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Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves
C4 photosynthesis in the maize leaf involves the exchange of organic acids between mesophyll (M) and the bundle sheath (BS) cells. The transport is mediated by plasmodesmata embedded in the suberized cell wall. We examined the maize Kranz anatomy with a focus on the plasmodesmata and cell wall suber...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943126/ https://www.ncbi.nlm.nih.gov/pubmed/35322159 http://dx.doi.org/10.1038/s41598-022-09135-7 |
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author | Gao, Peng Wang, Pengfei Du, Baijuan Li, Pinghua Kang, Byung-Ho |
author_facet | Gao, Peng Wang, Pengfei Du, Baijuan Li, Pinghua Kang, Byung-Ho |
author_sort | Gao, Peng |
collection | PubMed |
description | C4 photosynthesis in the maize leaf involves the exchange of organic acids between mesophyll (M) and the bundle sheath (BS) cells. The transport is mediated by plasmodesmata embedded in the suberized cell wall. We examined the maize Kranz anatomy with a focus on the plasmodesmata and cell wall suberization with microscopy methods. In the young leaf zone where M and BS cells had indistinguishable proplastids, plasmodesmata were simple and no suberin was detected. In leaf zones where dimorphic chloroplasts were evident, the plasmodesma acquired sphincter and cytoplasmic sleeves, and suberin was discerned. These modifications were accompanied by a drop in symplastic dye mobility at the M-BS boundary. We compared the kinetics of chloroplast differentiation and the modifications in M-BS connectivity in ppdk and dct2 mutants where C4 cycle is affected. The rate of chloroplast diversification did not alter, but plasmodesma remodeling, symplastic transport inhibition, and cell wall suberization were observed from younger leaf zone in the mutants than in wild type. Our results indicate that inactivation of the C4 genes accelerated the changes in the M-BS interface, and the reduced permeability suggests that symplastic transport between M and BS could be regulated for normal operation of C4 cycle. |
format | Online Article Text |
id | pubmed-8943126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89431262022-03-28 Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves Gao, Peng Wang, Pengfei Du, Baijuan Li, Pinghua Kang, Byung-Ho Sci Rep Article C4 photosynthesis in the maize leaf involves the exchange of organic acids between mesophyll (M) and the bundle sheath (BS) cells. The transport is mediated by plasmodesmata embedded in the suberized cell wall. We examined the maize Kranz anatomy with a focus on the plasmodesmata and cell wall suberization with microscopy methods. In the young leaf zone where M and BS cells had indistinguishable proplastids, plasmodesmata were simple and no suberin was detected. In leaf zones where dimorphic chloroplasts were evident, the plasmodesma acquired sphincter and cytoplasmic sleeves, and suberin was discerned. These modifications were accompanied by a drop in symplastic dye mobility at the M-BS boundary. We compared the kinetics of chloroplast differentiation and the modifications in M-BS connectivity in ppdk and dct2 mutants where C4 cycle is affected. The rate of chloroplast diversification did not alter, but plasmodesma remodeling, symplastic transport inhibition, and cell wall suberization were observed from younger leaf zone in the mutants than in wild type. Our results indicate that inactivation of the C4 genes accelerated the changes in the M-BS interface, and the reduced permeability suggests that symplastic transport between M and BS could be regulated for normal operation of C4 cycle. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943126/ /pubmed/35322159 http://dx.doi.org/10.1038/s41598-022-09135-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gao, Peng Wang, Pengfei Du, Baijuan Li, Pinghua Kang, Byung-Ho Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title | Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title_full | Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title_fullStr | Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title_full_unstemmed | Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title_short | Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves |
title_sort | accelerated remodeling of the mesophyll-bundle sheath interface in the maize c4 cycle mutant leaves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943126/ https://www.ncbi.nlm.nih.gov/pubmed/35322159 http://dx.doi.org/10.1038/s41598-022-09135-7 |
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