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Updated: Feb 1, 2026

Author Spotlight: Characterizing DNA G-Quadruplex by Bis-3-Chloropiperidine Based Chemical Mapping
Published on: May 12, 2023
Structure of a (3+1) hybrid G-quadruplex in the PARP1 promoter
Anjali Sengar1, J Jeya Vandana1, Vicki S Chambers2
1School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Abstract:
Poly (ADP-ribose) polymerase 1 (PARP1) has emerged as an attractive target for cancer therapy due to its key role in DNA repair processes. Inhibition of PARP1 in BRCA-mutated cancers has been observed to be clinically beneficial. Recent genome-mapping experiments have identified a non-canonical G-quadruplex-forming sequence containing bulges within the PARP1 promoter. Structural features, like bulges, provide opportunities for selective chemical targeting of the non-canonical G-quadruplex structure within the PARP1 promoter, which could serve as an alternative therapeutic approach for the regulation of PARP1 expression. Here we report the G-quadruplex structure formed by a 23-nucleotide G-rich sequence in the PARP1 promoter. Our study revealed a three-layered intramolecular (3+1) hybrid G-quadruplex scaffold, in which three strands are oriented in one direction and the fourth in the opposite direction. This structure exhibits unique structural features such as an adenine bulge and a G·G·T base triple capping structure formed between the central edgewise loop, propeller loop and 5' flanking terminal. Given the highly important role of PARP1 in DNA repair and cancer intervention, this structure presents an attractive opportunity to explore the therapeutic potential of PARP1 inhibition via G-quadruplex DNA targeting.
Insights
Researchers discovered a unique G-quadruplex structure in the Poly (ADP-ribose) polymerase 1 (PARP1) promoter. This structure offers a novel therapeutic target for regulating PARP1 expression in cancer treatment.
Area of Science:
- Molecular Biology
- Genomics
- Cancer Therapeutics
Background:
- Poly (ADP-ribose) polymerase 1 (PARP1) is crucial for DNA repair and a target in cancer therapy, especially for BRCA-mutated cancers.
- Genome mapping revealed non-canonical G-quadruplex sequences with bulges in the PARP1 promoter.
Purpose of the Study:
- To elucidate the G-quadruplex structure formed by a specific G-rich sequence in the PARP1 promoter.
- To explore the therapeutic potential of targeting this G-quadruplex structure for PARP1 regulation.
Main Methods:
- Detailed structural analysis of the G-quadruplex formed by a 23-nucleotide G-rich sequence from the PARP1 promoter.
- Characterization of unique structural features, including bulges and base triple capping structures.
Main Results:
- A three-layered intramolecular (3+1) hybrid G-quadruplex scaffold was identified.
- The structure features an adenine bulge and a G·G·T base triple capping structure involving loops and flanking terminals.
Conclusions:
- The identified G-quadruplex structure possesses unique features amenable to selective chemical targeting.
- This structure represents a promising avenue for developing novel therapeutic strategies to inhibit PARP1 expression in cancer.
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