Evidence map›Paper›PMID 32609810›Full record

ArticleNucleic acids research2020

Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae.

Iñigo Prada-Luengo, Henrik D Møller, Rasmus A Henriksen, Qian Gao, Camilla Eggert Larsen, Sefa Alizadeh, Lasse Maretty, Jonathan Houseley, Birgitte Regenberg

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  17. Variation of extrachromosomal circular DNA in cancer cell lines.Computational and structural biotechnology journal · 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

9 authors at 3 institutions in 3 countries.

Iñigo Prada-LuengoEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
Henrik D MøllerEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
Rasmus A HenriksenEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
Qian GaoEpigenetics Programme, The Babraham Institute, Babraham, Cambridge CB22 3-AT, UK.
Camilla Eggert LarsenEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
Sefa AlizadehEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
Lasse MarettyDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus DK-8200, Denmark.
Jonathan HouseleyEpigenetics Programme, The Babraham Institute, Babraham, Cambridge CB22 3-AT, UK.
Birgitte RegenbergEcology and Evolution, Department of Biology, University of Copenhagen, Copenhagen DK-2100, Denmark.
University of Copenhagen · DKBabraham Institute · GBAarhus University Hospital · DK

Funding

Wellcome Trust 088335Wellcome Trust 110216
6 · The paper itself

Abstract

Circular DNA can arise from all parts of eukaryotic chromosomes. In yeast, circular ribosomal DNA (rDNA) accumulates dramatically as cells age, however little is known about the accumulation of other chromosome-derived circles or the contribution of such circles to genetic variation in aged cells. We profiled circular DNA in Saccharomyces cerevisiae populations sampled when young and after extensive aging. Young cells possessed highly diverse circular DNA populations but 94% of the circular DNA were lost after ∼15 divisions, whereas rDNA circles underwent massive accumulation to >95% of circular DNA. Circles present in both young and old cells were characterized by replication origins including circles from unique regions of the genome and repetitive regions: rDNA and telomeric Y' regions. We further observed that circles can have flexible inheritance patterns: [HXT6/7circle] normally segregates to mother cells but in low glucose is present in up to 50% of cells, the majority of which must have inherited this circle from their mother. Interestingly, [HXT6/7circle] cells are eventually replaced by cells carrying stable chromosomal HXT6 HXT6/7 HXT7 amplifications, suggesting circular DNAs are intermediates in chromosomal amplifications. In conclusion, the heterogeneity of circular DNA offers flexibility in adaptation, but this heterogeneity is remarkably diminished with age.

Indexed as

DNA ReplicationCellular SenescenceDNA, CircularGenetic VariationInheritance PatternsMonosaccharide Transport ProteinsRepetitive Sequences, Nucleic AcidReplication OriginSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsDNA, CircularHxt6 protein, S cerevisiaeHXT7 protein, S cerevisiaeMonosaccharide Transport ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID32609810
PMCPMC7430651
OpenAlexW3040517865

What OpenQuestion holds

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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.