Evidence map›Paper›PMID 33022053›Full record

ArticleMolecular biology and evolution2021

Long-Term m5C Methylome Dynamics Parallel Phenotypic Adaptation in the Cyanobacterium Trichodesmium.

Nathan G Walworth, Michael D Lee, Egor Dolzhenko, Fei-Xue Fu, Andrew D Smith, Eric A Webb, David A Hutchins

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Dual thermal ecotypes coexist within a nearly genetically identical population of the unicellular marine cyanobacteriumProceedings of the National Academy of Sciences of the United States of America · 2023
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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

7 authors at 2 institutions in 1 country.

Nathan G WalworthDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
Michael D LeeExobiology Branch, NASA Ames Research Center, Mountain View, CA, USA.
Egor DolzhenkoDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
Fei-Xue FuDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
Andrew D SmithDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
Eric A WebbDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
David A HutchinsDepartment of Biological Sciences, University of Southern California, Los Angeles, CA, USA.
University of Southern California · USAmes Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major challenge in modern biology is understanding how the effects of short-term biological responses influence long-term evolutionary adaptation, defined as a genetically determined increase in fitness to novel environments. This is particularly important in globally important microbes experiencing rapid global change, due to their influence on food webs, biogeochemical cycles, and climate. Epigenetic modifications like methylation have been demonstrated to influence short-term plastic responses, which ultimately impact long-term adaptive responses to environmental change. However, there remains a paucity of empirical research examining long-term methylation dynamics during environmental adaptation in nonmodel, ecologically important microbes. Here, we show the first empirical evidence in a marine prokaryote for long-term m5C methylome modifications correlated with phenotypic adaptation to CO2, using a 7-year evolution experiment (1,000+ generations) with the biogeochemically important marine cyanobacterium Trichodesmium. We identify m5C methylated sites that rapidly changed in response to high (750 µatm) CO2 exposure and were maintained for at least 4.5 years of CO2 selection. After 7 years of CO2 selection, however, m5C methylation levels that initially responded to high-CO2 returned to ancestral, ambient CO2 levels. Concurrently, high-CO2 adapted growth and N2 fixation rates remained significantly higher than those of ambient CO2 adapted cell lines irrespective of CO2 concentration, a trend consistent with genetic assimilation theory. These data demonstrate the maintenance of CO2-responsive m5C methylation for 4.5 years alongside phenotypic adaptation before returning to ancestral methylation levels. These observations in a globally distributed marine prokaryote provide critical evolutionary insights into biogeochemically important traits under global change.

Indexed as

Adaptation, BiologicalBiological EvolutionDNA MethylationCarbon DioxideEpigenomePhenotypeTranscription, GeneticTrichodesmiumCarbon Dioxideglobal changemarine microbiologymethylationmicrobial evolutionnitrogen fixationocean acidification

Identifiers

PMID33022053
PMCPMC7947765
OpenAlexW3092155090

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LicenceCC BY-NC
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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.