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Non-coding RNAs match the deleted genomic regions in humans

RNA is transcribed from DNA, and therefore, there should be no RNA transcript from the deleted DNA region. Our study attempted to analyse whether any RNA cache that maps the deleted regions is present in human cells. Using data from the 1000 genome project, we selected 41 CEPH (CEU) and 38 Yoruba (Y...

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Detalles Bibliográficos
Autores principales: Byeon, Boseon, Kovalchuk, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112596/
https://www.ncbi.nlm.nih.gov/pubmed/27853310
http://dx.doi.org/10.1038/srep37452
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author Byeon, Boseon
Kovalchuk, Igor
author_facet Byeon, Boseon
Kovalchuk, Igor
author_sort Byeon, Boseon
collection PubMed
description RNA is transcribed from DNA, and therefore, there should be no RNA transcript from the deleted DNA region. Our study attempted to analyse whether any RNA cache that maps the deleted regions is present in human cells. Using data from the 1000 genome project, we selected 41 CEPH (CEU) and 38 Yoruba (YRI) samples that included the data for the entire genome sequence and ncRNA and mRNA sequences. Aligning the ncRNA reads against the genomic DNA in individual samples has revealed that 229 out of 1114 homozygous deletions have ncRNA reads that map to them. Further analysis has revealed that ncRNA reads that map the deleted regions are enriched around the deletion ends and at genic regions of the genome. The read enrichment at deletion ends suggests that these ncRNAs are likely some form of double-strand break induced RNAs. Our analysis suggests that human cells may contain a residual ncRNA cache that is possibly propagated across generations.
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spelling pubmed-51125962016-11-25 Non-coding RNAs match the deleted genomic regions in humans Byeon, Boseon Kovalchuk, Igor Sci Rep Article RNA is transcribed from DNA, and therefore, there should be no RNA transcript from the deleted DNA region. Our study attempted to analyse whether any RNA cache that maps the deleted regions is present in human cells. Using data from the 1000 genome project, we selected 41 CEPH (CEU) and 38 Yoruba (YRI) samples that included the data for the entire genome sequence and ncRNA and mRNA sequences. Aligning the ncRNA reads against the genomic DNA in individual samples has revealed that 229 out of 1114 homozygous deletions have ncRNA reads that map to them. Further analysis has revealed that ncRNA reads that map the deleted regions are enriched around the deletion ends and at genic regions of the genome. The read enrichment at deletion ends suggests that these ncRNAs are likely some form of double-strand break induced RNAs. Our analysis suggests that human cells may contain a residual ncRNA cache that is possibly propagated across generations. Nature Publishing Group 2016-11-17 /pmc/articles/PMC5112596/ /pubmed/27853310 http://dx.doi.org/10.1038/srep37452 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Byeon, Boseon
Kovalchuk, Igor
Non-coding RNAs match the deleted genomic regions in humans
title Non-coding RNAs match the deleted genomic regions in humans
title_full Non-coding RNAs match the deleted genomic regions in humans
title_fullStr Non-coding RNAs match the deleted genomic regions in humans
title_full_unstemmed Non-coding RNAs match the deleted genomic regions in humans
title_short Non-coding RNAs match the deleted genomic regions in humans
title_sort non-coding rnas match the deleted genomic regions in humans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112596/
https://www.ncbi.nlm.nih.gov/pubmed/27853310
http://dx.doi.org/10.1038/srep37452
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