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Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf

BACKGROUND: The developmental gradient in monocot leaves has been exploited to uncover leaf developmental gene expression programs and chloroplast biogenesis processes. However, the relationship between the two is barely understood, which limits the value of transcriptome data to understand the proc...

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Autores principales: Loudya, Naresh, Mishra, Priyanka, Takahagi, Kotaro, Uehara-Yamaguchi, Yukiko, Inoue, Komaki, Bogre, Laszlo, Mochida, Keiichi, López-Juez, Enrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111775/
https://www.ncbi.nlm.nih.gov/pubmed/33975629
http://dx.doi.org/10.1186/s13059-021-02366-3
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author Loudya, Naresh
Mishra, Priyanka
Takahagi, Kotaro
Uehara-Yamaguchi, Yukiko
Inoue, Komaki
Bogre, Laszlo
Mochida, Keiichi
López-Juez, Enrique
author_facet Loudya, Naresh
Mishra, Priyanka
Takahagi, Kotaro
Uehara-Yamaguchi, Yukiko
Inoue, Komaki
Bogre, Laszlo
Mochida, Keiichi
López-Juez, Enrique
author_sort Loudya, Naresh
collection PubMed
description BACKGROUND: The developmental gradient in monocot leaves has been exploited to uncover leaf developmental gene expression programs and chloroplast biogenesis processes. However, the relationship between the two is barely understood, which limits the value of transcriptome data to understand the process of chloroplast development. RESULTS: Taking advantage of the developmental gradient in the bread wheat leaf, we provide a simultaneous quantitative analysis for the development of mesophyll cells and of chloroplasts as a cellular compartment. This allows us to generate the first biologically-informed gene expression map of this leaf, with the entire developmental gradient from meristematic to fully differentiated cells captured. We show that the first phase of plastid development begins with organelle proliferation, which extends well beyond cell proliferation, and continues with the establishment and then the build-up of the plastid genetic machinery. The second phase is marked by the development of photosynthetic chloroplasts which occupy the available cellular space. Using a network reconstruction algorithm, we predict that known chloroplast gene expression regulators are differentially involved across those developmental stages. CONCLUSIONS: Our analysis generates both the first wheat leaf transcriptional map and one of the most comprehensive descriptions to date of the developmental history of chloroplasts in higher plants. It reveals functionally distinct plastid and chloroplast development stages, identifies processes occurring in each of them, and highlights our very limited knowledge of the earliest drivers of plastid biogenesis, while providing a basis for their future identification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02366-3.
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spelling pubmed-81117752021-05-11 Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf Loudya, Naresh Mishra, Priyanka Takahagi, Kotaro Uehara-Yamaguchi, Yukiko Inoue, Komaki Bogre, Laszlo Mochida, Keiichi López-Juez, Enrique Genome Biol Research BACKGROUND: The developmental gradient in monocot leaves has been exploited to uncover leaf developmental gene expression programs and chloroplast biogenesis processes. However, the relationship between the two is barely understood, which limits the value of transcriptome data to understand the process of chloroplast development. RESULTS: Taking advantage of the developmental gradient in the bread wheat leaf, we provide a simultaneous quantitative analysis for the development of mesophyll cells and of chloroplasts as a cellular compartment. This allows us to generate the first biologically-informed gene expression map of this leaf, with the entire developmental gradient from meristematic to fully differentiated cells captured. We show that the first phase of plastid development begins with organelle proliferation, which extends well beyond cell proliferation, and continues with the establishment and then the build-up of the plastid genetic machinery. The second phase is marked by the development of photosynthetic chloroplasts which occupy the available cellular space. Using a network reconstruction algorithm, we predict that known chloroplast gene expression regulators are differentially involved across those developmental stages. CONCLUSIONS: Our analysis generates both the first wheat leaf transcriptional map and one of the most comprehensive descriptions to date of the developmental history of chloroplasts in higher plants. It reveals functionally distinct plastid and chloroplast development stages, identifies processes occurring in each of them, and highlights our very limited knowledge of the earliest drivers of plastid biogenesis, while providing a basis for their future identification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02366-3. BioMed Central 2021-05-11 /pmc/articles/PMC8111775/ /pubmed/33975629 http://dx.doi.org/10.1186/s13059-021-02366-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Loudya, Naresh
Mishra, Priyanka
Takahagi, Kotaro
Uehara-Yamaguchi, Yukiko
Inoue, Komaki
Bogre, Laszlo
Mochida, Keiichi
López-Juez, Enrique
Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title_full Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title_fullStr Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title_full_unstemmed Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title_short Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
title_sort cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111775/
https://www.ncbi.nlm.nih.gov/pubmed/33975629
http://dx.doi.org/10.1186/s13059-021-02366-3
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