論文

査読有り 国際誌
2020年3月9日

Time-lapse single-cell transcriptomics reveals modulation of histone H3 for dormancy breaking in fission yeast.

Nature communications
  • Hayato Tsuyuzaki
  • ,
  • Masahito Hosokawa
  • ,
  • Koji Arikawa
  • ,
  • Takuya Yoda
  • ,
  • Naoyuki Okada
  • ,
  • Haruko Takeyama
  • ,
  • Masamitsu Sato

11
1
開始ページ
1265
終了ページ
1265
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41467-020-15060-y

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.

リンク情報
DOI
https://doi.org/10.1038/s41467-020-15060-y
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32152323
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062879
ID情報
  • DOI : 10.1038/s41467-020-15060-y
  • PubMed ID : 32152323
  • PubMed Central 記事ID : PMC7062879

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