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Derivation of consensus inactivation status for X-linked genes from genome-wide studies

BACKGROUND: X chromosome inactivation is the epigenetic silencing of the majority of the genes on one of the X chromosomes in XX therian mammals. In humans, approximately 15 % of genes consistently escape from this inactivation and another 15 % of genes vary between individuals or tissues in whether...

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Autores principales: Balaton, Bradley P., Cotton, Allison M., Brown, Carolyn J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696107/
https://www.ncbi.nlm.nih.gov/pubmed/26719789
http://dx.doi.org/10.1186/s13293-015-0053-7
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author Balaton, Bradley P.
Cotton, Allison M.
Brown, Carolyn J.
author_facet Balaton, Bradley P.
Cotton, Allison M.
Brown, Carolyn J.
author_sort Balaton, Bradley P.
collection PubMed
description BACKGROUND: X chromosome inactivation is the epigenetic silencing of the majority of the genes on one of the X chromosomes in XX therian mammals. In humans, approximately 15 % of genes consistently escape from this inactivation and another 15 % of genes vary between individuals or tissues in whether they are subject to, or escape from, inactivation. Multiple studies have provided inactivation status calls for a large subset of the genes on the X chromosome; however, these studies vary in which genes they were able to make calls for and in some cases which call they give a specific gene. METHODS: This analysis aggregated three published studies that have examined X chromosome inactivation status of genes across the X chromosome, generating consensus calls and identifying discordancies. The impact of expression level and chromosomal location on X chromosome inactivation status was also assessed. RESULTS: Overall, we assigned a consensus XCI status 639 genes, including 78 % of protein-coding genes expressed outside of the testes, with a lower frequency for non-coding RNA and testis-specific genes. Study-specific discordancies suggest that there may be instability of XCI during cell culture and also highlight study-specific variations in call type. We observe an enrichment of discordant genes at boundaries between genes subject to and escaping from inactivation. CONCLUSIONS: This study has compiled a comprehensive list of X-chromosome inactivation statuses for genes and also discovered some biases which will help guide future studies examining X-chromosome inactivation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-015-0053-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-46961072015-12-31 Derivation of consensus inactivation status for X-linked genes from genome-wide studies Balaton, Bradley P. Cotton, Allison M. Brown, Carolyn J. Biol Sex Differ Research BACKGROUND: X chromosome inactivation is the epigenetic silencing of the majority of the genes on one of the X chromosomes in XX therian mammals. In humans, approximately 15 % of genes consistently escape from this inactivation and another 15 % of genes vary between individuals or tissues in whether they are subject to, or escape from, inactivation. Multiple studies have provided inactivation status calls for a large subset of the genes on the X chromosome; however, these studies vary in which genes they were able to make calls for and in some cases which call they give a specific gene. METHODS: This analysis aggregated three published studies that have examined X chromosome inactivation status of genes across the X chromosome, generating consensus calls and identifying discordancies. The impact of expression level and chromosomal location on X chromosome inactivation status was also assessed. RESULTS: Overall, we assigned a consensus XCI status 639 genes, including 78 % of protein-coding genes expressed outside of the testes, with a lower frequency for non-coding RNA and testis-specific genes. Study-specific discordancies suggest that there may be instability of XCI during cell culture and also highlight study-specific variations in call type. We observe an enrichment of discordant genes at boundaries between genes subject to and escaping from inactivation. CONCLUSIONS: This study has compiled a comprehensive list of X-chromosome inactivation statuses for genes and also discovered some biases which will help guide future studies examining X-chromosome inactivation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-015-0053-7) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-30 /pmc/articles/PMC4696107/ /pubmed/26719789 http://dx.doi.org/10.1186/s13293-015-0053-7 Text en © Balaton et al. 2015 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 Research
Balaton, Bradley P.
Cotton, Allison M.
Brown, Carolyn J.
Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title_full Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title_fullStr Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title_full_unstemmed Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title_short Derivation of consensus inactivation status for X-linked genes from genome-wide studies
title_sort derivation of consensus inactivation status for x-linked genes from genome-wide studies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696107/
https://www.ncbi.nlm.nih.gov/pubmed/26719789
http://dx.doi.org/10.1186/s13293-015-0053-7
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