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A pan-tissue survey of mosaic chromosomal alterations in 948 individuals.

Teng GaoMaria Eleni KastritiViktor LjungströmAndreas HeinzelArthur S TischlerRainer OberbauerPo-Ru LohIgor AdameykoPeter J ParkPeter V Kharchenko
Published in: Nature genetics (2023)
Genetic mutations accumulate in an organism's body throughout its lifetime. While somatic single-nucleotide variants have been well characterized in the human body, the patterns and consequences of large chromosomal alterations in normal tissues remain largely unknown. Here, we present a pan-tissue survey of mosaic chromosomal alterations (mCAs) in 948 healthy individuals from the Genotype-Tissue Expression project, augmenting RNA-based allelic imbalance estimation with haplotype phasing. We found that approximately a quarter of the individuals carry a clonally-expanded mCA in at least one tissue, with incidence strongly correlated with age. The prevalence and genome-wide patterns of mCAs vary considerably across tissue types, suggesting tissue-specific mutagenic exposure and selection pressures. The mCA landscapes in normal adrenal and pituitary glands resemble those in tumors arising from these tissues, whereas the same is not true for the esophagus and skin. Together, our findings show a widespread age-dependent emergence of mCAs across normal human tissues with intricate connections to tumorigenesis.
Keyphrases
  • copy number
  • genome wide
  • endothelial cells
  • gene expression
  • risk factors
  • poor prognosis
  • pluripotent stem cells
  • soft tissue
  • growth hormone