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A body map of somatic mutagenesis in morphologically normal human tissues
A body map of somatic mutagenesis in morphologically normal human tissues
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A body map of somatic mutagenesis in morphologically normal human tissues
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A body map of somatic mutagenesis in morphologically normal human tissues
A body map of somatic mutagenesis in morphologically normal human tissues

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A body map of somatic mutagenesis in morphologically normal human tissues
A body map of somatic mutagenesis in morphologically normal human tissues
Journal Article

A body map of somatic mutagenesis in morphologically normal human tissues

2021
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Overview
Somatic mutations that accumulate in normal tissues are associated with ageing and disease 1 , 2 . Here we performed a comprehensive genomic analysis of 1,737 morphologically normal tissue biopsies of 9 organs from 5 donors. We found that somatic mutation accumulations and clonal expansions were widespread, although to variable extents, in morphologically normal human tissues. Somatic copy number alterations were rarely detected, except for in tissues from the oesophagus and cardia. Endogenous mutational processes with the SBS1 and SBS5 mutational signatures are ubiquitous among normal tissues, although they exhibit different relative activities. Exogenous mutational processes operate in multiple tissues from the same donor. We reconstructed the spatial somatic clonal architecture with sub-millimetre resolution. In the oesophagus and cardia, macroscopic somatic clones that expanded to hundreds of micrometres were frequently seen, whereas in tissues such as the colon, rectum and duodenum, somatic clones were microscopic in size and evolved independently, possibly restricted by local tissue microstructures. Our study depicts a body map of somatic mutations and clonal expansions from the same individual. Laser-capture microdissection and mini-bulk exome sequencing are combined to analyse somatic mutations in morphologically normal tissues from nine organs from five donors, revealing variation in mutation burdens, mutational signatures and clonal expansions.