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RUNX1 deficiency cooperates with SRSF2 mutation to induce multilineage hematopoietic defects characteristic of MDS

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Key Points • Coexistence of the Srsf2 P95H mutation and Runx1 deficiency recapitulates the multilineage hematopoietic defects observed in MDS.• RUNX1 deficiency strikingly alters global splicing patterns and synergizes with… Click to show full abstract

Key Points • Coexistence of the Srsf2 P95H mutation and Runx1 deficiency recapitulates the multilineage hematopoietic defects observed in MDS.• RUNX1 deficiency strikingly alters global splicing patterns and synergizes with the Srsf2 P95H mutation to affect DNA damage response genes.

Keywords: runx1 deficiency; multilineage hematopoietic; hematopoietic defects; mds runx1; mutation

Journal Title: Blood Advances
Year Published: 2022

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