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High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division

BACKGROUND: Genomes of eukaryotes exist as chromatin, and it is known that different chromatin states can influence gene regulation. Chromatin is not a static structure, but is known to be dynamic and vary between cells. In order to monitor the organisation of chromatin in live cells we have enginee...

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Autores principales: Dickerson, David, Gierliński, Marek, Singh, Vijender, Kitamura, Etsushi, Ball, Graeme, Tanaka, Tomoyuki U., Owen-Hughes, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016949/
https://www.ncbi.nlm.nih.gov/pubmed/27609610
http://dx.doi.org/10.1186/s12860-016-0111-y
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author Dickerson, David
Gierliński, Marek
Singh, Vijender
Kitamura, Etsushi
Ball, Graeme
Tanaka, Tomoyuki U.
Owen-Hughes, Tom
author_facet Dickerson, David
Gierliński, Marek
Singh, Vijender
Kitamura, Etsushi
Ball, Graeme
Tanaka, Tomoyuki U.
Owen-Hughes, Tom
author_sort Dickerson, David
collection PubMed
description BACKGROUND: Genomes of eukaryotes exist as chromatin, and it is known that different chromatin states can influence gene regulation. Chromatin is not a static structure, but is known to be dynamic and vary between cells. In order to monitor the organisation of chromatin in live cells we have engineered fluorescent fusion proteins which recognize specific operator sequences to tag pairs of syntenic gene loci. The separation of these loci was then tracked in three dimensions over time using fluorescence microscopy. RESULTS: We established a work flow for measuring the distance between two fluorescently tagged, syntenic gene loci with a mean measurement error of 63 nm. In general, physical separation was observed to increase with increasing genomic separations. However, the extent to which chromatin is compressed varies for different genomic regions. No correlation was observed between compaction and the distribution of chromatin markers from genomic datasets or with contacts identified using capture based approaches. Variation in spatial separation was also observed within cells over time and between cells. Differences in the conformation of individual loci can persist for minutes in individual cells. Separation of reporter loci was found to be similar in related and unrelated daughter cell pairs. CONCLUSIONS: The directly observed physical separation of reporter loci in live cells is highly dynamic both over time and from cell to cell. However, consistent differences in separation are observed over some chromosomal regions that do not correlate with factors known to influence chromatin states. We conclude that as yet unidentified parameters influence chromatin configuration. We also find that while heterogeneity in chromatin states can be maintained for minutes between cells, it is not inherited through cell division. This may contribute to cell-to-cell transcriptional heterogeneity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-016-0111-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-50169492016-09-10 High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division Dickerson, David Gierliński, Marek Singh, Vijender Kitamura, Etsushi Ball, Graeme Tanaka, Tomoyuki U. Owen-Hughes, Tom BMC Cell Biol Research BACKGROUND: Genomes of eukaryotes exist as chromatin, and it is known that different chromatin states can influence gene regulation. Chromatin is not a static structure, but is known to be dynamic and vary between cells. In order to monitor the organisation of chromatin in live cells we have engineered fluorescent fusion proteins which recognize specific operator sequences to tag pairs of syntenic gene loci. The separation of these loci was then tracked in three dimensions over time using fluorescence microscopy. RESULTS: We established a work flow for measuring the distance between two fluorescently tagged, syntenic gene loci with a mean measurement error of 63 nm. In general, physical separation was observed to increase with increasing genomic separations. However, the extent to which chromatin is compressed varies for different genomic regions. No correlation was observed between compaction and the distribution of chromatin markers from genomic datasets or with contacts identified using capture based approaches. Variation in spatial separation was also observed within cells over time and between cells. Differences in the conformation of individual loci can persist for minutes in individual cells. Separation of reporter loci was found to be similar in related and unrelated daughter cell pairs. CONCLUSIONS: The directly observed physical separation of reporter loci in live cells is highly dynamic both over time and from cell to cell. However, consistent differences in separation are observed over some chromosomal regions that do not correlate with factors known to influence chromatin states. We conclude that as yet unidentified parameters influence chromatin configuration. We also find that while heterogeneity in chromatin states can be maintained for minutes between cells, it is not inherited through cell division. This may contribute to cell-to-cell transcriptional heterogeneity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-016-0111-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-08 /pmc/articles/PMC5016949/ /pubmed/27609610 http://dx.doi.org/10.1186/s12860-016-0111-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dickerson, David
Gierliński, Marek
Singh, Vijender
Kitamura, Etsushi
Ball, Graeme
Tanaka, Tomoyuki U.
Owen-Hughes, Tom
High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title_full High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title_fullStr High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title_full_unstemmed High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title_short High resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
title_sort high resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016949/
https://www.ncbi.nlm.nih.gov/pubmed/27609610
http://dx.doi.org/10.1186/s12860-016-0111-y
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