bioRxivCell Biology
Polycomb contraction differentially regulates terminal human hematopoietic differentiation programs
A. Lorzadeh, C. Hammond, D. Knapp, Q. Cao, F. Wang, A. Heravi-Moussavi, M. Wong, M. Bilenky, M. Moksa, Z. Sharafianardakani, P. Lavoie, C. Eaves, M. Hirst
Abstract
Lifelong production of the many types of mature blood cells from less differentiated progenitors is a hierarchically ordered process that spans multiple cell divisions. The nature and timing of the molecular events required to integrate the environmental signals, transcription factor activity, epigenetic modifications, and changes in gene expression involved are thus complex and still poorly understood. We now show that the more primitive types of human cells in this system display a unique repressive H3K27me3 signature that is retained by mature lymphoid cells but is lost in terminally differentiated monocytes and erythroblasts. Additional intervention data implicate that control of this chromatin state change is a requisite part of the process, whereby normal human hematopoietic progenitor cells make lymphoid and myeloid fate decisions.
- organism: human
- assay: ChIP-seq
- research focus: chromatin & epigenetic regulation
- approach: experimental assay
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