RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues.
Keren YizhakFrançois AguetJaegil KimJulian M HessKirsten KüblerJonna L GrimsbyRuslana FrazerHailei ZhangNicholas J HaradhvalaDaniel RosebrockDimitri LivitzXiao LiEila Arich-LandkofNoam ShoreshChip StewartAyellet V SegrèPhilip A BrantonPaz PolakKristin G ArdlieGad A GetzPublished in: Science (New York, N.Y.) (2019)
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.
Keyphrases
- gene expression
- copy number
- single cell
- cell proliferation
- endothelial cells
- induced apoptosis
- oxidative stress
- electronic health record
- papillary thyroid
- risk factors
- cell therapy
- artificial intelligence
- young adults
- cell cycle arrest
- endoplasmic reticulum stress
- nucleic acid
- induced pluripotent stem cells
- data analysis