| Literature DB >> 25043003 |
Meritxell Huch1,2, Ruben van Boxtel1, Wouter Karthaus1, Sam Behjati3,4, David C Wedge3, Asif U Tamuri5, Inigo Martincorena3, Mia Petljak3, Ludmil B Alexandrov3, Gunes Gundem3, Patrick S Tarpey3, Sophie Roerink3, Joyce Blokker1, Mark Maddison3, Laura Mudie3, Ben Robinson3, Serena Nik-Zainal3,6, Peter Campbell3, Nick Goldman5, Marc van de Wetering1, Edwin Cuppen1, Hans Clevers1, Michael R Stratton3.
Abstract
The somatic mutations present in the genome of a cell accumulate over the lifetime of a multicellular organism. These mutations can provide insights into the developmental lineage tree, the number of divisions that each cell has undergone and the mutational processes that have been operative. Here we describe whole genomes of clonal lines derived from multiple tissues of healthy mice. Using somatic base substitutions, we reconstructed the early cell divisions of each animal, demonstrating the contributions of embryonic cells to adult tissues. Differences were observed between tissues in the numbers and types of mutations accumulated by each cell, which likely reflect differences in the number of cell divisions they have undergone and varying contributions of different mutational processes. If somatic mutation rates are similar to those in mice, the results indicate that precise insights into development and mutagenesis of normal human cells will be possible.Entities:
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Year: 2014 PMID: 25043003 PMCID: PMC4227286 DOI: 10.1038/nature13448
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962