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Isolation and analysis of rereplicated DNA by Rerep-Seq

Changes in gene copy number contribute to genomic instability, the onset and progression of cancer, developmental abnormalities and adaptive potential. The origins of gene amplifications have remained elusive; however, DNA rereplication has been implicated as a source of gene amplifications. The ina...

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Autores principales: Menzel, Johannes, Tatman, Philip, Black, Joshua C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261181/
https://www.ncbi.nlm.nih.gov/pubmed/32239215
http://dx.doi.org/10.1093/nar/gkaa197
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author Menzel, Johannes
Tatman, Philip
Black, Joshua C
author_facet Menzel, Johannes
Tatman, Philip
Black, Joshua C
author_sort Menzel, Johannes
collection PubMed
description Changes in gene copy number contribute to genomic instability, the onset and progression of cancer, developmental abnormalities and adaptive potential. The origins of gene amplifications have remained elusive; however, DNA rereplication has been implicated as a source of gene amplifications. The inability to determine which sequences are rereplicated and under what conditions have made it difficult to determine the validity of the proposed models. Here we present Rerep-Seq, a technique that selectively enriches for rereplicated DNA in preparation for analysis by DNA sequencing that can be applied to any species. We validated Rerep-Seq by simulating DNA rereplication in yeast and human cells. Using Rerep-Seq, we demonstrate that rereplication induced in Saccharomyces cerevisiae by deregulated origin licensing is non-random and defined by broad domains that span multiple replication origins and topological boundaries.
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spelling pubmed-72611812020-06-03 Isolation and analysis of rereplicated DNA by Rerep-Seq Menzel, Johannes Tatman, Philip Black, Joshua C Nucleic Acids Res Methods Online Changes in gene copy number contribute to genomic instability, the onset and progression of cancer, developmental abnormalities and adaptive potential. The origins of gene amplifications have remained elusive; however, DNA rereplication has been implicated as a source of gene amplifications. The inability to determine which sequences are rereplicated and under what conditions have made it difficult to determine the validity of the proposed models. Here we present Rerep-Seq, a technique that selectively enriches for rereplicated DNA in preparation for analysis by DNA sequencing that can be applied to any species. We validated Rerep-Seq by simulating DNA rereplication in yeast and human cells. Using Rerep-Seq, we demonstrate that rereplication induced in Saccharomyces cerevisiae by deregulated origin licensing is non-random and defined by broad domains that span multiple replication origins and topological boundaries. Oxford University Press 2020-06-04 2020-04-02 /pmc/articles/PMC7261181/ /pubmed/32239215 http://dx.doi.org/10.1093/nar/gkaa197 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 Methods Online
Menzel, Johannes
Tatman, Philip
Black, Joshua C
Isolation and analysis of rereplicated DNA by Rerep-Seq
title Isolation and analysis of rereplicated DNA by Rerep-Seq
title_full Isolation and analysis of rereplicated DNA by Rerep-Seq
title_fullStr Isolation and analysis of rereplicated DNA by Rerep-Seq
title_full_unstemmed Isolation and analysis of rereplicated DNA by Rerep-Seq
title_short Isolation and analysis of rereplicated DNA by Rerep-Seq
title_sort isolation and analysis of rereplicated dna by rerep-seq
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261181/
https://www.ncbi.nlm.nih.gov/pubmed/32239215
http://dx.doi.org/10.1093/nar/gkaa197
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