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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
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.
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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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