Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing

• Published in: Proceedings of the National Academy of Sciences - PNAS 2016-08, Vol.113 (35), p.9846-9851
• Main Authors: Hoang, Margaret L., Kinde, Isaac, Tomasetti, Cristian, McMahon, K. Wyatt, Rosenquist, Thomas A., Grollman, Arthur P., Kinzler, Kenneth W., Vogelstein, Bert, Papadopoulos, Nickolas
• Format: Article
• Language: English
• Subjects: Biological Sciences; Cancer; Genomes; Mitochondria; Mutation; Tissues
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1607794113

We present the bottleneck sequencing system (BotSeqS), a next-generation sequencing method that simultaneously quantifies rare somatic point mutations across the mitochondrial and nuclear genomes. BotSeqS combines molecular barcoding with a simple dilution step immediately before library amplification. We use BotSeqS to show age- and tissue-dependent accumulations of rare mutations and demonstrate that somatic mutational burden in normal human tissues can vary by several orders of magnitude, depending on biologic and environmental factors. We further show major differences between the mutational patterns of the mitochondrial and nuclear genomes in normal tissues. Lastly, the mutation spectra of normal tissues were different from each other, but similar to those of the cancers that arose in them. This technology can provide insights into the number and nature of genetic alterations in normal tissues and can be used to address a variety of fundamental questions about the genomes of diseased tissues.