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Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast
How quiescent cells break dormancy is a key issue in eukaryotic cells including cancer. Fungal spores, for example, remain quiescent for long periods until nourished, although the mechanisms by which dormancy is broken remain enigmatic. Transcriptome analysis could provide a clue, but methods to syn...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062879/ https://www.ncbi.nlm.nih.gov/pubmed/32152323 http://dx.doi.org/10.1038/s41467-020-15060-y |
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author | Tsuyuzaki, Hayato Hosokawa, Masahito Arikawa, Koji Yoda, Takuya Okada, Naoyuki Takeyama, Haruko Sato, Masamitsu |
author_facet | Tsuyuzaki, Hayato Hosokawa, Masahito Arikawa, Koji Yoda, Takuya Okada, Naoyuki Takeyama, Haruko Sato, Masamitsu |
author_sort | Tsuyuzaki, Hayato |
collection | PubMed |
description | How quiescent cells break dormancy is a key issue in eukaryotic cells including cancer. Fungal spores, for example, remain quiescent for long periods until nourished, although the mechanisms by which dormancy is broken remain enigmatic. Transcriptome analysis could provide a clue, but methods to synchronously germinate large numbers of spores are lacking, and thus it remains a challenge to analyse gene expression upon germination. Hence, we develop methods to assemble transcriptomes from individual, asynchronous spore cells of fission yeast undergoing germination to assess transcriptomic changes over time. The virtual time-lapse analyses highlights one of three copies of histone H3 genes whose transcription fluctuates during the initial stage of germination. Disruption of this temporal fluctuation causes defects in spore germination despite no visible defects in other stages of the life cycle. We conclude that modulation of histone H3 expression is a crucial ‘wake-up’ trigger at dormancy breaking. |
format | Online Article Text |
id | pubmed-7062879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70628792020-03-18 Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast Tsuyuzaki, Hayato Hosokawa, Masahito Arikawa, Koji Yoda, Takuya Okada, Naoyuki Takeyama, Haruko Sato, Masamitsu Nat Commun Article How quiescent cells break dormancy is a key issue in eukaryotic cells including cancer. Fungal spores, for example, remain quiescent for long periods until nourished, although the mechanisms by which dormancy is broken remain enigmatic. Transcriptome analysis could provide a clue, but methods to synchronously germinate large numbers of spores are lacking, and thus it remains a challenge to analyse gene expression upon germination. Hence, we develop methods to assemble transcriptomes from individual, asynchronous spore cells of fission yeast undergoing germination to assess transcriptomic changes over time. The virtual time-lapse analyses highlights one of three copies of histone H3 genes whose transcription fluctuates during the initial stage of germination. Disruption of this temporal fluctuation causes defects in spore germination despite no visible defects in other stages of the life cycle. We conclude that modulation of histone H3 expression is a crucial ‘wake-up’ trigger at dormancy breaking. Nature Publishing Group UK 2020-03-09 /pmc/articles/PMC7062879/ /pubmed/32152323 http://dx.doi.org/10.1038/s41467-020-15060-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Tsuyuzaki, Hayato Hosokawa, Masahito Arikawa, Koji Yoda, Takuya Okada, Naoyuki Takeyama, Haruko Sato, Masamitsu Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title | Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title_full | Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title_fullStr | Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title_full_unstemmed | Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title_short | Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast |
title_sort | time-lapse single-cell transcriptomics reveals modulation of histone h3 for dormancy breaking in fission yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062879/ https://www.ncbi.nlm.nih.gov/pubmed/32152323 http://dx.doi.org/10.1038/s41467-020-15060-y |
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