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Pre-mitotic genome re-organisation bookends the B cell differentiation process

During cellular differentiation chromosome conformation is intricately remodelled to support the lineage-specific transcriptional programs required for initiating and maintaining lineage identity. When these changes occur in relation to cell cycle, division and time in response to cellular activatio...

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Autores principales: Chan, Wing Fuk, Coughlan, Hannah D., Zhou, Jie H. S., Keenan, Christine R., Bediaga, Naiara G., Hodgkin, Philip D., Smyth, Gordon K., Johanson, Timothy M., Allan, Rhys S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910489/
https://www.ncbi.nlm.nih.gov/pubmed/33637722
http://dx.doi.org/10.1038/s41467-021-21536-2
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author Chan, Wing Fuk
Coughlan, Hannah D.
Zhou, Jie H. S.
Keenan, Christine R.
Bediaga, Naiara G.
Hodgkin, Philip D.
Smyth, Gordon K.
Johanson, Timothy M.
Allan, Rhys S.
author_facet Chan, Wing Fuk
Coughlan, Hannah D.
Zhou, Jie H. S.
Keenan, Christine R.
Bediaga, Naiara G.
Hodgkin, Philip D.
Smyth, Gordon K.
Johanson, Timothy M.
Allan, Rhys S.
author_sort Chan, Wing Fuk
collection PubMed
description During cellular differentiation chromosome conformation is intricately remodelled to support the lineage-specific transcriptional programs required for initiating and maintaining lineage identity. When these changes occur in relation to cell cycle, division and time in response to cellular activation and differentiation signals has yet to be explored, although it has been proposed to occur during DNA synthesis or after mitosis. Here, we elucidate the chromosome conformational changes in B lymphocytes as they differentiate and expand from a naive, quiescent state into antibody secreting plasma cells. We find gene-regulatory chromosome reorganization in late G1 phase before the first division, and that this configuration is remarkably stable as the cells massively and rapidly clonally expand. A second wave of conformational change occurs as cells terminally differentiate into plasma cells, coincident with increased time in G1 phase. These results provide further explanation for how lymphocyte fate is imprinted prior to the first division. They also suggest that chromosome reconfiguration occurs prior to DNA replication and mitosis, and is linked to a gene expression program that controls the differentiation process required for the generation of immunity.
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spelling pubmed-79104892021-03-04 Pre-mitotic genome re-organisation bookends the B cell differentiation process Chan, Wing Fuk Coughlan, Hannah D. Zhou, Jie H. S. Keenan, Christine R. Bediaga, Naiara G. Hodgkin, Philip D. Smyth, Gordon K. Johanson, Timothy M. Allan, Rhys S. Nat Commun Article During cellular differentiation chromosome conformation is intricately remodelled to support the lineage-specific transcriptional programs required for initiating and maintaining lineage identity. When these changes occur in relation to cell cycle, division and time in response to cellular activation and differentiation signals has yet to be explored, although it has been proposed to occur during DNA synthesis or after mitosis. Here, we elucidate the chromosome conformational changes in B lymphocytes as they differentiate and expand from a naive, quiescent state into antibody secreting plasma cells. We find gene-regulatory chromosome reorganization in late G1 phase before the first division, and that this configuration is remarkably stable as the cells massively and rapidly clonally expand. A second wave of conformational change occurs as cells terminally differentiate into plasma cells, coincident with increased time in G1 phase. These results provide further explanation for how lymphocyte fate is imprinted prior to the first division. They also suggest that chromosome reconfiguration occurs prior to DNA replication and mitosis, and is linked to a gene expression program that controls the differentiation process required for the generation of immunity. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910489/ /pubmed/33637722 http://dx.doi.org/10.1038/s41467-021-21536-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chan, Wing Fuk
Coughlan, Hannah D.
Zhou, Jie H. S.
Keenan, Christine R.
Bediaga, Naiara G.
Hodgkin, Philip D.
Smyth, Gordon K.
Johanson, Timothy M.
Allan, Rhys S.
Pre-mitotic genome re-organisation bookends the B cell differentiation process
title Pre-mitotic genome re-organisation bookends the B cell differentiation process
title_full Pre-mitotic genome re-organisation bookends the B cell differentiation process
title_fullStr Pre-mitotic genome re-organisation bookends the B cell differentiation process
title_full_unstemmed Pre-mitotic genome re-organisation bookends the B cell differentiation process
title_short Pre-mitotic genome re-organisation bookends the B cell differentiation process
title_sort pre-mitotic genome re-organisation bookends the b cell differentiation process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910489/
https://www.ncbi.nlm.nih.gov/pubmed/33637722
http://dx.doi.org/10.1038/s41467-021-21536-2
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