Abstract

The c-MYC oncogene mediates multiple tumor cell survival pathways and is dysregulated or overexpressed in the majority of human cancers. The NHE III1 region of the c-MYC promoter forms a DNA quadruplex. Stabilization of this structure with small molecules has been shown to reduce expression of c-MYC, and targeting the c-MYC quadruplex has become an emerging strategy for development of antitumor compounds. Previous solution NMR studies of the c-MYC quadruplex have assigned the major conformer and topology of this important target, however, regions outside the G-quartet core were not as well-defined. Here, we report a high-resolution crystal structure (2.35 Å) of the major quadruplex formed in the NHE III1 region of the c-MYC promoter. The crystal structure is in general agreement with the solution NMR structure, however, key differences are observed in the position of nucleotides outside the G-quartet core. The crystal structure provides an alternative model that, along with comparisons to other reported quadruplex crystal structures, will be important to the rational design of selective compounds. This work will aid in development of ligands to target the c-MYC promoter quadruplex with the goal of creating novel anticancer therapies.

Highlights

  • Guanine-rich sequences of DNA and RNA can form a secondary nucleic acid structure known as a quadruplex

  • In the reported complex structure, it is suggested quadruplex destabilization by the helicase results in a one-residue shift of the nucleotides involved in formation of the three G-quartets, causing the quartet nearest to the 5’-head region to be reformed by G4, G8, A12, and T16. This finding is noteworthy, due to the low-resolution of the structure and rearrangement. In this manuscript we report a high-resolution crystal structure of the major quadruplex formed in the promoter region of the human c-MYC oncogene

  • The more exposed G-quartets observed in the crystal structure, in comparison to those reported using solution NMR, confirm both the flexibility of the head and tail regions of the promoter sequence and the rigid nature of the G-quartets in this quadruplex

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Summary

Introduction

Guanine-rich sequences of DNA and RNA can form a secondary nucleic acid structure known as a quadruplex. Quadruplex motifs have become the subject of significant interest due to their presence in human telomeres, 5’-untranstranslated regions of mRNA, and in gene promoter regions [1]. One such quadruplex-forming sequence is found in the promoter region of the human c-MYC oncogene. Stabilization of the major quadruplex formed in the c-MYC promoter by various small molecules has been shown to inhibit transcription of c-MYC thereby reducing expression of the oncogene [3,4]

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