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Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium
We investigated the means and timing by which mutations become fixed in the human colonic epithelium by visualizing somatic clones and mathematical inference. Fixation requires two sequential steps. First, one of approximately seven active stem cells residing within each colonic crypt has to be muta...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989058/ https://www.ncbi.nlm.nih.gov/pubmed/29779891 http://dx.doi.org/10.1016/j.stem.2018.04.020 |
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author | Nicholson, Anna M. Olpe, Cora Hoyle, Alice Thorsen, Ann-Sofie Rus, Teja Colombé, Mathilde Brunton-Sim, Roxanne Kemp, Richard Marks, Kate Quirke, Phil Malhotra, Shalini ten Hoopen, Rogier Ibrahim, Ashraf Lindskog, Cecilia Myers, Meagan B. Parsons, Barbara Tavaré, Simon Wilkinson, Mark Morrissey, Edward Winton, Douglas J. |
author_facet | Nicholson, Anna M. Olpe, Cora Hoyle, Alice Thorsen, Ann-Sofie Rus, Teja Colombé, Mathilde Brunton-Sim, Roxanne Kemp, Richard Marks, Kate Quirke, Phil Malhotra, Shalini ten Hoopen, Rogier Ibrahim, Ashraf Lindskog, Cecilia Myers, Meagan B. Parsons, Barbara Tavaré, Simon Wilkinson, Mark Morrissey, Edward Winton, Douglas J. |
author_sort | Nicholson, Anna M. |
collection | PubMed |
description | We investigated the means and timing by which mutations become fixed in the human colonic epithelium by visualizing somatic clones and mathematical inference. Fixation requires two sequential steps. First, one of approximately seven active stem cells residing within each colonic crypt has to be mutated. Second, the mutated stem cell has to replace neighbors to populate the entire crypt in a process that takes several years. Subsequent clonal expansion due to crypt fission is infrequent for neutral mutations (around 0.7% of all crypts undergo fission in a single year). Pro-oncogenic mutations subvert both stem cell replacement to accelerate fixation and clonal expansion by crypt fission to achieve high mutant allele frequencies with age. The benchmarking of these behaviors allows the advantage associated with different gene-specific mutations to be compared irrespective of the cellular mechanisms by which they are conferred. |
format | Online Article Text |
id | pubmed-5989058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59890582018-06-06 Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium Nicholson, Anna M. Olpe, Cora Hoyle, Alice Thorsen, Ann-Sofie Rus, Teja Colombé, Mathilde Brunton-Sim, Roxanne Kemp, Richard Marks, Kate Quirke, Phil Malhotra, Shalini ten Hoopen, Rogier Ibrahim, Ashraf Lindskog, Cecilia Myers, Meagan B. Parsons, Barbara Tavaré, Simon Wilkinson, Mark Morrissey, Edward Winton, Douglas J. Cell Stem Cell Article We investigated the means and timing by which mutations become fixed in the human colonic epithelium by visualizing somatic clones and mathematical inference. Fixation requires two sequential steps. First, one of approximately seven active stem cells residing within each colonic crypt has to be mutated. Second, the mutated stem cell has to replace neighbors to populate the entire crypt in a process that takes several years. Subsequent clonal expansion due to crypt fission is infrequent for neutral mutations (around 0.7% of all crypts undergo fission in a single year). Pro-oncogenic mutations subvert both stem cell replacement to accelerate fixation and clonal expansion by crypt fission to achieve high mutant allele frequencies with age. The benchmarking of these behaviors allows the advantage associated with different gene-specific mutations to be compared irrespective of the cellular mechanisms by which they are conferred. Cell Press 2018-06-01 /pmc/articles/PMC5989058/ /pubmed/29779891 http://dx.doi.org/10.1016/j.stem.2018.04.020 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nicholson, Anna M. Olpe, Cora Hoyle, Alice Thorsen, Ann-Sofie Rus, Teja Colombé, Mathilde Brunton-Sim, Roxanne Kemp, Richard Marks, Kate Quirke, Phil Malhotra, Shalini ten Hoopen, Rogier Ibrahim, Ashraf Lindskog, Cecilia Myers, Meagan B. Parsons, Barbara Tavaré, Simon Wilkinson, Mark Morrissey, Edward Winton, Douglas J. Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title | Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title_full | Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title_fullStr | Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title_full_unstemmed | Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title_short | Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium |
title_sort | fixation and spread of somatic mutations in adult human colonic epithelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989058/ https://www.ncbi.nlm.nih.gov/pubmed/29779891 http://dx.doi.org/10.1016/j.stem.2018.04.020 |
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