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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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