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Defining the criteria for identifying constitutional epimutations
In the January 2016 issue of Clinical Epigenetics, Quiñonez-Silva et al. (Clin Epigenetics 8:1, 2016) described a possible constitutional epimutation of the RB1 gene as a cause of hereditary predisposition to retinoblastoma. The term constitutional epimutation describes an epigenetic aberration in n...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835913/ https://www.ncbi.nlm.nih.gov/pubmed/27096027 http://dx.doi.org/10.1186/s13148-016-0207-4 |
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author | Sloane, Mathew A. Ward, Robyn L. Hesson, Luke B. |
author_facet | Sloane, Mathew A. Ward, Robyn L. Hesson, Luke B. |
author_sort | Sloane, Mathew A. |
collection | PubMed |
description | In the January 2016 issue of Clinical Epigenetics, Quiñonez-Silva et al. (Clin Epigenetics 8:1, 2016) described a possible constitutional epimutation of the RB1 gene as a cause of hereditary predisposition to retinoblastoma. The term constitutional epimutation describes an epigenetic aberration in normal tissues that predisposes to disease. The data presented by Quiñonez-Silva et al. are interesting, but further analysis is required to demonstrate a constitutional epimutation in this family. Here, we define the criteria and describe the experimental approach necessary to identify an epigenetic aberration as a constitutional epimutation. |
format | Online Article Text |
id | pubmed-4835913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48359132016-04-20 Defining the criteria for identifying constitutional epimutations Sloane, Mathew A. Ward, Robyn L. Hesson, Luke B. Clin Epigenetics Letter to the Editor In the January 2016 issue of Clinical Epigenetics, Quiñonez-Silva et al. (Clin Epigenetics 8:1, 2016) described a possible constitutional epimutation of the RB1 gene as a cause of hereditary predisposition to retinoblastoma. The term constitutional epimutation describes an epigenetic aberration in normal tissues that predisposes to disease. The data presented by Quiñonez-Silva et al. are interesting, but further analysis is required to demonstrate a constitutional epimutation in this family. Here, we define the criteria and describe the experimental approach necessary to identify an epigenetic aberration as a constitutional epimutation. BioMed Central 2016-04-18 /pmc/articles/PMC4835913/ /pubmed/27096027 http://dx.doi.org/10.1186/s13148-016-0207-4 Text en © Sloane et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Letter to the Editor Sloane, Mathew A. Ward, Robyn L. Hesson, Luke B. Defining the criteria for identifying constitutional epimutations |
title | Defining the criteria for identifying constitutional epimutations |
title_full | Defining the criteria for identifying constitutional epimutations |
title_fullStr | Defining the criteria for identifying constitutional epimutations |
title_full_unstemmed | Defining the criteria for identifying constitutional epimutations |
title_short | Defining the criteria for identifying constitutional epimutations |
title_sort | defining the criteria for identifying constitutional epimutations |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835913/ https://www.ncbi.nlm.nih.gov/pubmed/27096027 http://dx.doi.org/10.1186/s13148-016-0207-4 |
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