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Overexpressed somatic alleles are enriched in functional elements in Breast Cancer
Asymmetric allele content in the transcriptome can be indicative of functional and selective features of the underlying genetic variants. Yet, imbalanced alleles, especially from diploid genome regions, are poorly explored in cancer. Here we systematically quantify and integrate the variant allele f...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557904/ https://www.ncbi.nlm.nih.gov/pubmed/28811643 http://dx.doi.org/10.1038/s41598-017-08416-w |
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author | Restrepo, Paula Movassagh, Mercedeh Alomran, Nawaf Miller, Christian Li, Muzi Trenkov, Chris Manchev, Yulian Bahl, Sonali Warnken, Stephanie Spurr, Liam Apanasovich, Tatiyana Crandall, Keith Edwards, Nathan Horvath, Anelia |
author_facet | Restrepo, Paula Movassagh, Mercedeh Alomran, Nawaf Miller, Christian Li, Muzi Trenkov, Chris Manchev, Yulian Bahl, Sonali Warnken, Stephanie Spurr, Liam Apanasovich, Tatiyana Crandall, Keith Edwards, Nathan Horvath, Anelia |
author_sort | Restrepo, Paula |
collection | PubMed |
description | Asymmetric allele content in the transcriptome can be indicative of functional and selective features of the underlying genetic variants. Yet, imbalanced alleles, especially from diploid genome regions, are poorly explored in cancer. Here we systematically quantify and integrate the variant allele fraction from corresponding RNA and DNA sequence data from patients with breast cancer acquired through The Cancer Genome Atlas (TCGA). We test for correlation between allele prevalence and functionality in known cancer-implicated genes from the Cancer Gene Census (CGC). We document significant allele-preferential expression of functional variants in CGC genes and across the entire dataset. Notably, we find frequent allele-specific overexpression of variants in tumor-suppressor genes. We also report a list of over-expressed variants from non-CGC genes. Overall, our analysis presents an integrated set of features of somatic allele expression and points to the vast information content of the asymmetric alleles in the cancer transcriptome. |
format | Online Article Text |
id | pubmed-5557904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55579042017-08-16 Overexpressed somatic alleles are enriched in functional elements in Breast Cancer Restrepo, Paula Movassagh, Mercedeh Alomran, Nawaf Miller, Christian Li, Muzi Trenkov, Chris Manchev, Yulian Bahl, Sonali Warnken, Stephanie Spurr, Liam Apanasovich, Tatiyana Crandall, Keith Edwards, Nathan Horvath, Anelia Sci Rep Article Asymmetric allele content in the transcriptome can be indicative of functional and selective features of the underlying genetic variants. Yet, imbalanced alleles, especially from diploid genome regions, are poorly explored in cancer. Here we systematically quantify and integrate the variant allele fraction from corresponding RNA and DNA sequence data from patients with breast cancer acquired through The Cancer Genome Atlas (TCGA). We test for correlation between allele prevalence and functionality in known cancer-implicated genes from the Cancer Gene Census (CGC). We document significant allele-preferential expression of functional variants in CGC genes and across the entire dataset. Notably, we find frequent allele-specific overexpression of variants in tumor-suppressor genes. We also report a list of over-expressed variants from non-CGC genes. Overall, our analysis presents an integrated set of features of somatic allele expression and points to the vast information content of the asymmetric alleles in the cancer transcriptome. Nature Publishing Group UK 2017-08-15 /pmc/articles/PMC5557904/ /pubmed/28811643 http://dx.doi.org/10.1038/s41598-017-08416-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Restrepo, Paula Movassagh, Mercedeh Alomran, Nawaf Miller, Christian Li, Muzi Trenkov, Chris Manchev, Yulian Bahl, Sonali Warnken, Stephanie Spurr, Liam Apanasovich, Tatiyana Crandall, Keith Edwards, Nathan Horvath, Anelia Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title | Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title_full | Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title_fullStr | Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title_full_unstemmed | Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title_short | Overexpressed somatic alleles are enriched in functional elements in Breast Cancer |
title_sort | overexpressed somatic alleles are enriched in functional elements in breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557904/ https://www.ncbi.nlm.nih.gov/pubmed/28811643 http://dx.doi.org/10.1038/s41598-017-08416-w |
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