4.7 Article

Fixation and Spread of Somatic Mutations in Adult Human Colonic Epithelium

Journal

CELL STEM CELL
Volume 22, Issue 6, Pages 909-+

Publisher

CELL PRESS
DOI: 10.1016/j.stem.2018.04.020

Keywords

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Funding

  1. Norwich Research Park BioRepository (Human Tissue Authority) [11208 08/H0304/85+5, 11208]
  2. BBSRC
  3. Norfolk and Norwich University Hospitals NHS Foundation Trust
  4. University of East Anglia
  5. Addenbrooke's Human Research Tissue Bank
  6. NIHR Cambridge Biomedical Research Centre
  7. Wellcome Trust [103805]
  8. Cancer Research UK
  9. Wellcome four-year Ph.D. studentship
  10. MRC Computational Biology Fellowship [MC_UU_12025]

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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.

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