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The mutational landscape of human somatic and germline cells.
Moore, Luiza; Cagan, Alex; Coorens, Tim H H; Neville, Matthew D C; Sanghvi, Rashesh; Sanders, Mathijs A; Oliver, Thomas R W; Leongamornlert, Daniel; Ellis, Peter; Noorani, Ayesha; Mitchell, Thomas J; Butler, Timothy M; Hooks, Yvette; Warren, Anne Y; Jorgensen, Mette; Dawson, Kevin J; Menzies, Andrew; O'Neill, Laura; Latimer, Calli; Teng, Mabel; van Boxtel, Ruben; Iacobuzio-Donahue, Christine A; Martincorena, Inigo; Heer, Rakesh; Campbell, Peter J; Fitzgerald, Rebecca C; Stratton, Michael R; Rahbari, Raheleh.
Afiliação
  • Moore L; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Cagan A; Department of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Coorens THH; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Neville MDC; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Sanghvi R; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Sanders MA; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Oliver TRW; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Leongamornlert D; Department of Hematology, Erasmus University Medical Center, Rotterdam, Netherlands.
  • Ellis P; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Noorani A; Department of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Mitchell TJ; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Butler TM; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Hooks Y; Inivata, Cambridge, UK.
  • Warren AY; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Jorgensen M; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Dawson KJ; Department of Surgery, University of Cambridge, Cambridge, UK.
  • Menzies A; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • O'Neill L; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Latimer C; Department of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Teng M; Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • van Boxtel R; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Iacobuzio-Donahue CA; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Martincorena I; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Heer R; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Campbell PJ; Cancer, Ageing and Somatic Mutation (CASM), Wellcome Sanger Institute, Hinxton, UK.
  • Fitzgerald RC; Princess Máxima Center for Pediatric Oncology and Oncode Institute, Utrecht, Netherlands.
  • Stratton MR; Department of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Rahbari R; Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Nature ; 597(7876): 381-386, 2021 09.
Article em En | MEDLINE | ID: mdl-34433962
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Especificidade de Órgãos / Mutação em Linhagem Germinativa / Taxa de Mutação / Células Germinativas Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Especificidade de Órgãos / Mutação em Linhagem Germinativa / Taxa de Mutação / Células Germinativas Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article