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Ribosomal protein control of hematopoietic stem cell transformation through direct, non-canonical regulation of metabolism

GSE302046 Mus musculus Expression profiling by high throughput sequencing 6 samples Submitted 2025/09/30 Platform GPL30172
Summary
We report here that expression of the ribosomal protein, RPL22, is frequently reduced in human myelodysplastic syndrome (MDS) and acute myelogenous leukemia (AML); reduced RPL22 expression is associated with worse outcomes. Mice null for Rpl22 display characteristics of an MDS-like syndrome and develop leukemia at an accelerated rate. Rpl22-deficient mice also display enhanced hematopoietic stem cell (HSC) self-renewal and obstructed differentiation potential, which arises not from reduced protein synthesis but from increased expression of the Rpl22 target, ALOX12, an upstream regulator of fatty acid oxidation (FAO). The increased FAO mediated by Rpl22-deficiency also persists in leukemia cells and promotes their survival. Altogether, these findings reveal that Rpl22 insufficiency enhances the leukemia potential of HSC via non-canonical de-repression of its target, ALOX12, which enhances FAO, a process that may serve as a therapeutic vulnerability of Rpl22 low MDS and AML leukemia cells.
Published in
Ribosomal protein control of hematopoietic stem cell transformation through regulation of metabolism
Harris B, Singh DK, Truong B et al. · Cell reports 2025 · PMID 41389200 · doi:10.1016/j.celrep.2025.116688
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Also filed as BioProject PRJNA1288414 and SRA study SRP599138. Searching any of these in the dataset finder brings you back here.

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