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Heterochromatin and Polycomb as regulators of haematopoiesis

Haematopoiesis is the process by which multipotent haematopoietic stem cells are transformed into each and every type of terminally differentiated blood cell. Epigenetic silencing is critical for this process by regulating the transcription of cell-cycle genes critical for self-renewal and different...

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Autor principal: Keenan, Christine R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106494/
https://www.ncbi.nlm.nih.gov/pubmed/33929498
http://dx.doi.org/10.1042/BST20200737
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author Keenan, Christine R.
author_facet Keenan, Christine R.
author_sort Keenan, Christine R.
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description Haematopoiesis is the process by which multipotent haematopoietic stem cells are transformed into each and every type of terminally differentiated blood cell. Epigenetic silencing is critical for this process by regulating the transcription of cell-cycle genes critical for self-renewal and differentiation, as well as restricting alternative fate genes to allow lineage commitment and appropriate differentiation. There are two distinct forms of transcriptionally repressed chromatin: H3K9me3-marked heterochromatin and H3K27me3/H2AK119ub1-marked Polycomb (often referred to as facultative heterochromatin). This review will discuss the role of these distinct epigenetic silencing mechanisms in regulating normal haematopoiesis, how these contribute to age-related haematopoietic dysfunction, and the rationale for therapeutic targeting of these pathways in the treatment of haematological malignancies.
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spelling pubmed-81064942021-05-18 Heterochromatin and Polycomb as regulators of haematopoiesis Keenan, Christine R. Biochem Soc Trans Review Articles Haematopoiesis is the process by which multipotent haematopoietic stem cells are transformed into each and every type of terminally differentiated blood cell. Epigenetic silencing is critical for this process by regulating the transcription of cell-cycle genes critical for self-renewal and differentiation, as well as restricting alternative fate genes to allow lineage commitment and appropriate differentiation. There are two distinct forms of transcriptionally repressed chromatin: H3K9me3-marked heterochromatin and H3K27me3/H2AK119ub1-marked Polycomb (often referred to as facultative heterochromatin). This review will discuss the role of these distinct epigenetic silencing mechanisms in regulating normal haematopoiesis, how these contribute to age-related haematopoietic dysfunction, and the rationale for therapeutic targeting of these pathways in the treatment of haematological malignancies. Portland Press Ltd. 2021-04-30 2021-04-30 /pmc/articles/PMC8106494/ /pubmed/33929498 http://dx.doi.org/10.1042/BST20200737 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . Open access for this article was enabled by the participation of the Walter and Eliza Hall Institute in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with CAUL.
spellingShingle Review Articles
Keenan, Christine R.
Heterochromatin and Polycomb as regulators of haematopoiesis
title Heterochromatin and Polycomb as regulators of haematopoiesis
title_full Heterochromatin and Polycomb as regulators of haematopoiesis
title_fullStr Heterochromatin and Polycomb as regulators of haematopoiesis
title_full_unstemmed Heterochromatin and Polycomb as regulators of haematopoiesis
title_short Heterochromatin and Polycomb as regulators of haematopoiesis
title_sort heterochromatin and polycomb as regulators of haematopoiesis
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106494/
https://www.ncbi.nlm.nih.gov/pubmed/33929498
http://dx.doi.org/10.1042/BST20200737
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