| Literature DB >> 34433962 |
Luiza Moore1,2, Alex Cagan1, Tim H H Coorens1, Matthew D C Neville1, Rashesh Sanghvi1, Mathijs A Sanders1,3, Thomas R W Oliver1,2, Daniel Leongamornlert1, Peter Ellis1,4, Ayesha Noorani1, Thomas J Mitchell1,5, Timothy M Butler1, Yvette Hooks1, Anne Y Warren2, Mette Jorgensen6, Kevin J Dawson1, Andrew Menzies1, Laura O'Neill1, Calli Latimer1, Mabel Teng1, Ruben van Boxtel7, Christine A Iacobuzio-Donahue8,9, Inigo Martincorena1, Rakesh Heer10,11, Peter J Campbell1, Rebecca C Fitzgerald12, Michael R Stratton13, Raheleh Rahbari14.
Abstract
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.Entities:
Mesh:
Year: 2021 PMID: 34433962 DOI: 10.1038/s41586-021-03822-7
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 69.504