Evidence map›Paper›PMID 40050284›Full record

ArticleNature communications2025

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

Yijing Dong, Lanting Qi, Fei Zhao, Yifan Chen, Lewen Liang, Jing Wang, Weishu Zhao, Fengping Wang, Heng Xu

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yijing DongSchool of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0002-9553-8481
Lanting QiSchool of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai, China.
Fei ZhaoSchool of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai, China.
Yifan ChenState Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0003-3542-878X
Lewen LiangKey Laboratory of Polar Ecosystem and Climate Change, Ministry of Education, and School of Oceanography, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0002-6951-5382
Jing WangKey Laboratory of Polar Ecosystem and Climate Change, Ministry of Education, and School of Oceanography, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0003-0547-6780
Weishu ZhaoState Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.ORCID http://orcid.org/0000-0002-0753-8300
Fengping WangState Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China. fengpingw@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-3429-8410
Heng XuSchool of Physics and Astronomy, Shanghai Jiao Tong University, Shanghai, China. Heng_Xu@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-3717-0412

Funding

National Natural Science Foundation of China (National Science Foundation of China) 11774225National Natural Science Foundation of China (National Science Foundation of China) 12474194National Natural Science Foundation of China (National Science Foundation of China) 41921006National Natural Science Foundation of China (National Science Foundation of China) 42230401National Natural Science Foundation of China (National Science Foundation of China) 42406089Natural Science Foundation of Shanghai (Natural Science Foundation of Shanghai Municipality) 22ZR1434000
6 · The paper itself

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.

Indexed as

Gene Expression Regulation, ArchaealMethaneSingle-Cell AnalysisTranscription, GeneticArchaeaArchaeal ProteinsIn Situ Hybridization, FluorescenceArchaeal ProteinsMethane

Identifiers

PMID40050284
PMCPMC11885431

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.