A Small Molecule That Disrupts G-Quadruplex DNA Structure and Enhances Gene Expression

被引:125
|
作者
Waller, Zoe. A. E. [1 ]
Sewitz, Sven A. [1 ]
Hsu, Shang-Te Danny [1 ]
Balasubramanian, Shankar [1 ,2 ]
机构
[1] Univ Cambridge, Univ Chem Lab, Cambridge CB2 1EW, England
[2] Univ Cambridge, Sch Clin Med, Cambridge CB2 0SP, England
基金
英国生物技术与生命科学研究理事会;
关键词
C-KIT; PROMOTER REGION; CYTOCHROME-C; PROTOONCOGENE; POTASSIUM; BINDING; SHOW; MYC;
D O I
10.1021/ja901892u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It has been hypothesized that the formation of G-quadruplex structures in the DNA of gene promoters may be functionally linked to transcription and consequently that small. molecules that interact with such G-quadruplexes may modulate transcription. We previously reported that triarylpyridines are a class of small molecules that selectively interact with G-quadruplex DNA. Here we describe an unexpected property of one such ligand that was found to disrupt the structure of two different DNA G-quadruplex structures, each derived from sequence motifs in the promoter. of the proto-oncogene c-kit. Furthermore, cell-based experiments in a cell line that expresses c-kit (HGC-27) showed that the same ligand increased the expression of c-kit. This contrasts with G-quadruplex-inducing ligands that have been previously found to inhibit gene expression. It would thus appear that the functional consequence of small molecule ligands interacting with G-quadruplex structures may depend on the specific mode of interaction. These observations provide further evidence to suggest that G-quadruplex forming sequence motifs play a role that relates to transcription.
引用
收藏
页码:12628 / 12633
页数:6
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