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Insights into telomeric G-quadruplex DNA recognition by HMGB1 protein
- Source :
- Nucleic Acids Research, PubMed Central, UnpayWall, ORCID, Microsoft Academic Graph, Datacite
- Publication Year :
- 2019
- Publisher :
- Oxford University Press (OUP), 2019.
-
Abstract
- 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.
- Subjects :
- Cell biology
DNA repair
DNA damage
chemical and pharmacologic phenomena
Biology
G-quadruplex
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Structural Biology
Transcription (biology)
Escherichia coli
Genetics
Humans
Gene silencing
HMGB1 Protein
Telomerase
030304 developmental biology
0303 health sciences
DNA
Telomere
G-Quadruplexes
chemistry
Nucleic acid
030220 oncology & carcinogenesis
Magnetic Resonance Spectroscopy, Protein, K+ SOLUTION, BINDING, DOMAIN, CELLS, BOXES, D(TTAGGGT)(4), POLYMORPHISM, EXTENSION, COMPLEX
Nucleic Acid Conformation
Subjects
Details
- ISSN :
- 13624962 and 03051048
- Volume :
- 47
- Database :
- OpenAIRE
- Journal :
- Nucleic Acids Research
- Accession number :
- edsair.doi.dedup.....8b7b20352b9d84185820fb7be067a723
- Full Text :
- https://doi.org/10.1093/nar/gkz727