Structure of an Unprecedented G-Quadruplex Scaffold in the Human c-kit Promoter
Citations Over TimeTop 1% of 2007 papers
Abstract
The c-kit oncogene is an important target in the treatment of gastrointestinal tumors. A potential approach to inhibition of the expression of this gene involves selective stabilization of G-quadruplex structures that may be induced to form in the c-kit promoter region. Here we report on the structure of an unprecedented intramolecular G-quadruplex formed by a G-rich sequence in the c-kit promoter in K+ solution. The structure represents a new folding topology with several unique features. Most strikingly, an isolated guanine is involved in G-tetrad core formation, despite the presence of four three-guanine tracts. There are four loops: two single-residue double-chain-reversal loops, a two-residue loop, and a five-residue stem-loop, which contain base-pairing alignments. This unique structural scaffold provides a highly specific platform for the future design of ligands specifically targeted to the promoter DNA of c-kit.
Related Papers
- → Small-molecule interaction with a five-guanine-tract G-quadruplex structure from the human MYC promoter(2005)507 cited
- → Effects of Site-Specific Guanine C8-Modifications on an Intramolecular DNA G-Quadruplex(2011)53 cited
- → Label-free fluorescent and electrochemical biosensors based on defective G-quadruplexes(2018)19 cited
- → Going Platinum to the Tune of a Remarkable Guanine Quadruplex Binder: Solution‐ and Solid‐State Investigations.(2020)18 cited
- → Going Platinum to the Tune of a Remarkable Guanine Quadruplex Binder: Solution‐ and Solid‐State Investigations.(2020)1 cited