Identification of DNA methylation changes at cis-regulatory elements during early steps of HSC differentiation using tagmentation-based whole genome bisulfite sequencing
Epigenetic alterations during cellular differentiation are a key molecular mechanism which both instructs and reinforces the process of lineage commitment. Within the haematopoietic system, progressive changes in the DNA methylome of haematopoietic stem cells (HSCs) are essential for the effective p...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
10 December 2014
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| In: |
Cell cycle
Year: 2014, Volume: 13, Issue: 22, Pages: 3476-3487 |
| ISSN: | 1551-4005 |
| DOI: | 10.4161/15384101.2014.973334 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.4161/15384101.2014.973334
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| Author Notes: | Daniel B. Lipka, Qi Wang, Nina Cabezas-Wallscheid, Daniel Klimmeck, Dieter Weichenhan, Carl Herrmann, Amelie Lier, David Brocks, Lisa von Paleske, Simon Renders, Peer Wünsche, Petra Zeisberger, Lei Gu, Simon Haas, Marieke Ag Essers, Benedikt Brors, Roland Eils, Andreas Trumpp, Michael D. Milsom, and Christoph Plass |
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| 520 | |a Epigenetic alterations during cellular differentiation are a key molecular mechanism which both instructs and reinforces the process of lineage commitment. Within the haematopoietic system, progressive changes in the DNA methylome of haematopoietic stem cells (HSCs) are essential for the effective production of mature blood cells. Inhibition or loss of function of the cellular DNA methylation machinery has been shown to lead to a severe perturbation in blood production and is also an important driver of malignant transformation. HSCs constitute a very rare cell population in the bone marrow, capable of life-long self-renewal and multi-lineage differentiation. The low abundance of HSCs has been a major technological barrier to the global analysis of the CpG methylation status within both HSCs and their immediate progeny, the multipotent progenitors (MPPs). Within this Extra View article, we review the current understanding of how the DNA methylome regulates normal and malignant hematopoiesis. We also discuss the current methodologies that are available for interrogating the DNA methylation status of HSCs and MPPs and describe a new data set that was generated using tagmentation-based whole genome bisulfite sequencing (TWGBS) in order to comprehensively map methylated cytosines using the limited amount of genomic DNA that can be harvested from rare cell populations. Extended analysis of this data set clearly demonstrates the added value of genome-wide sequencing of methylated cytosines and identifies novel important cis-acting regulatory regions that are dynamically remodeled during the first steps of haematopoietic differentiation. | ||
| 650 | 4 | |a Cell Differentiation | |
| 650 | 4 | |a differentiation | |
| 650 | 4 | |a DNA methylation | |
| 650 | 4 | |a DNA Methylation | |
| 650 | 4 | |a Epigenesis, Genetic | |
| 650 | 4 | |a epigenetics | |
| 650 | 4 | |a Genome | |
| 650 | 4 | |a haematopoietic stem cells | |
| 650 | 4 | |a Hematopoietic Stem Cells | |
| 650 | 4 | |a High-Throughput Nucleotide Sequencing | |
| 650 | 4 | |a Humans | |
| 650 | 4 | |a progenitor cells | |
| 650 | 4 | |a Regulatory Sequences, Nucleic Acid | |
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