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DNA methylation and histone post-translational modification stability in post-mortem brain tissue

BACKGROUND: Epigenetic (including DNA and histone) modifications occur in a variety of neurological disorders. If epigenetic features of brain autopsy material are to be studied, it is critical to understand the post-mortem stability of the modifications. METHODS: Pig and mouse brain tissue were for...

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Autores principales: Jarmasz, Jessica S., Stirton, Hannah, Davie, James R., Del Bigio, Marc R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330433/
https://www.ncbi.nlm.nih.gov/pubmed/30635019
http://dx.doi.org/10.1186/s13148-018-0596-7
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author Jarmasz, Jessica S.
Stirton, Hannah
Davie, James R.
Del Bigio, Marc R.
author_facet Jarmasz, Jessica S.
Stirton, Hannah
Davie, James R.
Del Bigio, Marc R.
author_sort Jarmasz, Jessica S.
collection PubMed
description BACKGROUND: Epigenetic (including DNA and histone) modifications occur in a variety of neurological disorders. If epigenetic features of brain autopsy material are to be studied, it is critical to understand the post-mortem stability of the modifications. METHODS: Pig and mouse brain tissue were formalin-fixed and paraffin-embedded, or frozen after post-mortem delays of 0, 24, 48, and 72 h. Epigenetic modifications frequently reported in the literature were studied by DNA agarose gel electrophoresis, DNA methylation enzyme-linked immunosorbent assays, Western blotting, and immunohistochemistry. We constructed a tissue microarray of human neocortex samples with devitalization or death to fixation times ranging from < 60 min to 5 days. RESULTS: In pig and mouse brain tissue, we found that DNA cytosine modifications (5mC, 5hmC, 5fC, and 5caC) were stable for ≥ 72 h post-mortem. Histone methylation was generally stable for ≥ 48 h (H3K9me2/K9me3, H3K27me2, H3K36me3) or ≥ 72 h post-mortem (H3K4me3, H3K27me3). Histone acetylation was generally less stable. The levels of H3K9ac, H3K27ac, H4K5ac, H4K12ac, and H4K16ac declined as early as ≤ 24 h post-mortem, while the levels of H3K14ac did not change at ≥ 48 h. Immunohistochemistry showed that histone acetylation loss occurred primarily in the nuclei of large neurons, while immunoreactivity in glial cell nuclei was relatively unchanged. In the human brain tissue array, immunoreactivity for DNA cytosine modifications and histone methylation was stable, while subtle changes were apparent in histone acetylation at 4 to 5 days post-mortem. CONCLUSION: We conclude that global epigenetic studies on human post-mortem brain tissue are feasible, but great caution is needed for selection of post-mortem delay matched controls if histone acetylation is of interest. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0596-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63304332019-01-16 DNA methylation and histone post-translational modification stability in post-mortem brain tissue Jarmasz, Jessica S. Stirton, Hannah Davie, James R. Del Bigio, Marc R. Clin Epigenetics Research BACKGROUND: Epigenetic (including DNA and histone) modifications occur in a variety of neurological disorders. If epigenetic features of brain autopsy material are to be studied, it is critical to understand the post-mortem stability of the modifications. METHODS: Pig and mouse brain tissue were formalin-fixed and paraffin-embedded, or frozen after post-mortem delays of 0, 24, 48, and 72 h. Epigenetic modifications frequently reported in the literature were studied by DNA agarose gel electrophoresis, DNA methylation enzyme-linked immunosorbent assays, Western blotting, and immunohistochemistry. We constructed a tissue microarray of human neocortex samples with devitalization or death to fixation times ranging from < 60 min to 5 days. RESULTS: In pig and mouse brain tissue, we found that DNA cytosine modifications (5mC, 5hmC, 5fC, and 5caC) were stable for ≥ 72 h post-mortem. Histone methylation was generally stable for ≥ 48 h (H3K9me2/K9me3, H3K27me2, H3K36me3) or ≥ 72 h post-mortem (H3K4me3, H3K27me3). Histone acetylation was generally less stable. The levels of H3K9ac, H3K27ac, H4K5ac, H4K12ac, and H4K16ac declined as early as ≤ 24 h post-mortem, while the levels of H3K14ac did not change at ≥ 48 h. Immunohistochemistry showed that histone acetylation loss occurred primarily in the nuclei of large neurons, while immunoreactivity in glial cell nuclei was relatively unchanged. In the human brain tissue array, immunoreactivity for DNA cytosine modifications and histone methylation was stable, while subtle changes were apparent in histone acetylation at 4 to 5 days post-mortem. CONCLUSION: We conclude that global epigenetic studies on human post-mortem brain tissue are feasible, but great caution is needed for selection of post-mortem delay matched controls if histone acetylation is of interest. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0596-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-11 /pmc/articles/PMC6330433/ /pubmed/30635019 http://dx.doi.org/10.1186/s13148-018-0596-7 Text en © The Author(s). 2019 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
Jarmasz, Jessica S.
Stirton, Hannah
Davie, James R.
Del Bigio, Marc R.
DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title_full DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title_fullStr DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title_full_unstemmed DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title_short DNA methylation and histone post-translational modification stability in post-mortem brain tissue
title_sort dna methylation and histone post-translational modification stability in post-mortem brain tissue
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330433/
https://www.ncbi.nlm.nih.gov/pubmed/30635019
http://dx.doi.org/10.1186/s13148-018-0596-7
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