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The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells

High mobility group box 1 (HMGB1) is an abundant non-histone nuclear protein that functions as a structural protein of chromatin, regulating genome replication and recombination, mRNA transcription and DNA repair. HMGB1 has been implicated in the tumorigenesis of various cancer types, and the upregu...

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Autores principales: Jia, Liyun, Song, Huiling, Fan, Wange, Song, Yanan, Wang, Gang, Li, Xueli, He, Ying, Yao, Anhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924194/
https://www.ncbi.nlm.nih.gov/pubmed/31897190
http://dx.doi.org/10.3892/ol.2019.11170
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author Jia, Liyun
Song, Huiling
Fan, Wange
Song, Yanan
Wang, Gang
Li, Xueli
He, Ying
Yao, Anhui
author_facet Jia, Liyun
Song, Huiling
Fan, Wange
Song, Yanan
Wang, Gang
Li, Xueli
He, Ying
Yao, Anhui
author_sort Jia, Liyun
collection PubMed
description High mobility group box 1 (HMGB1) is an abundant non-histone nuclear protein that functions as a structural protein of chromatin, regulating genome replication and recombination, mRNA transcription and DNA repair. HMGB1 has been implicated in the tumorigenesis of various cancer types, and the upregulation of HMGB1 has been demonstrated in glioma cells. However, the association between HMGB1 and the mitotic chromosomes in glioma remains uncharacterized. In the present study, the sub-cellular localization of HMGB1 in glioma tissues and cells was investigated. In addition, enhanced green fluorescent protein (EGFP)-tagging of the human HMGB1 protein and chromosome spreading were used to investigate the combination of HMGB1 with mitotic chromosomes. The results of the current study indicated that HMGB1 was localized to the nucleus and the cytoplasm, and it was determined to combine with the condensed chromosomes of proliferating cells in paraformaldehyde (PFA)-fixed glioma tissues. However, HMGB1 was also associated with interphase (but not mitotic chromosomes) when fixed with chilled methanol and 5% (v/v) acetic acid or PFA in vitro. Data from live cell imaging and chromosome spreading indicated the association of HMGB1 with mitotic chromosomes in glioma cells. The present results suggest that HMGB1 combines with mitotic chromosomes in glioma cells, and that the use of fixatives may result in the dissociation of the HMGB1-DNA interaction. Therefore, in live specimens and chromosome spreads, EGFP fusion proteins may represent an accurate indicator for the determination of the correct localization and interaction of HMGB1 in glioma cells.
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spelling pubmed-69241942020-01-02 The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells Jia, Liyun Song, Huiling Fan, Wange Song, Yanan Wang, Gang Li, Xueli He, Ying Yao, Anhui Oncol Lett Articles High mobility group box 1 (HMGB1) is an abundant non-histone nuclear protein that functions as a structural protein of chromatin, regulating genome replication and recombination, mRNA transcription and DNA repair. HMGB1 has been implicated in the tumorigenesis of various cancer types, and the upregulation of HMGB1 has been demonstrated in glioma cells. However, the association between HMGB1 and the mitotic chromosomes in glioma remains uncharacterized. In the present study, the sub-cellular localization of HMGB1 in glioma tissues and cells was investigated. In addition, enhanced green fluorescent protein (EGFP)-tagging of the human HMGB1 protein and chromosome spreading were used to investigate the combination of HMGB1 with mitotic chromosomes. The results of the current study indicated that HMGB1 was localized to the nucleus and the cytoplasm, and it was determined to combine with the condensed chromosomes of proliferating cells in paraformaldehyde (PFA)-fixed glioma tissues. However, HMGB1 was also associated with interphase (but not mitotic chromosomes) when fixed with chilled methanol and 5% (v/v) acetic acid or PFA in vitro. Data from live cell imaging and chromosome spreading indicated the association of HMGB1 with mitotic chromosomes in glioma cells. The present results suggest that HMGB1 combines with mitotic chromosomes in glioma cells, and that the use of fixatives may result in the dissociation of the HMGB1-DNA interaction. Therefore, in live specimens and chromosome spreads, EGFP fusion proteins may represent an accurate indicator for the determination of the correct localization and interaction of HMGB1 in glioma cells. D.A. Spandidos 2020-01 2019-12-02 /pmc/articles/PMC6924194/ /pubmed/31897190 http://dx.doi.org/10.3892/ol.2019.11170 Text en Copyright: © Jia et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Jia, Liyun
Song, Huiling
Fan, Wange
Song, Yanan
Wang, Gang
Li, Xueli
He, Ying
Yao, Anhui
The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title_full The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title_fullStr The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title_full_unstemmed The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title_short The association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
title_sort association between high mobility group box 1 chromatin protein and mitotic chromosomes in glioma cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6924194/
https://www.ncbi.nlm.nih.gov/pubmed/31897190
http://dx.doi.org/10.3892/ol.2019.11170
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