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The mutational landscape of human somatic and germline cells.

Luiza MooreAlex T J CaganTim H H CoorensMatthew D C NevilleRashesh SanghviMathijs A SandersThomas Richard William OliverDaniel A LeongamornlertPeter EllisAyesha NooraniThomas J MitchellTimothy M ButlerYvette HooksAnne Y WarrenMette JorgensenKevin J DawsonAndrew MenziesLaura O'NeillCalli LatimerMabel TengRuben van BoxtelChristine A Iacobuzio-DonahueIñigo MartincorenaRakesh HeerPeter J CampbellRebecca C FitzgeraldMichael R StrattonRaheleh Rahbari
Published in: Nature (2021)
Over the course of an individual's lifetime, normal human cells accumulate mutations1. Here we compare the mutational landscape in 29 cell types from the soma and germline using multiple samples from the same individuals. Two ubiquitous mutational signatures, SBS1 and SBS5/40, accounted for the majority of acquired mutations in most cell types, but their absolute and relative contributions varied substantially. SBS18, which potentially reflects oxidative damage2, and several additional signatures attributed to exogenous and endogenous exposures contributed mutations to subsets of cell types. The rate of mutation was lowest in spermatogonia, the stem cells from which sperm are generated and from which most genetic variation in the human population is thought to originate. This was due to low rates of ubiquitous mutational processes and may be partially attributable to a low rate of cell division in basal spermatogonia. These results highlight similarities and differences in the maintenance of the germline and soma.
Keyphrases
  • single cell
  • endothelial cells
  • cell therapy
  • dna repair
  • gene expression
  • cell death
  • oxidative stress
  • cell proliferation
  • peripheral blood
  • dna methylation
  • induced pluripotent stem cells