Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate

Rodrigues CP, Herman JS, Herquel B, Valsecchi CIKL, Stehle T, Gruen D, Akhtar A (2020)


Publication Type: Journal article

Publication year: 2020

Journal

Book Volume: 6

Pages Range: eaaz4815-

Journal Issue: 21

DOI: 10.1126/sciadv.aaz4815

Abstract

Self-renewal and differentiation of hematopoietic stem cells (HSCs) are orchestrated by the combinatorial action of transcription factors and epigenetic regulators. Here, we have explored the mechanism by which histone H4 lysine 16 acetyltransferase MOF regulates erythropoiesis. Single-cell RNA sequencing and chromatin immunoprecipitation sequencing uncovered that MOF influences erythroid trajectory by dynamic recruitment to chromatin and its haploinsufficiency causes accumulation of a transient HSC population. A regulatory network consisting of MOF, RUNX1, and GFI1B is critical for erythroid fate commitment. GFI1B acts as a Mof activator which is necessary and sufficient for cell type-specific induction of Mof expression. Plasticity of Mof-depleted HSCs can be rescued by expression of a downstream effector, Gata1, or by rebalancing acetylation via a histone deacetylase inhibitor. Accurate timing and dosage of Mof expression act as a rheostat for the feedforward transcription factor network that safeguards progression along the erythroid fate.

Involved external institutions

How to cite

APA:

Rodrigues, C.P., Herman, J.S., Herquel, B., Valsecchi, C.I.K.L., Stehle, T., Gruen, D., & Akhtar, A. (2020). Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate. Science Advances, 6(21), eaaz4815-. https://doi.org/10.1126/sciadv.aaz4815

MLA:

Rodrigues, Cecilia Pessoa, et al. "Temporal expression of MOF acetyltransferase primes transcription factor networks for erythroid fate." Science Advances 6.21 (2020): eaaz4815-.

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