lily, Ganguly, Diep R, Shafik, Sarah H, Danila, Florence, Grof, Christopher P L, Sharwood, Robert E, Furbank, Robert T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560085/
https://www.ncbi.nlm.nih.gov/pubmed/36883216
http://dx.doi.org/10.1093/jxb/erad076
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author Chen, Lily
Ganguly, Diep R
Shafik, Sarah H
Danila, Florence
Grof, Christopher P L
Sharwood, Robert E
Furbank, Robert T
author_facet Chen, Lily
Ganguly, Diep R
Shafik, Sarah H
Danila, Florence
Grof, Christopher P L
Sharwood, Robert E
Furbank, Robert T
author_sort Chen, Lily
collection PubMed
description In the developing seeds of all higher plants, filial cells are symplastically isolated from the maternal tissue supplying photosynthate to the reproductive structure. Photoassimilates must be transported apoplastically, crossing several membrane barriers, a process facilitated by sugar transporters. Sugars Will Eventually be Exported Transporters (SWEETs) have been proposed to play a crucial role in apoplastic sugar transport during phloem unloading and the post-phloem pathway in sink tissues. Evidence for this is presented here for developing seeds of the C(4) model grass Setaria viridis. Using immunolocalization, SvSWEET4 was detected in various maternal and filial tissues within the seed along the sugar transport pathway, in the vascular parenchyma of the pedicel, and in the xylem parenchyma of the stem. Expression of SvSWEET4a in Xenopus laevis oocytes indicated that it functions as a high-capacity glucose and sucrose transporter. Carbohydrate and transcriptional profiling of Setaria seed heads showed that there were some developmental shifts in hexose and sucrose content and consistent expression of SvSWEET4 homologues. Collectively, these results provide evidence for the involvement of SWEETs in the apoplastic transport pathway of sink tissues and allow a pathway for post-phloem sugar transport into the seed to be proposed.
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spelling pubmed-105600852023-10-08 The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues Chen, Lily Ganguly, Diep R Shafik, Sarah H Danila, Florence Grof, Christopher P L Sharwood, Robert E Furbank, Robert T J Exp Bot Research Papers In the developing seeds of all higher plants, filial cells are symplastically isolated from the maternal tissue supplying photosynthate to the reproductive structure. Photoassimilates must be transported apoplastically, crossing several membrane barriers, a process facilitated by sugar transporters. Sugars Will Eventually be Exported Transporters (SWEETs) have been proposed to play a crucial role in apoplastic sugar transport during phloem unloading and the post-phloem pathway in sink tissues. Evidence for this is presented here for developing seeds of the C(4) model grass Setaria viridis. Using immunolocalization, SvSWEET4 was detected in various maternal and filial tissues within the seed along the sugar transport pathway, in the vascular parenchyma of the pedicel, and in the xylem parenchyma of the stem. Expression of SvSWEET4a in Xenopus laevis oocytes indicated that it functions as a high-capacity glucose and sucrose transporter. Carbohydrate and transcriptional profiling of Setaria seed heads showed that there were some developmental shifts in hexose and sucrose content and consistent expression of SvSWEET4 homologues. Collectively, these results provide evidence for the involvement of SWEETs in the apoplastic transport pathway of sink tissues and allow a pathway for post-phloem sugar transport into the seed to be proposed. Oxford University Press 2023-03-08 /pmc/articles/PMC10560085/ /pubmed/36883216 http://dx.doi.org/10.1093/jxb/erad076 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://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
Chen, Lily
Ganguly, Diep R
Shafik, Sarah H
Danila, Florence
Grof, Christopher P L
Sharwood, Robert E
Furbank, Robert T
The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title_full The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title_fullStr The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title_full_unstemmed The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title_short The role of SWEET4 proteins in the post-phloem sugar transport pathway of Setaria viridis sink tissues
title_sort role of sweet4 proteins in the post-phloem sugar transport pathway of setaria viridis sink tissues
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560085/
https://www.ncbi.nlm.nih.gov/pubmed/36883216
http://dx.doi.org/10.1093/jxb/erad076
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