RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues

Keren Yizhak(Broad Institute), François Aguet(Broad Institute), Jaegil Kim(Broad Institute), Julian M. Hess(Broad Institute), Kirsten Kübler(Broad Institute), Jonna Grimsby(Broad Institute), Ruslana Frazer(Broad Institute), Hailei Zhang(Broad Institute), Nicholas J. Haradhvala(Broad Institute), Daniel Rosebrock(Broad Institute), Dimitri Livitz(Broad Institute), Xiao Li(Broad Institute), Eila Arich-Landkof(Broad Institute), Noam Shoresh(Broad Institute), Chip Stewart(Broad Institute), Ayellet V. Segrè(Broad Institute), Philip A. Branton(Specim (Finland)), Paz Polak(Mount Sinai Hospital), Kristin Ardlie(Broad Institute), Gad Getz(Broad Institute)
Science
June 6, 2019
Cited by 514Open Access
Full Text

Abstract

How somatic mutations accumulate in normal cells is poorly understood. A comprehensive analysis of RNA sequencing data from ~6700 samples across 29 normal tissues revealed multiple somatic variants, demonstrating that macroscopic clones can be found in many normal tissues. We found that sun-exposed skin, esophagus, and lung have a higher mutation burden than other tested tissues, which suggests that environmental factors can promote somatic mosaicism. Mutation burden was associated with both age and tissue-specific cell proliferation rate, highlighting that mutations accumulate over both time and number of cell divisions. Finally, normal tissues were found to harbor mutations in known cancer genes and hotspots. This study provides a broad view of macroscopic clonal expansion in human tissues, thus serving as a foundation for associating clonal expansion with environmental factors, aging, and risk of disease.


Related Papers

No related papers found

Powered by citation graph analysis