Cargando…
Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq
Plant defense responses involve several biological processes that allow plants to fight against pathogenic attacks. How these different processes are orchestrated within organs and depend on specific cell types is poorly known. Here, using single-cell RNA sequencing (scRNA-seq) technology on three i...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504604/ https://www.ncbi.nlm.nih.gov/pubmed/37644724 http://dx.doi.org/10.1016/j.xplc.2023.100676 |
_version_ | 1785106760744304640 |
---|---|
author | Delannoy, Etienne Batardiere, Bastien Pateyron, Stéphanie Soubigou-Taconnat, Ludivine Chiquet, Julien Colcombet, Jean Lang, Julien |
author_facet | Delannoy, Etienne Batardiere, Bastien Pateyron, Stéphanie Soubigou-Taconnat, Ludivine Chiquet, Julien Colcombet, Jean Lang, Julien |
author_sort | Delannoy, Etienne |
collection | PubMed |
description | Plant defense responses involve several biological processes that allow plants to fight against pathogenic attacks. How these different processes are orchestrated within organs and depend on specific cell types is poorly known. Here, using single-cell RNA sequencing (scRNA-seq) technology on three independent biological replicates, we identified several cell populations representing the core transcriptional responses of wild-type Arabidopsis leaves inoculated with the bacterial pathogen Pseudomonas syringae DC3000. Among these populations, we retrieved major cell types of the leaves (mesophyll, guard, epidermal, companion, and vascular S cells) with which we could associate characteristic transcriptional reprogramming and regulators, thereby specifying different cell-type responses to the pathogen. Further analyses of transcriptional dynamics, on the basis of inference of cell trajectories, indicated that the different cell types, in addition to their characteristic defense responses, can also share similar modules of gene reprogramming, uncovering a ubiquitous antagonism between immune and susceptible processes. Moreover, it appears that the defense responses of vascular S cells, epidermal cells, and mesophyll cells can evolve along two separate paths, one converging toward an identical cell fate, characterized mostly by lignification and detoxification functions. As this divergence does not correspond to the differentiation between immune and susceptible cells, we speculate that this might reflect the discrimination between cell-autonomous and non-cell-autonomous responses. Altogether our data provide an upgraded framework to describe, explore, and explain the specialization and the coordination of plant cell responses upon pathogenic challenge. |
format | Online Article Text |
id | pubmed-10504604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105046042023-09-17 Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq Delannoy, Etienne Batardiere, Bastien Pateyron, Stéphanie Soubigou-Taconnat, Ludivine Chiquet, Julien Colcombet, Jean Lang, Julien Plant Commun Research Article Plant defense responses involve several biological processes that allow plants to fight against pathogenic attacks. How these different processes are orchestrated within organs and depend on specific cell types is poorly known. Here, using single-cell RNA sequencing (scRNA-seq) technology on three independent biological replicates, we identified several cell populations representing the core transcriptional responses of wild-type Arabidopsis leaves inoculated with the bacterial pathogen Pseudomonas syringae DC3000. Among these populations, we retrieved major cell types of the leaves (mesophyll, guard, epidermal, companion, and vascular S cells) with which we could associate characteristic transcriptional reprogramming and regulators, thereby specifying different cell-type responses to the pathogen. Further analyses of transcriptional dynamics, on the basis of inference of cell trajectories, indicated that the different cell types, in addition to their characteristic defense responses, can also share similar modules of gene reprogramming, uncovering a ubiquitous antagonism between immune and susceptible processes. Moreover, it appears that the defense responses of vascular S cells, epidermal cells, and mesophyll cells can evolve along two separate paths, one converging toward an identical cell fate, characterized mostly by lignification and detoxification functions. As this divergence does not correspond to the differentiation between immune and susceptible cells, we speculate that this might reflect the discrimination between cell-autonomous and non-cell-autonomous responses. Altogether our data provide an upgraded framework to describe, explore, and explain the specialization and the coordination of plant cell responses upon pathogenic challenge. Elsevier 2023-08-28 /pmc/articles/PMC10504604/ /pubmed/37644724 http://dx.doi.org/10.1016/j.xplc.2023.100676 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Delannoy, Etienne Batardiere, Bastien Pateyron, Stéphanie Soubigou-Taconnat, Ludivine Chiquet, Julien Colcombet, Jean Lang, Julien Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title | Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title_full | Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title_fullStr | Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title_full_unstemmed | Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title_short | Cell specialization and coordination in Arabidopsis leaves upon pathogenic attack revealed by scRNA-seq |
title_sort | cell specialization and coordination in arabidopsis leaves upon pathogenic attack revealed by scrna-seq |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504604/ https://www.ncbi.nlm.nih.gov/pubmed/37644724 http://dx.doi.org/10.1016/j.xplc.2023.100676 |
work_keys_str_mv | AT delannoyetienne cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT batardierebastien cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT pateyronstephanie cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT soubigoutaconnatludivine cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT chiquetjulien cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT colcombetjean cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq AT langjulien cellspecializationandcoordinationinarabidopsisleavesuponpathogenicattackrevealedbyscrnaseq |