Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/135050
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Type: Journal article
Title: Pre-mitotic genome re-organisation bookends the B cell differentiation process
Author: Chan, W.F.
Coughlan, H.D.
Zhou, J.H.S.
Keenan, C.R.
Bediaga, N.G.
Hodgkin, P.D.
Smyth, G.K.
Johanson, T.M.
Allan, R.S.
Citation: Nature Communications, 2021; 12(1):1344-1-1344-13
Publisher: Springer Nature
Issue Date: 2021
ISSN: 2041-1723
2041-1723
Statement of
Responsibility: 
Wing Fuk Chan, Hannah D. Coughlan, Jie H. S. Zhou, Christine R. Keenan, Naiara G. Bediaga, Philip D. Hodgkin, Gordon K. Smyth, Timothy M. Johanson, Rhys S. Allan
Abstract: 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.
Keywords: Anti-body Producing Cells
Rights: © 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/.
DOI: 10.1038/s41467-021-21536-2
Grant ID: http://purl.org/au-research/grants/nhmrc/1058892
http://purl.org/au-research/grants/nhmrc/1054925
http://purl.org/au-research/grants/nhmrc/1124081
http://purl.org/au-research/grants/nhmrc/1125436
http://purl.org/au-research/grants/nhmrc/1158531
Published version: http://dx.doi.org/10.1038/s41467-021-21536-2
Appears in Collections:Medicine publications

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