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A transient ischemic environment induces reversible compaction of chromatin

BACKGROUND: Cells detect and adapt to hypoxic and nutritional stress through immediate transcriptional, translational and metabolic responses. The environmental effects of ischemia on chromatin nanostructure were investigated using single molecule localization microscopy of DNA binding dyes and of a...

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Autores principales: Kirmes, Ina, Szczurek, Aleksander, Prakash, Kirti, Charapitsa, Iryna, Heiser, Christina, Musheev, Michael, Schock, Florian, Fornalczyk, Karolina, Ma, Dongyu, Birk, Udo, Cremer, Christoph, Reid, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635527/
https://www.ncbi.nlm.nih.gov/pubmed/26541514
http://dx.doi.org/10.1186/s13059-015-0802-2
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author Kirmes, Ina
Szczurek, Aleksander
Prakash, Kirti
Charapitsa, Iryna
Heiser, Christina
Musheev, Michael
Schock, Florian
Fornalczyk, Karolina
Ma, Dongyu
Birk, Udo
Cremer, Christoph
Reid, George
author_facet Kirmes, Ina
Szczurek, Aleksander
Prakash, Kirti
Charapitsa, Iryna
Heiser, Christina
Musheev, Michael
Schock, Florian
Fornalczyk, Karolina
Ma, Dongyu
Birk, Udo
Cremer, Christoph
Reid, George
author_sort Kirmes, Ina
collection PubMed
description BACKGROUND: Cells detect and adapt to hypoxic and nutritional stress through immediate transcriptional, translational and metabolic responses. The environmental effects of ischemia on chromatin nanostructure were investigated using single molecule localization microscopy of DNA binding dyes and of acetylated histones, by the sensitivity of chromatin to digestion with DNAseI, and by fluorescence recovery after photobleaching (FRAP) of core and linker histones. RESULTS: Short-term oxygen and nutrient deprivation of the cardiomyocyte cell line HL-1 induces a previously undescribed chromatin architecture, consisting of large, chromatin-sparse voids interspersed between DNA-dense hollow helicoid structures 40–700 nm in dimension. The chromatin compaction is reversible, and upon restitution of normoxia and nutrients, chromatin transiently adopts a more open structure than in untreated cells. The compacted state of chromatin reduces transcription, while the open chromatin structure induced upon recovery provokes a transitory increase in transcription. Digestion of chromatin with DNAseI confirms that oxygen and nutrient deprivation induces compaction of chromatin. Chromatin compaction is associated with depletion of ATP and redistribution of the polyamine pool into the nucleus. FRAP demonstrates that core histones are not displaced from compacted chromatin; however, the mobility of linker histone H1 is considerably reduced, to an extent that far exceeds the difference in histone H1 mobility between heterochromatin and euchromatin. CONCLUSIONS: These studies exemplify the dynamic capacity of chromatin architecture to physically respond to environmental conditions, directly link cellular energy status to chromatin compaction and provide insight into the effect ischemia has on the nuclear architecture of cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0802-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-46355272015-11-07 A transient ischemic environment induces reversible compaction of chromatin Kirmes, Ina Szczurek, Aleksander Prakash, Kirti Charapitsa, Iryna Heiser, Christina Musheev, Michael Schock, Florian Fornalczyk, Karolina Ma, Dongyu Birk, Udo Cremer, Christoph Reid, George Genome Biol Research BACKGROUND: Cells detect and adapt to hypoxic and nutritional stress through immediate transcriptional, translational and metabolic responses. The environmental effects of ischemia on chromatin nanostructure were investigated using single molecule localization microscopy of DNA binding dyes and of acetylated histones, by the sensitivity of chromatin to digestion with DNAseI, and by fluorescence recovery after photobleaching (FRAP) of core and linker histones. RESULTS: Short-term oxygen and nutrient deprivation of the cardiomyocyte cell line HL-1 induces a previously undescribed chromatin architecture, consisting of large, chromatin-sparse voids interspersed between DNA-dense hollow helicoid structures 40–700 nm in dimension. The chromatin compaction is reversible, and upon restitution of normoxia and nutrients, chromatin transiently adopts a more open structure than in untreated cells. The compacted state of chromatin reduces transcription, while the open chromatin structure induced upon recovery provokes a transitory increase in transcription. Digestion of chromatin with DNAseI confirms that oxygen and nutrient deprivation induces compaction of chromatin. Chromatin compaction is associated with depletion of ATP and redistribution of the polyamine pool into the nucleus. FRAP demonstrates that core histones are not displaced from compacted chromatin; however, the mobility of linker histone H1 is considerably reduced, to an extent that far exceeds the difference in histone H1 mobility between heterochromatin and euchromatin. CONCLUSIONS: These studies exemplify the dynamic capacity of chromatin architecture to physically respond to environmental conditions, directly link cellular energy status to chromatin compaction and provide insight into the effect ischemia has on the nuclear architecture of cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0802-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-05 2015 /pmc/articles/PMC4635527/ /pubmed/26541514 http://dx.doi.org/10.1186/s13059-015-0802-2 Text en © Kirmes et al. 2015 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
Kirmes, Ina
Szczurek, Aleksander
Prakash, Kirti
Charapitsa, Iryna
Heiser, Christina
Musheev, Michael
Schock, Florian
Fornalczyk, Karolina
Ma, Dongyu
Birk, Udo
Cremer, Christoph
Reid, George
A transient ischemic environment induces reversible compaction of chromatin
title A transient ischemic environment induces reversible compaction of chromatin
title_full A transient ischemic environment induces reversible compaction of chromatin
title_fullStr A transient ischemic environment induces reversible compaction of chromatin
title_full_unstemmed A transient ischemic environment induces reversible compaction of chromatin
title_short A transient ischemic environment induces reversible compaction of chromatin
title_sort transient ischemic environment induces reversible compaction of chromatin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635527/
https://www.ncbi.nlm.nih.gov/pubmed/26541514
http://dx.doi.org/10.1186/s13059-015-0802-2
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