Uncovering dynamic transcriptional regulation of methanogenesis via single-cell imaging of archaeal gene expression

Archaeal methanogenesis is a dynamic process regulated by various cellular and environmental signals. However, understanding this regulation is technically challenging due to the difficulty of measuring gene expression dynamics in individual archaeal cells. Here, we develop a multi-round hybridization chain reaction (HCR)-assisted single-molecule fluorescence in situ hybridization (FISH) method to quantify the transcriptional dynamics of 12 genes involved in methanogenesis in individual cells of Methanococcoides orientis. Under optimal growth condition, most of these genes appear to be expressed in a temporal order matching metabolic reaction order. Interestingly, an important environmental factor, Fe(III), stimulates cellular methane production without upregulating methanogenic gene expression, likely through a Fenton-reaction-triggered mechanism. Through single-cell clustering and kinetic analyses, we associate these gene expression patterns to a dynamic mixture of distinct cellular states, potentially regulated by a set of shared factors. Our work provides a quantitative framework for uncovering the mechanisms of metabolic regulation in archaea.

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Publication Details

Journal
Nature Communications
Published
2025-03-06
DOI
https://doi.org/10.1038/s41467-025-57159-0
Citations
3
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
2.42

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article

Uncovering dynamic transcriptional regulation of methanogenesis via single-cell imaging of archaeal gene expression

Weishu Zhao, Fengping Wang, Heng Xu, Yijing Dong et al.
3 citations
Nature Communications
Single-cell and spatial transcriptomics
2.42
article

Uncovering dynamic transcriptional regulation of methanogenesis via single-cell imaging of archaeal gene expression

Weishu Zhao, Fengping Wang, Heng Xu, Yijing Dong, Lewen Liang, Jing Wang, Fei Zhao, Qi Li, Yifan Chen
article en
3 citations

Abstract

Archaeal methanogenesis is a dynamic process regulated by various cellular and environmental signals. However, understanding this regulation is technically challenging due to the difficulty of measuring gene expression dynamics in individual archaeal cells. Here, we develop a multi-round hybridization chain reaction (HCR)-assisted single-molecule fluorescence in situ hybridization (FISH) method to quantify the transcriptional dynamics of 12 genes involved in methanogenesis in individual cells of Methanococcoides orientis. Under optimal growth condition, most of these genes appear to be expressed in a temporal order matching metabolic reaction order. Interestingly, an important environmental factor, Fe(III), stimulates cellular methane production without upregulating methanogenic gene expression, likely through a Fenton-reaction-triggered mechanism. Through single-cell clustering and kinetic analyses, we associate these gene expression patterns to a dynamic mixture of distinct cellular states, potentially regulated by a set of shared factors. Our work provides a quantitative framework for uncovering the mechanisms of metabolic regulation in archaea.

Nature CommunicationsVol. 16(1)
Shanghai Jiao Tong University (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), Institute of Natural Science (KP), Shanghai Ocean University (CN)
Natural Science Foundation of Shanghai, National Natural Science Foundation of China
Openalex Percentile: Top 13%
Single-cell and spatial transcriptomics
2.42
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