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Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing

Extrachromosomal (ec) DNA in eukaryotic cells has been known for decades. The structures described range from linear double stranded (ds) DNA to circular dsDNA, distinct from mitochondrial (mt) DNA. The sizes of circular forms are described from some hundred base pairs (bp) up to more than 150 kbp....

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Autor principal: Dennin, Reinhard H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Penerbit Universiti Sains Malaysia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422590/
https://www.ncbi.nlm.nih.gov/pubmed/30918452
http://dx.doi.org/10.21315/mjms2018.25.2.3
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author Dennin, Reinhard H
author_facet Dennin, Reinhard H
author_sort Dennin, Reinhard H
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description Extrachromosomal (ec) DNA in eukaryotic cells has been known for decades. The structures described range from linear double stranded (ds) DNA to circular dsDNA, distinct from mitochondrial (mt) DNA. The sizes of circular forms are described from some hundred base pairs (bp) up to more than 150 kbp. The number of molecules per cell ranges from several hundred to a thousand. Semi-quantitative determinations of circular dsDNA show proportions as high as several percentages of the total DNA per cell. These ecDNA fractions harbor sequences that are known to be present in chromosomal DNA (chrDNA) too. Sequencing projects on, for example the human genome, have to take into account the ecDNA sequences which are simultaneously ascertained; corrections cannot be performed retrospectively. Concerning the results of sequencings derived from extracted whole DNA: if the ecDNA fractions contained therein are not taken into account, erroneous conclusions at the chromosomal level may result.
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spelling pubmed-64225902019-03-27 Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing Dennin, Reinhard H Malays J Med Sci Review Article Extrachromosomal (ec) DNA in eukaryotic cells has been known for decades. The structures described range from linear double stranded (ds) DNA to circular dsDNA, distinct from mitochondrial (mt) DNA. The sizes of circular forms are described from some hundred base pairs (bp) up to more than 150 kbp. The number of molecules per cell ranges from several hundred to a thousand. Semi-quantitative determinations of circular dsDNA show proportions as high as several percentages of the total DNA per cell. These ecDNA fractions harbor sequences that are known to be present in chromosomal DNA (chrDNA) too. Sequencing projects on, for example the human genome, have to take into account the ecDNA sequences which are simultaneously ascertained; corrections cannot be performed retrospectively. Concerning the results of sequencings derived from extracted whole DNA: if the ecDNA fractions contained therein are not taken into account, erroneous conclusions at the chromosomal level may result. Penerbit Universiti Sains Malaysia 2018-03 2018-04-27 /pmc/articles/PMC6422590/ /pubmed/30918452 http://dx.doi.org/10.21315/mjms2018.25.2.3 Text en © Penerbit Universiti Sains Malaysia, 2018 This work is licensed under the terms of the Creative Commons Attribution (CC BY) (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Dennin, Reinhard H
Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title_full Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title_fullStr Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title_full_unstemmed Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title_short Overlooked: Extrachromosomal DNA and Their Possible Impact on Whole Genome Sequencing
title_sort overlooked: extrachromosomal dna and their possible impact on whole genome sequencing
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422590/
https://www.ncbi.nlm.nih.gov/pubmed/30918452
http://dx.doi.org/10.21315/mjms2018.25.2.3
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