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Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis

BACKGROUND: Homoeologs are defined as homologous genes resulting from allopolyploidy. Bread wheat, Triticum aestivum, is an allohexaploid species with many homoeologs. Homoeolog expression bias, referring to the relative contribution of homoeologs to the transcriptome, is critical for determining th...

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Autores principales: Zhang, Lihua, He, Chao, Lai, Yuting, Wang, Yating, Kang, Lu, Liu, Ankui, Lan, Caixia, Su, Handong, Gao, Yuwen, Li, Zeqing, Yang, Fang, Li, Qiang, Mao, Hailiang, Chen, Dijun, Chen, Wei, Kaufmann, Kerstin, Yan, Wenhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074895/
https://www.ncbi.nlm.nih.gov/pubmed/37016448
http://dx.doi.org/10.1186/s13059-023-02908-x
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author Zhang, Lihua
He, Chao
Lai, Yuting
Wang, Yating
Kang, Lu
Liu, Ankui
Lan, Caixia
Su, Handong
Gao, Yuwen
Li, Zeqing
Yang, Fang
Li, Qiang
Mao, Hailiang
Chen, Dijun
Chen, Wei
Kaufmann, Kerstin
Yan, Wenhao
author_facet Zhang, Lihua
He, Chao
Lai, Yuting
Wang, Yating
Kang, Lu
Liu, Ankui
Lan, Caixia
Su, Handong
Gao, Yuwen
Li, Zeqing
Yang, Fang
Li, Qiang
Mao, Hailiang
Chen, Dijun
Chen, Wei
Kaufmann, Kerstin
Yan, Wenhao
author_sort Zhang, Lihua
collection PubMed
description BACKGROUND: Homoeologs are defined as homologous genes resulting from allopolyploidy. Bread wheat, Triticum aestivum, is an allohexaploid species with many homoeologs. Homoeolog expression bias, referring to the relative contribution of homoeologs to the transcriptome, is critical for determining the traits that influence wheat growth and development. Asymmetric transcription of homoeologs has been so far investigated in a tissue or organ-specific manner, which could be misleading due to a mixture of cell types. RESULTS: Here, we perform single nuclei RNA sequencing and ATAC sequencing of wheat root to study the asymmetric gene transcription, reconstruct cell differentiation trajectories and cell-type-specific gene regulatory networks. We identify 22 cell types. We then reconstruct cell differentiation trajectories that suggest different origins between epidermis/cortex and endodermis, distinguishing bread wheat from Arabidopsis. We show that the ratio of asymmetrically transcribed triads varies greatly when analyzing at the single-cell level. Hub transcription factors determining cell type identity are also identified. In particular, we demonstrate that TaSPL14 participates in vasculature development by regulating the expression of BAM1. Combining single-cell transcription and chromatin accessibility data, we construct the pseudo-time regulatory network driving root hair differentiation. We find MYB3R4, REF6, HDG1, and GATAs as key regulators in this process. CONCLUSIONS: Our findings reveal the transcriptional landscape of root organization and asymmetric gene transcription at single-cell resolution in polyploid wheat. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02908-x.
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spelling pubmed-100748952023-04-06 Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis Zhang, Lihua He, Chao Lai, Yuting Wang, Yating Kang, Lu Liu, Ankui Lan, Caixia Su, Handong Gao, Yuwen Li, Zeqing Yang, Fang Li, Qiang Mao, Hailiang Chen, Dijun Chen, Wei Kaufmann, Kerstin Yan, Wenhao Genome Biol Research BACKGROUND: Homoeologs are defined as homologous genes resulting from allopolyploidy. Bread wheat, Triticum aestivum, is an allohexaploid species with many homoeologs. Homoeolog expression bias, referring to the relative contribution of homoeologs to the transcriptome, is critical for determining the traits that influence wheat growth and development. Asymmetric transcription of homoeologs has been so far investigated in a tissue or organ-specific manner, which could be misleading due to a mixture of cell types. RESULTS: Here, we perform single nuclei RNA sequencing and ATAC sequencing of wheat root to study the asymmetric gene transcription, reconstruct cell differentiation trajectories and cell-type-specific gene regulatory networks. We identify 22 cell types. We then reconstruct cell differentiation trajectories that suggest different origins between epidermis/cortex and endodermis, distinguishing bread wheat from Arabidopsis. We show that the ratio of asymmetrically transcribed triads varies greatly when analyzing at the single-cell level. Hub transcription factors determining cell type identity are also identified. In particular, we demonstrate that TaSPL14 participates in vasculature development by regulating the expression of BAM1. Combining single-cell transcription and chromatin accessibility data, we construct the pseudo-time regulatory network driving root hair differentiation. We find MYB3R4, REF6, HDG1, and GATAs as key regulators in this process. CONCLUSIONS: Our findings reveal the transcriptional landscape of root organization and asymmetric gene transcription at single-cell resolution in polyploid wheat. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02908-x. BioMed Central 2023-04-04 /pmc/articles/PMC10074895/ /pubmed/37016448 http://dx.doi.org/10.1186/s13059-023-02908-x Text en © The Author(s) 2023 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
Zhang, Lihua
He, Chao
Lai, Yuting
Wang, Yating
Kang, Lu
Liu, Ankui
Lan, Caixia
Su, Handong
Gao, Yuwen
Li, Zeqing
Yang, Fang
Li, Qiang
Mao, Hailiang
Chen, Dijun
Chen, Wei
Kaufmann, Kerstin
Yan, Wenhao
Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title_full Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title_fullStr Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title_full_unstemmed Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title_short Asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
title_sort asymmetric gene expression and cell-type-specific regulatory networks in the root of bread wheat revealed by single-cell multiomics analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074895/
https://www.ncbi.nlm.nih.gov/pubmed/37016448
http://dx.doi.org/10.1186/s13059-023-02908-x
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