“…Although mtDNA mutations are recognized to accumulate with age (7,19) and mutations within the D-loop are not believed to be under strong selection pressure (18), persistence of mutations has not been tested adequately. While chromosomal translocations are a stable biomarker of radiation exposure of hematopoietic stem cells (34), the kinetics of mitochondrial replication is radically different from that of the nuclear DNA (1), and the long-term persistence of mtDNA muta- C1 100 A16235G, C16261T, C16291T, C16292T No C16021G, G16034A, C16057T, C16107T, T16292C*, G16329&T16330 del §, G16336 del, C16355T C2 96 C16069T, T16126C, G16145A, T16231C, C16261T A16302G (11) G16039A, G16047T, A16212T, C16188T, T16189C, C16348T C3 Exp7 97 G16129A, C16223T, G16391A No G16039 del, C16111T †, T16124C, G16125A, C16256T † Exp8 97 C16069T, T16126C No G16129A †, C16176T, A16258T, C16287T, G16346A † Exp9 96 T16093C, C16192T, A16207G, C16256T, C16270T, C16291T, T16324C, A16399G C16093T ( tions after historical exposure to genotoxic agents is unknown.…”