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Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures
Transgenic rodent (TGR) models use bacterial reporter genes to quantify in vivo mutagenesis. Pairing TGR assays with next-generation sequencing (NGS) enables comprehensive mutation pattern analysis to inform mutational mechanisms. We used this approach to identify 2751 independent lacZ mutations in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429849/ https://www.ncbi.nlm.nih.gov/pubmed/32796912 http://dx.doi.org/10.1038/s42003-020-01174-y |
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author | Beal, Marc A. Meier, Matthew J. LeBlanc, Danielle P. Maurice, Clotilde O’Brien, Jason M. Yauk, Carole L. Marchetti, Francesco |
author_facet | Beal, Marc A. Meier, Matthew J. LeBlanc, Danielle P. Maurice, Clotilde O’Brien, Jason M. Yauk, Carole L. Marchetti, Francesco |
author_sort | Beal, Marc A. |
collection | PubMed |
description | Transgenic rodent (TGR) models use bacterial reporter genes to quantify in vivo mutagenesis. Pairing TGR assays with next-generation sequencing (NGS) enables comprehensive mutation pattern analysis to inform mutational mechanisms. We used this approach to identify 2751 independent lacZ mutations in the bone marrow of MutaMouse animals exposed to four chemical mutagens: benzo[a]pyrene, N-ethyl-N-nitrosourea, procarbazine, and triethylenemelamine. We also collected published data for 706 lacZ mutations from eight additional environmental mutagens. We report that lacZ gene sequencing generates chemical-specific mutation signatures observed in human cancers with established environmental causes. For example, the mutation signature of benzo[a]pyrene, a carcinogen present in tobacco smoke, matched the signature associated with tobacco-induced lung cancers. Our results suggest that the analysis of chemically induced mutations in the lacZ gene shortly after exposure provides an effective approach to characterize human-relevant mechanisms of carcinogenesis and propose novel environmental causes of mutation signatures observed in human cancers. |
format | Online Article Text |
id | pubmed-7429849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74298492020-08-27 Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures Beal, Marc A. Meier, Matthew J. LeBlanc, Danielle P. Maurice, Clotilde O’Brien, Jason M. Yauk, Carole L. Marchetti, Francesco Commun Biol Article Transgenic rodent (TGR) models use bacterial reporter genes to quantify in vivo mutagenesis. Pairing TGR assays with next-generation sequencing (NGS) enables comprehensive mutation pattern analysis to inform mutational mechanisms. We used this approach to identify 2751 independent lacZ mutations in the bone marrow of MutaMouse animals exposed to four chemical mutagens: benzo[a]pyrene, N-ethyl-N-nitrosourea, procarbazine, and triethylenemelamine. We also collected published data for 706 lacZ mutations from eight additional environmental mutagens. We report that lacZ gene sequencing generates chemical-specific mutation signatures observed in human cancers with established environmental causes. For example, the mutation signature of benzo[a]pyrene, a carcinogen present in tobacco smoke, matched the signature associated with tobacco-induced lung cancers. Our results suggest that the analysis of chemically induced mutations in the lacZ gene shortly after exposure provides an effective approach to characterize human-relevant mechanisms of carcinogenesis and propose novel environmental causes of mutation signatures observed in human cancers. Nature Publishing Group UK 2020-08-14 /pmc/articles/PMC7429849/ /pubmed/32796912 http://dx.doi.org/10.1038/s42003-020-01174-y Text en © Crown 2020 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 Beal, Marc A. Meier, Matthew J. LeBlanc, Danielle P. Maurice, Clotilde O’Brien, Jason M. Yauk, Carole L. Marchetti, Francesco Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title | Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title_full | Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title_fullStr | Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title_full_unstemmed | Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title_short | Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures |
title_sort | chemically induced mutations in a mutamouse reporter gene inform mechanisms underlying human cancer mutational signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7429849/ https://www.ncbi.nlm.nih.gov/pubmed/32796912 http://dx.doi.org/10.1038/s42003-020-01174-y |
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