ALKBH5 Modulates Hematopoietic Stem and Progenitor Cell Energy Metabolism Through M 6a Modification-Mediated RNA Stability

We thank Rebecca Cardone and Xiaojian Zhao at the Yale Islet, Oxygen consumption, Mass Isotopomer flux Core (IOMIC) for their help with the Seahorse assay. We thank staff of the CCMI Electron Microscopy Core Facility of Yale School of Medicine for their help with the EM analysis. We thank Diane Trotta at the Yale Flow Core Facility for her help with the flow sorting. The Yale flow cytometry facility is supported in part by an NCI Cancer Center Support Grant (NIH P30 CA016359). The BD Symphony flow cytometer was funded by shared instrument grant (NIH S10 OD026996). BioRender was used to design the graphical abstract. This study was supported by the Animal Modeling Core of the YCCEH (NIDDK U54DK106857), in part by NIH/NIDDK R01DK102792 and R01DK124788 (to S.H.); the Frederick A. DeLuca Foundation (to S.H.); the Edward P. Evans Foundation (to S.H.); NIGMS R01GM137117 (to M.D.S.); in part by the Bill and Melinda Gates Foundation (to R.A.F.); and the Howard Hughes Medical Institute (to R.A.F.). Y.G. was supported by the American Society of Hematology Scholar Award, the National Natural Science Foundation of China (grant no. 82200119), and the Fundamental Research