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APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types
BACKGROUND: The APOBEC3 (apolipoprotein B mRNA editing enzyme catalytic polypeptide 3) family of cytidine deaminases is responsible for two mutational signatures (SBS2 and SBS13) found in cancer genomes. APOBEC3 enzymes are activated in response to viral infection, and have been associated with incr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124393/ https://www.ncbi.nlm.nih.gov/pubmed/35597990 http://dx.doi.org/10.1186/s12915-022-01316-0 |
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author | Jakobsdottir, G. Maria Brewer, Daniel S Cooper, Colin Green, Catherine Wedge, David C |
author_facet | Jakobsdottir, G. Maria Brewer, Daniel S Cooper, Colin Green, Catherine Wedge, David C |
author_sort | Jakobsdottir, G. Maria |
collection | PubMed |
description | BACKGROUND: The APOBEC3 (apolipoprotein B mRNA editing enzyme catalytic polypeptide 3) family of cytidine deaminases is responsible for two mutational signatures (SBS2 and SBS13) found in cancer genomes. APOBEC3 enzymes are activated in response to viral infection, and have been associated with increased mutation burden and TP53 mutation. In addition to this, it has been suggested that APOBEC3 activity may be responsible for mutations that do not fall into the classical APOBEC3 signatures (SBS2 and SBS13), through generation of double strand breaks.Previous work has mainly focused on the effects of APOBEC3 within individual tumour types using exome sequencing data. Here, we use whole genome sequencing data from 2451 primary tumours from 39 different tumour types in the Pan-Cancer Analysis of Whole Genomes (PCAWG) data set to investigate the relationship between APOBEC3 and genomic instability (GI). RESULTS AND CONCLUSIONS: We found that the number of classical APOBEC3 signature mutations correlates with increased mutation burden across different tumour types. In addition, the number of APOBEC3 mutations is a significant predictor for six different measures of GI. Two GI measures (INDELs attributed to INDEL signatures ID6 and ID8) strongly suggest the occurrence and error prone repair of double strand breaks, and the relationship between APOBEC3 mutations and GI remains when SNVs attributed to kataegis are excluded.We provide evidence that supports a model of cancer genome evolution in which APOBEC3 acts as a causative factor in the development of diverse and widespread genomic instability through the generation of double strand breaks. This has important implications for treatment approaches for cancers that carry APOBEC3 mutations, and challenges the view that APOBECs only act opportunistically at sites of single stranded DNA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12915-022-01316-0). |
format | Online Article Text |
id | pubmed-9124393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91243932022-05-23 APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types Jakobsdottir, G. Maria Brewer, Daniel S Cooper, Colin Green, Catherine Wedge, David C BMC Biol Research Article BACKGROUND: The APOBEC3 (apolipoprotein B mRNA editing enzyme catalytic polypeptide 3) family of cytidine deaminases is responsible for two mutational signatures (SBS2 and SBS13) found in cancer genomes. APOBEC3 enzymes are activated in response to viral infection, and have been associated with increased mutation burden and TP53 mutation. In addition to this, it has been suggested that APOBEC3 activity may be responsible for mutations that do not fall into the classical APOBEC3 signatures (SBS2 and SBS13), through generation of double strand breaks.Previous work has mainly focused on the effects of APOBEC3 within individual tumour types using exome sequencing data. Here, we use whole genome sequencing data from 2451 primary tumours from 39 different tumour types in the Pan-Cancer Analysis of Whole Genomes (PCAWG) data set to investigate the relationship between APOBEC3 and genomic instability (GI). RESULTS AND CONCLUSIONS: We found that the number of classical APOBEC3 signature mutations correlates with increased mutation burden across different tumour types. In addition, the number of APOBEC3 mutations is a significant predictor for six different measures of GI. Two GI measures (INDELs attributed to INDEL signatures ID6 and ID8) strongly suggest the occurrence and error prone repair of double strand breaks, and the relationship between APOBEC3 mutations and GI remains when SNVs attributed to kataegis are excluded.We provide evidence that supports a model of cancer genome evolution in which APOBEC3 acts as a causative factor in the development of diverse and widespread genomic instability through the generation of double strand breaks. This has important implications for treatment approaches for cancers that carry APOBEC3 mutations, and challenges the view that APOBECs only act opportunistically at sites of single stranded DNA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s12915-022-01316-0). BioMed Central 2022-05-21 /pmc/articles/PMC9124393/ /pubmed/35597990 http://dx.doi.org/10.1186/s12915-022-01316-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Jakobsdottir, G. Maria Brewer, Daniel S Cooper, Colin Green, Catherine Wedge, David C APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title | APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title_full | APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title_fullStr | APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title_full_unstemmed | APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title_short | APOBEC3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
title_sort | apobec3 mutational signatures are associated with extensive and diverse genomic instability across multiple tumour types |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124393/ https://www.ncbi.nlm.nih.gov/pubmed/35597990 http://dx.doi.org/10.1186/s12915-022-01316-0 |
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