bioRxivCancer Biology
A heterozygous CEBPA mutation disrupting the bZIP domain causes MDS disease progression
R. Almaghrabi, Y. Alyayhawi, P. Keane, C. R. J. Ward, R. Bayley, C. Sargas, P. Menendez, G. J. Murphy, T. Sobahy, M. A. Baghdadi, A. F. Flemban, S. Kabrah, I. Akerman, M. Raghavan, E. Barragan, C. Bonifer, P. Garcia
Abstract
Myelodysplastic syndrome disease (MDS) has a variable risk for progression to AML. Mutations in CEBPA are associated with a high risk of disease progression, but whether this mutation is causative for AML development is unclear. To answer this question, we generated patient-derived, MDS-specific iPSCs recapitulating the patient disease phenotype upon differentiation to blood, with hematopoietic progenitor cells showing erythroid and myeloid-dysplasia. Introduction of a frameshift mutation affecting the C/EBP bZIP domain led to disease progression, with a reduction in clonogenic potential, block in granulocyte development and increased self-renewal capacity of erythroid progenitors. ATAC-seq revealed that the acquisition of this mutation reshaped the chromatin landscape at distal cis-regulatory regions, promoting changes in clonal composition as observed by single cell RNAseq. Our work identifies mutant CEBPA as causative for MDS disease progression, providing a new isogenic MDS experimental model for drug screening to improve diagnostic and therapeutic strategies. HighlightsO_LIDevelopment of isogenic iPSC model of clonal evolution of MDS C_LIO_LIMonoallelic disruption of CEBPA bZIP domain is causative for MDS disease progression C_LIO_LIMonoallelic disruption of CEBPA bZIP reshapes chromatin landscape C_LIO_LIPatient derived iPSCs recapitulate drug responsiveness C_LI
- organism: human
- assay: ATAC-seq
- assay: scRNA-seq
- research focus: cell type annotation
- research focus: chromatin & epigenetic regulation
- research focus: differential expression
- research focus: drug response / drug discovery
- approach: experimental assay
- approach: wet-lab / biochemical assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Cholesterol Biosynthesis is a Targetable Vulnerability of CEBPA-mutant Acute Myeloid Leukemia
Sofie Ulfbeck Schovsbo, Yang Liu, … Bo Torben Porse·bioRxiv·Feb 20, 2026
- TET2 lesions enhance the aggressiveness of CEBPA-mutant AML by rebalancing GATA2 expression
E. Heyes, A. S. Wilhelmson, … B. T. Porse·bioRxiv·Mar 28, 2023
- PTPRJ Drives Clonal Selection in CEBPA mutated AML
Alexandra Lubin, Catherine Hockings, … Elspeth M. Payne·bioRxiv·Jul 8, 2026
- A C/ebpα isoform-specific differentiation program in primary myelocytes
M.-P. Garcia-Cuellar, S. Akan, R. K. Slany·bioRxiv·May 16, 2023
- IL-1B-mediated inflammatory signaling drives ineffective erythropoiesis in early-stage myelodysplastic syndromes
V. Adema, I. Ganan-Gomez, … S. Colla·bioRxiv·Sep 28, 2023
- Human CEBPA-N AML exhibits enhanced engraftment and a C/EBPα-p30-driven leukemic stem cell program
Philomina Sona Peramangalam, Mayuresh Vishwas Konde, … John Anto Pulikkan·bioRxiv·Aug 4, 2026