| Literature DB >> 31171663 |
Keren Yizhak1, François Aguet1, Jaegil Kim1, Julian M Hess1, Kirsten Kübler1,2,3, Jonna Grimsby1, Ruslana Frazer1, Hailei Zhang1, Nicholas J Haradhvala1,2, Daniel Rosebrock1, Dimitri Livitz1, Xiao Li1, Eila Arich-Landkof1,2, Noam Shoresh1, Chip Stewart1, Ayellet V Segrè1,3,4, Philip A Branton5, Paz Polak6, Kristin G Ardlie1, Gad Getz7,2,3,8.
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.Entities:
Mesh:
Year: 2019 PMID: 31171663 PMCID: PMC7350423 DOI: 10.1126/science.aaw0726
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728