Evidence map›Paper›PMID 31613873›Full record

ArticlePLoS biology2019

Experimental evolution reveals a general role for the methyltransferase Hmt1 in noise buffering.

Shu-Ting You, Yu-Ting Jhou, Cheng-Fu Kao, Jun-Yi Leu

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. bioRxiv : the preprint server for biology · 2025
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  8. How is epigenetics predicted to contribute to climate change adaptation? What evidence do we need?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    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

4 authors at 2 institutions in 1 country.

Shu-Ting YouMolecular and Cell Biology, Taiwan International Graduate Program, Graduate Institute of Life Sciences, National Defense Medical Center and Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-4581-9568
Yu-Ting JhouInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0001-7438-8069
Cheng-Fu KaoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Jun-Yi LeuMolecular and Cell Biology, Taiwan International Graduate Program, Graduate Institute of Life Sciences, National Defense Medical Center and Academia Sinica, Taipei, Taiwan.ORCID 0000-0001-5445-2799
Institute of Molecular Biology, Academia Sinica · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-to-cell heterogeneity within an isogenic population has been observed in prokaryotic and eukaryotic cells. Such heterogeneity often manifests at the level of individual protein abundance and may have evolutionary benefits, especially for organisms in fluctuating environments. Although general features and the origins of cellular noise have been revealed, details of the molecular pathways underlying noise regulation remain elusive. Here, we used experimental evolution of Saccharomyces cerevisiae to select for mutations that increase reporter protein noise. By combining bulk segregant analysis and CRISPR/Cas9-based reconstitution, we identified the methyltransferase Hmt1 as a general regulator of noise buffering. Hmt1 methylation activity is critical for the evolved phenotype, and we also show that two of the Hmt1 methylation targets can suppress noise. Hmt1 functions as an environmental sensor to adjust noise levels in response to environmental cues. Moreover, Hmt1-mediated noise buffering is conserved in an evolutionarily distant yeast species, suggesting broad significance of noise regulation.

Indexed as

Gene Expression Regulation, FungalGenetic HeterogeneityProtein Processing, Post-TranslationalCRISPR-Cas SystemsDirected Molecular EvolutionEthyl MethanesulfonateGene EditingGenes, ReporterGlyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)Green Fluorescent ProteinsMethylationMutationProtein-Arginine N-MethyltransferasesRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsEthyl MethanesulfonateGlyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)Green Fluorescent ProteinsHMT1 protein, S cerevisiaeProtein-Arginine N-MethyltransferasesRepressor ProteinsSaccharomyces cerevisiae ProteinsTDH2 protein, S cerevisiae

Identifiers

PMID31613873
PMCPMC6814240
OpenAlexW2980584128

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.