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Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein
HMGB1 is a ubiquitous non-histone protein, which biological effects depend on its expression and subcellular location. Inside the nucleus, HMGB1 is engaged in many DNA events such as DNA repair, transcription and telomere maintenance. HMGB1 has been reported to bind preferentially to bent DNA as wel...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765150/ https://www.ncbi.nlm.nih.gov/pubmed/31504744 http://dx.doi.org/10.1093/nar/gkz727 |
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author | Amato, Jussara Cerofolini, Linda Brancaccio, Diego Giuntini, Stefano Iaccarino, Nunzia Zizza, Pasquale Iachettini, Sara Biroccio, Annamaria Novellino, Ettore Rosato, Antonio Fragai, Marco Luchinat, Claudio Randazzo, Antonio Pagano, Bruno |
author_facet | Amato, Jussara Cerofolini, Linda Brancaccio, Diego Giuntini, Stefano Iaccarino, Nunzia Zizza, Pasquale Iachettini, Sara Biroccio, Annamaria Novellino, Ettore Rosato, Antonio Fragai, Marco Luchinat, Claudio Randazzo, Antonio Pagano, Bruno |
author_sort | Amato, Jussara |
collection | PubMed |
description | HMGB1 is a ubiquitous non-histone protein, which biological effects depend on its expression and subcellular location. Inside the nucleus, HMGB1 is engaged in many DNA events such as DNA repair, transcription and telomere maintenance. HMGB1 has been reported to bind preferentially to bent DNA as well as to noncanonical DNA structures like 4-way junctions and, more recently, to G-quadruplexes. These are four-stranded conformations of nucleic acids involved in important cellular processes, including telomere maintenance. In this frame, G-quadruplex recognition by specific proteins represents a key event to modulate physiological or pathological pathways. Herein, to get insights into the telomeric G-quadruplex DNA recognition by HMGB1, we performed detailed biophysical studies complemented with biological analyses. The obtained results provided information about the molecular determinants for the interaction and showed that the structural variability of human telomeric G-quadruplex DNA may have significant implications in HMGB1 recognition. The biological data identified HMGB1 as a telomere-associated protein in both telomerase-positive and -negative tumor cells and showed that HMGB1 gene silencing in such cells induces telomere DNA damage foci. Altogether, these findings provide a deeper understanding of telomeric G-quadruplex recognition by HMGB1 and suggest that this protein could actually represent a new target for cancer therapy. |
format | Online Article Text |
id | pubmed-6765150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-67651502019-10-02 Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein Amato, Jussara Cerofolini, Linda Brancaccio, Diego Giuntini, Stefano Iaccarino, Nunzia Zizza, Pasquale Iachettini, Sara Biroccio, Annamaria Novellino, Ettore Rosato, Antonio Fragai, Marco Luchinat, Claudio Randazzo, Antonio Pagano, Bruno Nucleic Acids Res Structural Biology HMGB1 is a ubiquitous non-histone protein, which biological effects depend on its expression and subcellular location. Inside the nucleus, HMGB1 is engaged in many DNA events such as DNA repair, transcription and telomere maintenance. HMGB1 has been reported to bind preferentially to bent DNA as well as to noncanonical DNA structures like 4-way junctions and, more recently, to G-quadruplexes. These are four-stranded conformations of nucleic acids involved in important cellular processes, including telomere maintenance. In this frame, G-quadruplex recognition by specific proteins represents a key event to modulate physiological or pathological pathways. Herein, to get insights into the telomeric G-quadruplex DNA recognition by HMGB1, we performed detailed biophysical studies complemented with biological analyses. The obtained results provided information about the molecular determinants for the interaction and showed that the structural variability of human telomeric G-quadruplex DNA may have significant implications in HMGB1 recognition. The biological data identified HMGB1 as a telomere-associated protein in both telomerase-positive and -negative tumor cells and showed that HMGB1 gene silencing in such cells induces telomere DNA damage foci. Altogether, these findings provide a deeper understanding of telomeric G-quadruplex recognition by HMGB1 and suggest that this protein could actually represent a new target for cancer therapy. Oxford University Press 2019-10-10 2019-08-26 /pmc/articles/PMC6765150/ /pubmed/31504744 http://dx.doi.org/10.1093/nar/gkz727 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Structural Biology Amato, Jussara Cerofolini, Linda Brancaccio, Diego Giuntini, Stefano Iaccarino, Nunzia Zizza, Pasquale Iachettini, Sara Biroccio, Annamaria Novellino, Ettore Rosato, Antonio Fragai, Marco Luchinat, Claudio Randazzo, Antonio Pagano, Bruno Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title | Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title_full | Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title_fullStr | Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title_full_unstemmed | Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title_short | Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein |
title_sort | insights into telomeric g-quadruplex dna recognition by hmgb1 protein |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6765150/ https://www.ncbi.nlm.nih.gov/pubmed/31504744 http://dx.doi.org/10.1093/nar/gkz727 |
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