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DNA G-quadruplex structures: more than simple roadblocks to transcription?

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TLDR
In this article, the formation of G-quadruplex (G4) secondary structures in gene promoters was first linked to the regulation of gene expression, and a model that placed these non-canonical DNA structures as repressors of transcription by preventing polymerase processivity was proposed.
Abstract
It has been >20 years since the formation of G-quadruplex (G4) secondary structures in gene promoters was first linked to the regulation of gene expression. Since then, the development of small molecules to selectively target G4s and their cellular application have contributed to an improved understanding of how G4s regulate transcription. One model that arose from this work placed these non-canonical DNA structures as repressors of transcription by preventing polymerase processivity. Although a considerable number of studies have recently provided sufficient evidence to reconsider this simplistic model, there is still a misrepresentation of G4s as transcriptional roadblocks. In this review, we will challenge this model depicting G4s as simple 'off switches' for gene expression by articulating how their formation has the potential to alter gene expression at many different levels, acting as a key regulatory element perturbing the nature of epigenetic marks and chromatin architecture.

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Citations
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Journal ArticleDOI

Genome-wide mapping of G-quadruplex structures with CUT&Tag

TL;DR: In this paper, the authors report the use of cleavage under targets and tagmentation (CUT&Tag) for mapping native G4 in mammalian cell lines at high resolution and low background.
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G4-quadruplex-binding proteins: review and insights into selectivity

TL;DR: A recent review summarizes the current literature on G4BPs with regards to their interactions with G4Qs, providing groupings for binding mode, drawing conclusions around commonalities and highlighting information on specific interactions as discussed by the authors .
Journal ArticleDOI

Major Achievements in the Design of Quadruplex-Interactive Small Molecules

TL;DR: The major achievements on the therapeutic potential of such quadruplex ligands, their mode of binding, effects upon interaction with quadruplexes, and the opportunities and challenges for their exploitation in drug discovery are surveyed.
Journal ArticleDOI

Folding dynamics of polymorphic G-quadruplex structures.

TL;DR: In this article, a review of recent experimental approaches to monitor G4 folding and discuss structural aspects for possible folding pathways is presented, along with comprehensive models of the complex folding energy landscape of G4s that are evaluated based on computational and experimental evidence.
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OUP accepted manuscript

TL;DR: In this article , the authors showed that APE1 (apurinic/apyrimidinic endonuclease 1), a multifunctional DNA repair enzyme, is a G-quadruplex (G4) binding protein, and loss of APE 1 abrogates the formation of stable G4 structures in cells.
References
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Journal ArticleDOI

Topological domains in mammalian genomes identified by analysis of chromatin interactions

TL;DR: It is found that the boundaries of topological domains are enriched for the insulator binding protein CTCF, housekeeping genes, transfer RNAs and short interspersed element (SINE) retrotransposons, indicating that these factors may have a role in establishing the topological domain structure of the genome.
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Regulation of chromatin by histone modifications

TL;DR: The known histone modifications are described, where they are found genomically and discussed and some of their functional consequences are discussed, concentrating mostly on transcription where the majority of characterisation has taken place.
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Chromatin structure: a repeating unit of histones and DNA.

TL;DR: Preliminary results do show less cross-linking of histones in chromatin than in solution, but crosslinked products up to pentamers are readily observed and call for further investigation.
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Direct evidence for a G-quadruplex in a promoter region and its targeting with a small molecule to repress c-MYC transcription.

TL;DR: The principle that c-MYC transcription can be controlled by ligand-mediated G-quadruplex stabilization is established, establishing the principle that the purine-rich strand of the DNA in this region can form two different intramolecular G- quadruplex structures.
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Crystal structure of parallel quadruplexes from human telomeric DNA.

TL;DR: This crystal structure of a quadruplex formed from four consecutive human telomeric DNA repeats and grown at a K+ concentration that approximates its intracellular concentration suggests a straightforward path for telomere folding and unfolding, as well as ways in which it can recognize telomerre-associated proteins.
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