The origins and functional effects of postzygotic mutations throughout the human life span

Author:

Rockweiler Nicole B.1ORCID,Ramu Avinash1ORCID,Nagirnaja Liina2ORCID,Wong Wing H.3ORCID,Noordam Michiel J.1,Drubin Casey W.1ORCID,Huang Ni1ORCID,Miller Brian2ORCID,Todres Ellen Z.4ORCID,Vigh-Conrad Katinka A.2ORCID,Zito Antonino5ORCID,Small Kerrin S.5ORCID,Ardlie Kristin G.4ORCID,Cohen Barak A.1ORCID,Conrad Donald F.126ORCID

Affiliation:

1. Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.

2. Division of Genetics, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.

3. Department of Pediatrics, Division of Hematology and Oncology, Washington University School of Medicine, St. Louis, MO 63110, USA.

4. Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

5. Department of Twin Research and Genetic Epidemiology, King’s College London, London SE1 7EH, UK.

6. Center for Embryonic Cell and Gene Therapy, Oregon Health & Science University, Portland, OR 97239, USA.

Abstract

Postzygotic mutations (PZMs) begin to accrue in the human genome immediately after fertilization, but how and when PZMs affect development and lifetime health remain unclear. To study the origins and functional consequences of PZMs, we generated a multitissue atlas of PZMs spanning 54 tissue and cell types from 948 donors. Nearly half the variation in mutation burden among tissue samples can be explained by measured technical and biological effects, and 9% can be attributed to donor-specific effects. Through phylogenetic reconstruction of PZMs, we found that their type and predicted functional impact vary during prenatal development, across tissues, and through the germ cell life cycle. Thus, methods for interpreting effects across the body and the life span are needed to fully understand the consequences of genetic variants.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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