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Transcriptional landscape of highly lignified poplar stems at single-cell resolution

BACKGROUND: Plant secondary growth depends on the activity of the vascular cambium, which produces xylem and phloem. Wood derived from xylem is the most abundant form of biomass globally and has played key socio-economic and subsistence roles throughout human history. However, despite intensive stud...

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Autores principales: Chen, Yang, Tong, Shaofei, Jiang, Yuanzhong, Ai, Fandi, Feng, Yanlin, Zhang, Junlin, Gong, Jue, Qin, Jiajia, Zhang, Yuanyuan, Zhu, Yingying, Liu, Jianquan, Ma, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607660/
https://www.ncbi.nlm.nih.gov/pubmed/34809675
http://dx.doi.org/10.1186/s13059-021-02537-2
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author Chen, Yang
Tong, Shaofei
Jiang, Yuanzhong
Ai, Fandi
Feng, Yanlin
Zhang, Junlin
Gong, Jue
Qin, Jiajia
Zhang, Yuanyuan
Zhu, Yingying
Liu, Jianquan
Ma, Tao
author_facet Chen, Yang
Tong, Shaofei
Jiang, Yuanzhong
Ai, Fandi
Feng, Yanlin
Zhang, Junlin
Gong, Jue
Qin, Jiajia
Zhang, Yuanyuan
Zhu, Yingying
Liu, Jianquan
Ma, Tao
author_sort Chen, Yang
collection PubMed
description BACKGROUND: Plant secondary growth depends on the activity of the vascular cambium, which produces xylem and phloem. Wood derived from xylem is the most abundant form of biomass globally and has played key socio-economic and subsistence roles throughout human history. However, despite intensive study of vascular development, the full diversity of cell types and the gene networks engaged are still poorly understood. RESULTS: Here, we have applied an optimized protoplast isolation protocol and RNA sequencing to characterize the high-resolution single-cell transcriptional landscape of highly lignified poplar stems. We identify 20 putative cell clusters with a series of novel cluster-specific marker genes and find that these cells are highly heterogeneous based on the transcriptome. Analysis of these marker genes’ expression dynamics enables reconstruction of the cell differentiation trajectories involved in phloem and xylem development. We find that different cell clusters exhibit distinct patterns of phytohormone responses and emphasize the use of our data to predict potential gene redundancy and identify candidate genes related to vascular development in trees. CONCLUSIONS: These findings establish the transcriptional landscape of major cell types of poplar stems at single-cell resolution and provide a valuable resource for investigating basic principles of vascular cell specification and differentiation in trees. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02537-2.
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spelling pubmed-86076602021-11-22 Transcriptional landscape of highly lignified poplar stems at single-cell resolution Chen, Yang Tong, Shaofei Jiang, Yuanzhong Ai, Fandi Feng, Yanlin Zhang, Junlin Gong, Jue Qin, Jiajia Zhang, Yuanyuan Zhu, Yingying Liu, Jianquan Ma, Tao Genome Biol Research BACKGROUND: Plant secondary growth depends on the activity of the vascular cambium, which produces xylem and phloem. Wood derived from xylem is the most abundant form of biomass globally and has played key socio-economic and subsistence roles throughout human history. However, despite intensive study of vascular development, the full diversity of cell types and the gene networks engaged are still poorly understood. RESULTS: Here, we have applied an optimized protoplast isolation protocol and RNA sequencing to characterize the high-resolution single-cell transcriptional landscape of highly lignified poplar stems. We identify 20 putative cell clusters with a series of novel cluster-specific marker genes and find that these cells are highly heterogeneous based on the transcriptome. Analysis of these marker genes’ expression dynamics enables reconstruction of the cell differentiation trajectories involved in phloem and xylem development. We find that different cell clusters exhibit distinct patterns of phytohormone responses and emphasize the use of our data to predict potential gene redundancy and identify candidate genes related to vascular development in trees. CONCLUSIONS: These findings establish the transcriptional landscape of major cell types of poplar stems at single-cell resolution and provide a valuable resource for investigating basic principles of vascular cell specification and differentiation in trees. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-021-02537-2. BioMed Central 2021-11-22 /pmc/articles/PMC8607660/ /pubmed/34809675 http://dx.doi.org/10.1186/s13059-021-02537-2 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
Chen, Yang
Tong, Shaofei
Jiang, Yuanzhong
Ai, Fandi
Feng, Yanlin
Zhang, Junlin
Gong, Jue
Qin, Jiajia
Zhang, Yuanyuan
Zhu, Yingying
Liu, Jianquan
Ma, Tao
Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title_full Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title_fullStr Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title_full_unstemmed Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title_short Transcriptional landscape of highly lignified poplar stems at single-cell resolution
title_sort transcriptional landscape of highly lignified poplar stems at single-cell resolution
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607660/
https://www.ncbi.nlm.nih.gov/pubmed/34809675
http://dx.doi.org/10.1186/s13059-021-02537-2
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