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Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes

Commonly-mutated genes have been found for many cancers, but less is known about mutations in cis-regulatory elements. We leverage gains in tumor-specific enhancer activity, coupled with allele-biased mutation detection from H3K27ac ChIP-seq data, to pinpoint potential enhancer-activating mutations...

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Autores principales: Hung, Stevephen, Saiakhova, Alina, Faber, Zachary J, Bartels, Cynthia F, Neu, Devin, Bayles, Ian, Ojo, Evelyn, Hong, Ellen S, Pontius, W Dean, Morton, Andrew R, Liu, Ruifu, Kalady, Matthew F, Wald, David N, Markowitz, Sanford, Scacheri, Peter C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374075/
https://www.ncbi.nlm.nih.gov/pubmed/30759065
http://dx.doi.org/10.7554/eLife.40760
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author Hung, Stevephen
Saiakhova, Alina
Faber, Zachary J
Bartels, Cynthia F
Neu, Devin
Bayles, Ian
Ojo, Evelyn
Hong, Ellen S
Pontius, W Dean
Morton, Andrew R
Liu, Ruifu
Kalady, Matthew F
Wald, David N
Markowitz, Sanford
Scacheri, Peter C
author_facet Hung, Stevephen
Saiakhova, Alina
Faber, Zachary J
Bartels, Cynthia F
Neu, Devin
Bayles, Ian
Ojo, Evelyn
Hong, Ellen S
Pontius, W Dean
Morton, Andrew R
Liu, Ruifu
Kalady, Matthew F
Wald, David N
Markowitz, Sanford
Scacheri, Peter C
author_sort Hung, Stevephen
collection PubMed
description Commonly-mutated genes have been found for many cancers, but less is known about mutations in cis-regulatory elements. We leverage gains in tumor-specific enhancer activity, coupled with allele-biased mutation detection from H3K27ac ChIP-seq data, to pinpoint potential enhancer-activating mutations in colorectal cancer (CRC). Analysis of a genetically-diverse cohort of CRC specimens revealed that microsatellite instable (MSI) samples have a high indel rate within active enhancers. Enhancers with indels show evidence of positive selection, increased target gene expression, and a subset is highly recurrent. The indels affect short homopolymer tracts of A/T and increase affinity for FOX transcription factors. We further demonstrate that signature mismatch-repair (MMR) mutations activate enhancers using a xenograft tumor metastasis model, where mutations are induced naturally via CRISPR/Cas9 inactivation of MLH1 prior to tumor cell injection. Our results suggest that MMR signature mutations activate enhancers in CRC tumor epigenomes to provide a selective advantage.
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spelling pubmed-63740752019-02-15 Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes Hung, Stevephen Saiakhova, Alina Faber, Zachary J Bartels, Cynthia F Neu, Devin Bayles, Ian Ojo, Evelyn Hong, Ellen S Pontius, W Dean Morton, Andrew R Liu, Ruifu Kalady, Matthew F Wald, David N Markowitz, Sanford Scacheri, Peter C eLife Cancer Biology Commonly-mutated genes have been found for many cancers, but less is known about mutations in cis-regulatory elements. We leverage gains in tumor-specific enhancer activity, coupled with allele-biased mutation detection from H3K27ac ChIP-seq data, to pinpoint potential enhancer-activating mutations in colorectal cancer (CRC). Analysis of a genetically-diverse cohort of CRC specimens revealed that microsatellite instable (MSI) samples have a high indel rate within active enhancers. Enhancers with indels show evidence of positive selection, increased target gene expression, and a subset is highly recurrent. The indels affect short homopolymer tracts of A/T and increase affinity for FOX transcription factors. We further demonstrate that signature mismatch-repair (MMR) mutations activate enhancers using a xenograft tumor metastasis model, where mutations are induced naturally via CRISPR/Cas9 inactivation of MLH1 prior to tumor cell injection. Our results suggest that MMR signature mutations activate enhancers in CRC tumor epigenomes to provide a selective advantage. eLife Sciences Publications, Ltd 2019-02-13 /pmc/articles/PMC6374075/ /pubmed/30759065 http://dx.doi.org/10.7554/eLife.40760 Text en © 2019, Hung et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cancer Biology
Hung, Stevephen
Saiakhova, Alina
Faber, Zachary J
Bartels, Cynthia F
Neu, Devin
Bayles, Ian
Ojo, Evelyn
Hong, Ellen S
Pontius, W Dean
Morton, Andrew R
Liu, Ruifu
Kalady, Matthew F
Wald, David N
Markowitz, Sanford
Scacheri, Peter C
Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title_full Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title_fullStr Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title_full_unstemmed Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title_short Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
title_sort mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374075/
https://www.ncbi.nlm.nih.gov/pubmed/30759065
http://dx.doi.org/10.7554/eLife.40760
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