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

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. W...

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Autores principales: Prada-Luengo, Iñigo, Møller, Henrik D, Henriksen, Rasmus A, Gao, Qian, Larsen, Camilla Eggert, Alizadeh, Sefa, Maretty, Lasse, Houseley, Jonathan, Regenberg, Birgitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430651/
https://www.ncbi.nlm.nih.gov/pubmed/32609810
http://dx.doi.org/10.1093/nar/gkaa545
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author Prada-Luengo, Iñigo
Møller, Henrik D
Henriksen, Rasmus A
Gao, Qian
Larsen, Camilla Eggert
Alizadeh, Sefa
Maretty, Lasse
Houseley, Jonathan
Regenberg, Birgitte
author_facet Prada-Luengo, Iñigo
Møller, Henrik D
Henriksen, Rasmus A
Gao, Qian
Larsen, Camilla Eggert
Alizadeh, Sefa
Maretty, Lasse
Houseley, Jonathan
Regenberg, Birgitte
author_sort Prada-Luengo, Iñigo
collection PubMed
description 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: [HXT6/7(circle)] 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, [HXT6/7(circle)] 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.
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spelling pubmed-74306512020-08-19 Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae Prada-Luengo, Iñigo Møller, Henrik D Henriksen, Rasmus A Gao, Qian Larsen, Camilla Eggert Alizadeh, Sefa Maretty, Lasse Houseley, Jonathan Regenberg, Birgitte Nucleic Acids Res Genomics 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: [HXT6/7(circle)] 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, [HXT6/7(circle)] 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. Oxford University Press 2020-07-01 /pmc/articles/PMC7430651/ /pubmed/32609810 http://dx.doi.org/10.1093/nar/gkaa545 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Prada-Luengo, Iñigo
Møller, Henrik D
Henriksen, Rasmus A
Gao, Qian
Larsen, Camilla Eggert
Alizadeh, Sefa
Maretty, Lasse
Houseley, Jonathan
Regenberg, Birgitte
Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title_full Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title_fullStr Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title_full_unstemmed Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title_short Replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular DNA in Saccharomyces cerevisiae
title_sort replicative aging is associated with loss of genetic heterogeneity from extrachromosomal circular dna in saccharomyces cerevisiae
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430651/
https://www.ncbi.nlm.nih.gov/pubmed/32609810
http://dx.doi.org/10.1093/nar/gkaa545
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