The RUNX family of transcription factors plays important roles in tissue-specific gene expression. Many of their functions depend on specific post-translational modifications (PTMs), and in this review, we describe how PTMs govern RUNX DNA binding, transcriptional activity, protein stability, cellular localization, and protein-protein interactions. We also report how these processes can be disrupted in disease settings. Finally, we describe how alterations of RUNX1, or the enzymes that catalyze its post-translational modifications, contribute to hematopoietic malignancies.
Keywords: Acetylation; Acute Myeloid Leukemia; CBFβ; Cleidocranial Dysplasia; FPD/AML; Methylation; Phosphorylation; Post-Translational Modifications; RUNX1; RUNX2; RUNX3; Transcriptional Activation; Transcriptional Repression; Ubiquitylation.