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Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus

Callus is a reprogrammed cell mass involved in plant regeneration and gene transformation in crop engineering. Pluripotent callus cells develop into fertile shoots through shoot regeneration. The molecular basis of the shoot regeneration process in crop callus remains largely elusive. This study pio...

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Autores principales: Song, Xiehai, Guo, Pengru, Xia, Keke, Wang, Meiling, Liu, Yongqi, Chen, Lichuan, Zhang, Jinhui, Xu, Mengyuan, Liu, Naixu, Yue, Zhiliang, Xu, Xun, Gu, Ying, Li, Gang, Liu, Min, Fang, Liang, Deng, Xing Wang, Li, Bosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515167/
https://www.ncbi.nlm.nih.gov/pubmed/37703282
http://dx.doi.org/10.1073/pnas.2310163120
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author Song, Xiehai
Guo, Pengru
Xia, Keke
Wang, Meiling
Liu, Yongqi
Chen, Lichuan
Zhang, Jinhui
Xu, Mengyuan
Liu, Naixu
Yue, Zhiliang
Xu, Xun
Gu, Ying
Li, Gang
Liu, Min
Fang, Liang
Deng, Xing Wang
Li, Bosheng
author_facet Song, Xiehai
Guo, Pengru
Xia, Keke
Wang, Meiling
Liu, Yongqi
Chen, Lichuan
Zhang, Jinhui
Xu, Mengyuan
Liu, Naixu
Yue, Zhiliang
Xu, Xun
Gu, Ying
Li, Gang
Liu, Min
Fang, Liang
Deng, Xing Wang
Li, Bosheng
author_sort Song, Xiehai
collection PubMed
description Callus is a reprogrammed cell mass involved in plant regeneration and gene transformation in crop engineering. Pluripotent callus cells develop into fertile shoots through shoot regeneration. The molecular basis of the shoot regeneration process in crop callus remains largely elusive. This study pioneers the exploration of the spatial transcriptome of tomato callus during shoot regeneration. The findings reveal the presence of highly heterogeneous cell populations within the callus, including epidermis, vascular tissue, shoot primordia, inner callus, and outgrowth shoots. By characterizing the spatially resolved molecular features of shoot primordia and surrounding cells, specific factors essential for shoot primordia formation are identified. Notably, chlorenchyma cells, enriched in photosynthesis-related processes, play a crucial role in promoting shoot primordia formation and subsequent shoot regeneration. Light is shown to promote shoot regeneration by inducing chlorenchyma cell development and coordinating sugar signaling. These findings significantly advance our understanding of the cellular and molecular aspects of shoot regeneration in tomato callus and demonstrate the immense potential of spatial transcriptomics in plant biology.
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spelling pubmed-105151672023-09-23 Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus Song, Xiehai Guo, Pengru Xia, Keke Wang, Meiling Liu, Yongqi Chen, Lichuan Zhang, Jinhui Xu, Mengyuan Liu, Naixu Yue, Zhiliang Xu, Xun Gu, Ying Li, Gang Liu, Min Fang, Liang Deng, Xing Wang Li, Bosheng Proc Natl Acad Sci U S A Biological Sciences Callus is a reprogrammed cell mass involved in plant regeneration and gene transformation in crop engineering. Pluripotent callus cells develop into fertile shoots through shoot regeneration. The molecular basis of the shoot regeneration process in crop callus remains largely elusive. This study pioneers the exploration of the spatial transcriptome of tomato callus during shoot regeneration. The findings reveal the presence of highly heterogeneous cell populations within the callus, including epidermis, vascular tissue, shoot primordia, inner callus, and outgrowth shoots. By characterizing the spatially resolved molecular features of shoot primordia and surrounding cells, specific factors essential for shoot primordia formation are identified. Notably, chlorenchyma cells, enriched in photosynthesis-related processes, play a crucial role in promoting shoot primordia formation and subsequent shoot regeneration. Light is shown to promote shoot regeneration by inducing chlorenchyma cell development and coordinating sugar signaling. These findings significantly advance our understanding of the cellular and molecular aspects of shoot regeneration in tomato callus and demonstrate the immense potential of spatial transcriptomics in plant biology. National Academy of Sciences 2023-09-13 2023-09-19 /pmc/articles/PMC10515167/ /pubmed/37703282 http://dx.doi.org/10.1073/pnas.2310163120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Song, Xiehai
Guo, Pengru
Xia, Keke
Wang, Meiling
Liu, Yongqi
Chen, Lichuan
Zhang, Jinhui
Xu, Mengyuan
Liu, Naixu
Yue, Zhiliang
Xu, Xun
Gu, Ying
Li, Gang
Liu, Min
Fang, Liang
Deng, Xing Wang
Li, Bosheng
Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title_full Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title_fullStr Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title_full_unstemmed Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title_short Spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
title_sort spatial transcriptomics reveals light-induced chlorenchyma cells involved in promoting shoot regeneration in tomato callus
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515167/
https://www.ncbi.nlm.nih.gov/pubmed/37703282
http://dx.doi.org/10.1073/pnas.2310163120
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