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.

Nucleic Acids Research
|December 15, 2018
PubMed

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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