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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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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. |
format | Online Article Text |
id | pubmed-4635527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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