Title | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. |
Publication Type | Journal Article |
Year of Publication | 2023 |
Authors | Weinstock, JS, Laurie, CA, Broome, JG, Taylor, KD, Guo, X, Shuldiner, AR, O'Connell, JR, Lewis, JP, Boerwinkle, E, Barnes, KC, Chami, N, Kenny, EE, Loos, RJF, Fornage, M, Redline, S, Cade, BE, Gilliland, FD, Chen, Z, W Gauderman, J, Kumar, R, Grammer, L, Schleimer, RP, Psaty, BM, Bis, JC, Brody, JA, Silverman, EK, Yun, JH, Qiao, D, Weiss, ST, Lasky-Su, J, DeMeo, DL, Palmer, ND, Freedman, BI, Bowden, DW, Cho, MH, Vasan, RS, Johnson, AD, Yanek, LR, Becker, LC, Kardia, S, He, J, Kaplan, R, Heckbert, SR, Smith, NL, Wiggins, KL, Arnett, DK, Irvin, MR, Tiwari, H, Correa, A, Raffield, LM, Gao, Y, de Andrade, M, Rotter, JI, Rich, SS, Manichaikul, AW, Konkle, BA, Johnsen, JM, Wheeler, MM, Custer, BS, Duggirala, R, Curran, JE, Blangero, J, Gui, H, Xiao, S, L Williams, K, Meyers, DA, Li, X, Ortega, V, McGarvey, S, C Gu, C, Chen, Y-DIda, Lee, W-J, M Shoemaker, B, Darbar, D, Roden, D, Albert, C, Kooperberg, C, Desai, P, Blackwell, TW, Abecasis, GR, Smith, AV, Kang, HM, Mathias, R, Natarajan, P, Jaiswal, S, Reiner, AP, Bick, AG |
Corporate Authors | NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium |
Journal | Sci Adv |
Volume | 9 |
Issue | 17 |
Pagination | eabm4945 |
Date Published | 2023 Apr 28 |
ISSN | 2375-2548 |
Keywords | Germ-Line Mutation, Hematopoiesis, Humans, Middle Aged, Mutation, Mutation, Missense, Phenotype |
Abstract | Nononcogenic somatic mutations are thought to be uncommon and inconsequential. To test this, we analyzed 43,693 National Heart, Lung and Blood Institute Trans-Omics for Precision Medicine blood whole genomes from 37 cohorts and identified 7131 non-missense somatic mutations that are recurrently mutated in at least 50 individuals. These recurrent non-missense somatic mutations (RNMSMs) are not clearly explained by other clonal phenomena such as clonal hematopoiesis. RNMSM prevalence increased with age, with an average 50-year-old having 27 RNMSMs. Inherited germline variation associated with RNMSM acquisition. These variants were found in genes involved in adaptive immune function, proinflammatory cytokine production, and lymphoid lineage commitment. In addition, the presence of eight specific RNMSMs associated with blood cell traits at effect sizes comparable to Mendelian genetic mutations. Overall, we found that somatic mutations in blood are an unexpectedly common phenomenon with ancestry-specific determinants and human health consequences. |
DOI | 10.1126/sciadv.abm4945 |
Alternate Journal | Sci Adv |
PubMed ID | 37126548 |
PubMed Central ID | PMC10132750 |
Grant List | R01 HL113323 / HL / NHLBI NIH HHS / United States R01 HL153805 / HL / NHLBI NIH HHS / United States DP2 HL157540 / HL / NHLBI NIH HHS / United States P01 HL132825 / HL / NHLBI NIH HHS / United States K08 HL146972 / HL / NHLBI NIH HHS / United States P01 CA196569 / CA / NCI NIH HHS / United States |
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Similar Publications
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels. Blood. 2024;143(18):1845-1855. | .
Identification of potent pan-ephrin receptor kinase inhibitors using DNA-encoded chemistry technology. Proc Natl Acad Sci U S A. 2024;121(19):e2322934121. | .
Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension. JCI Insight. 2024;9(9). | .