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| Home > Publications database > Metabolite-induced DNA damage drives stochastic stem cell loss and clonal hematopoiesis. |
| Home > Publications database > Metabolite-induced DNA damage drives stochastic stem cell loss and clonal hematopoiesis. |
| Journal Article | DKFZ-2026-00665 |
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2026
Elsevier
Amsterdam [u.a.]
Abstract: DNA damage and mutations in hematopoietic stem cells (HSCs) enable clonal hematopoiesis (CH). Such damage occurs across a lifetime, but its origins remain unknown. Here, we demonstrate that endogenous formaldehyde causes HSC attrition and subsequently CH. We generated conditional mouse models lacking formaldehyde detoxification and Fanconi anemia (FA) DNA repair in blood. Formaldehyde protection was crucial for embryonic HSC emergence and throughout life. Despite severe deficiencies in HSCs, these mice produced blood for many months. To determine what enables this, we employed an unbiased method for detecting clones, which exploits somatic variant data. This revealed initial polyclonal hematopoiesis that diminishes to monoclonal hematopoiesis, devoid of known genetic selection. Furthermore, in FA children, we find the same transition to monoclonal hematopoiesis. Therefore, DNA damage-induced attrition down to the last functional cell can be a driving force for CH, representing an alternative route to CH other than purely by fitness-enhancing selection.
Keyword(s): Fanconi anemia ; HSC attrition ; bone marrow failure ; clonal hematopoiesis ; endogenous DNA damage ; formaldehyde ; neutral drift ; somatic evolution ; stem cell aging
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