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The landscape of somatic mutations in lymphoblastoid cell lines
Somatic mutations have important biological ramifications while exerting substantial rate, type, and genomic location heterogeneity. Yet, their sporadic occurrence makes them difficult to study at scale and across individuals. Lymphoblastoid cell lines (LCLs), a model system for human population and...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300552/ https://www.ncbi.nlm.nih.gov/pubmed/37388907 http://dx.doi.org/10.1016/j.xgen.2023.100305 |
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author | Caballero, Madison Koren, Amnon |
author_facet | Caballero, Madison Koren, Amnon |
author_sort | Caballero, Madison |
collection | PubMed |
description | Somatic mutations have important biological ramifications while exerting substantial rate, type, and genomic location heterogeneity. Yet, their sporadic occurrence makes them difficult to study at scale and across individuals. Lymphoblastoid cell lines (LCLs), a model system for human population and functional genomics, harbor large numbers of somatic mutations and have been extensively genotyped. By comparing 1,662 LCLs, we report that the mutational landscape of the genome varies across individuals in terms of the number of mutations, their genomic locations, and their spectra; this variation may itself be modulated by somatic trans-acting mutations. Mutations attributed to the translesion DNA polymerase η follow two different modes of formation, with one mode accounting for the hypermutability of the inactive X chromosome. Nonetheless, the distribution of mutations along the inactive X chromosome appears to follow an epigenetic memory of the active form. |
format | Online Article Text |
id | pubmed-10300552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103005522023-06-29 The landscape of somatic mutations in lymphoblastoid cell lines Caballero, Madison Koren, Amnon Cell Genom Article Somatic mutations have important biological ramifications while exerting substantial rate, type, and genomic location heterogeneity. Yet, their sporadic occurrence makes them difficult to study at scale and across individuals. Lymphoblastoid cell lines (LCLs), a model system for human population and functional genomics, harbor large numbers of somatic mutations and have been extensively genotyped. By comparing 1,662 LCLs, we report that the mutational landscape of the genome varies across individuals in terms of the number of mutations, their genomic locations, and their spectra; this variation may itself be modulated by somatic trans-acting mutations. Mutations attributed to the translesion DNA polymerase η follow two different modes of formation, with one mode accounting for the hypermutability of the inactive X chromosome. Nonetheless, the distribution of mutations along the inactive X chromosome appears to follow an epigenetic memory of the active form. Elsevier 2023-05-02 /pmc/articles/PMC10300552/ /pubmed/37388907 http://dx.doi.org/10.1016/j.xgen.2023.100305 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Caballero, Madison Koren, Amnon The landscape of somatic mutations in lymphoblastoid cell lines |
title | The landscape of somatic mutations in lymphoblastoid cell lines |
title_full | The landscape of somatic mutations in lymphoblastoid cell lines |
title_fullStr | The landscape of somatic mutations in lymphoblastoid cell lines |
title_full_unstemmed | The landscape of somatic mutations in lymphoblastoid cell lines |
title_short | The landscape of somatic mutations in lymphoblastoid cell lines |
title_sort | landscape of somatic mutations in lymphoblastoid cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300552/ https://www.ncbi.nlm.nih.gov/pubmed/37388907 http://dx.doi.org/10.1016/j.xgen.2023.100305 |
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