Evidence map›Paper›PMID 34133727›Full record

ArticleNucleic acids research2021

Cytosine base modifications regulate DNA duplex stability and metabolism.

Cathia Rausch, Peng Zhang, Corella S Casas-Delucchi, Julia L Daiß, Christoph Engel, Gideon Coster, Florian D Hastert, Patrick Weber, M Cristina Cardoso

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  12. Epigenetic control of tetrapyrrole biosynthesis by m4C DNA methylation in a cyanobacterium.DNA research : an international journal for rapid publication of reports on genes and genomes · 2024
    Article
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  16. Review
  17. Article
  18. Article
  19. Review
  20. G-quadruplex formation at humanBiochemistry and biophysics reports · 2023
    Article
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 at 4 institutions in 3 countries.

Cathia RauschCell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Peng ZhangCell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Corella S Casas-DelucchiChester Beatty Laboratories, The Institute of Cancer Research, London SW3 6JB, UK.
Julia L DaißRegensburg Center for Biochemistry, University of Regensburg, 93053 Regensburg, Germany.
Christoph EngelRegensburg Center for Biochemistry, University of Regensburg, 93053 Regensburg, Germany.ORCID 0000-0001-8451-3599
Gideon CosterChester Beatty Laboratories, The Institute of Cancer Research, London SW3 6JB, UK.
Florian D HastertCell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.ORCID 0000-0001-9961-5766
Patrick WeberCell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.
M Cristina CardosoCell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.ORCID 0000-0001-8427-8859
Technische Universität Darmstadt · DEInstitute of Cancer Research · GBUniversity of Regensburg · DEGuiyang Medical University · CN

Funding

Wellcome Trust 210470/Z/18/Z
6 · The paper itself

Abstract

DNA base modifications diversify the genome and are essential players in development. Yet, their influence on DNA physical properties and the ensuing effects on genome metabolism are poorly understood. Here, we focus on the interplay of cytosine modifications and DNA processes. We show by a combination of in vitro reactions with well-defined protein compositions and conditions, and in vivo experiments within the complex networks of the cell that cytosine methylation stabilizes the DNA helix, increasing its melting temperature and reducing DNA helicase and RNA/DNA polymerase speed. Oxidation of methylated cytosine, however, reverts the duplex stabilizing and genome metabolic effects to the level of unmodified cytosine. We detect this effect with DNA replication and transcription proteins originating from different species, ranging from prokaryotic and viral to the eukaryotic yeast and mammalian proteins. Accordingly, lack of cytosine methylation increases replication fork speed by enhancing DNA helicase unwinding speed in cells. We further validate that this cannot simply be explained by altered global DNA decondensation, changes in histone marks or chromatin structure and accessibility. We propose that the variegated deposition of cytosine modifications along the genome regulates DNA helix stability, thereby providing an elementary mechanism for local fine-tuning of DNA metabolism.

Indexed as

AnimalsBase PairingCell CycleCell LineCells, CulturedCytosineDNADNA-Directed DNA PolymeraseDNA-Directed RNA PolymerasesDNA HelicasesDNA ReplicationGenomic InstabilityHEK293 CellsHumansIn Situ Hybridization, FluorescenceMethylationCytosineDNADNA-Directed DNA PolymeraseDNA-Directed RNA PolymerasesDNA Helicases

Identifiers

PMID34133727
PMCPMC8682791
OpenAlexW3167328193

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.