Cargando…
High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana
Female germline cells in flowering plants differentiate from somatic cells to produce specialized reproductive organs, called ovules, embedded deep inside the flowers. We investigated the molecular basis of this distinctive developmental program by performing single-cell RNA sequencing (scRNA-seq) o...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486858/ https://www.ncbi.nlm.nih.gov/pubmed/34599277 http://dx.doi.org/10.1038/s42003-021-02676-z |
_version_ | 1784577837754220544 |
---|---|
author | Hou, Zhimin Liu, Yanhui Zhang, Man Zhao, Lihua Jin, Xingyue Liu, Liping Su, Zhenxia Cai, Hanyang Qin, Yuan |
author_facet | Hou, Zhimin Liu, Yanhui Zhang, Man Zhao, Lihua Jin, Xingyue Liu, Liping Su, Zhenxia Cai, Hanyang Qin, Yuan |
author_sort | Hou, Zhimin |
collection | PubMed |
description | Female germline cells in flowering plants differentiate from somatic cells to produce specialized reproductive organs, called ovules, embedded deep inside the flowers. We investigated the molecular basis of this distinctive developmental program by performing single-cell RNA sequencing (scRNA-seq) of 16,872 single cells of Arabidopsis thaliana ovule primordia at three developmental time points during female germline differentiation. This allowed us to identify the characteristic expression patterns of the main cell types, including the female germline and its surrounding nucellus. We then reconstructed the continuous trajectory of female germline differentiation and observed dynamic waves of gene expression along the developmental trajectory. A focused analysis revealed transcriptional cascades and identified key transcriptional factors that showed distinct expression patterns along the germline differentiation trajectory. Our study provides a valuable reference dataset of the transcriptional process during female germline differentiation at single-cell resolution, shedding light on the mechanisms underlying germline cell fate determination. |
format | Online Article Text |
id | pubmed-8486858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84868582021-10-07 High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana Hou, Zhimin Liu, Yanhui Zhang, Man Zhao, Lihua Jin, Xingyue Liu, Liping Su, Zhenxia Cai, Hanyang Qin, Yuan Commun Biol Article Female germline cells in flowering plants differentiate from somatic cells to produce specialized reproductive organs, called ovules, embedded deep inside the flowers. We investigated the molecular basis of this distinctive developmental program by performing single-cell RNA sequencing (scRNA-seq) of 16,872 single cells of Arabidopsis thaliana ovule primordia at three developmental time points during female germline differentiation. This allowed us to identify the characteristic expression patterns of the main cell types, including the female germline and its surrounding nucellus. We then reconstructed the continuous trajectory of female germline differentiation and observed dynamic waves of gene expression along the developmental trajectory. A focused analysis revealed transcriptional cascades and identified key transcriptional factors that showed distinct expression patterns along the germline differentiation trajectory. Our study provides a valuable reference dataset of the transcriptional process during female germline differentiation at single-cell resolution, shedding light on the mechanisms underlying germline cell fate determination. Nature Publishing Group UK 2021-10-01 /pmc/articles/PMC8486858/ /pubmed/34599277 http://dx.doi.org/10.1038/s42003-021-02676-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hou, Zhimin Liu, Yanhui Zhang, Man Zhao, Lihua Jin, Xingyue Liu, Liping Su, Zhenxia Cai, Hanyang Qin, Yuan High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title | High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title_full | High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title_fullStr | High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title_full_unstemmed | High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title_short | High-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in Arabidopsis thaliana |
title_sort | high-throughput single-cell transcriptomics reveals the female germline differentiation trajectory in arabidopsis thaliana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486858/ https://www.ncbi.nlm.nih.gov/pubmed/34599277 http://dx.doi.org/10.1038/s42003-021-02676-z |
work_keys_str_mv | AT houzhimin highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT liuyanhui highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT zhangman highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT zhaolihua highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT jinxingyue highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT liuliping highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT suzhenxia highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT caihanyang highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana AT qinyuan highthroughputsinglecelltranscriptomicsrevealsthefemalegermlinedifferentiationtrajectoryinarabidopsisthaliana |