A G-Rich Sequence within the c-kit Oncogene Promoter Forms a Parallel G-Quadruplex Having Asymmetric G-Tetrad Dynamics

被引:186
作者
Hsu, Shang-Te Danny [2 ]
Varnai, Peter [4 ]
Bugaut, Anthony [2 ]
Reszka, Anthony P. [1 ]
Neidle, Stephen [1 ]
Balasubramanian, Shankar [2 ,3 ]
机构
[1] Univ London, Sch Pharm, Canc Res UK, Biomol Struct Grp, London WC1N 1AX, England
[2] Univ Cambridge, Univ Chem Lab, Cambridge CB2 1EW, England
[3] Univ Cambridge, Sch Clin Med, Cambridge CB2 0SP, England
[4] Univ Sussex, Dept Chem & Biochem, Brighton BN1 9QJ, E Sussex, England
基金
英国生物技术与生命科学研究理事会;
关键词
GASTROINTESTINAL STROMAL TUMORS; HUMAN TELOMERIC DNA; MYC PROMOTER; K+ SOLUTION; TYROSINE KINASE; SMALL-MOLECULE; HUMAN GENOME; CLINICAL-IMPLICATIONS; HYDROGEN-EXCHANGE; GENE-EXPRESSION;
D O I
10.1021/ja904007p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Guanine-rich DNA sequences with the ability to form quadruplex structures are enriched in the promoter regions of protein-coding genes, particularly those of proto-oncogenes. G-quadruplexes are structurally polymorphic and their folding topologies can depend on the sample conditions. We report here on a structural study using solution state NMR spectroscopy of a second G-quadruplex-forming motif (c-kit2) that has been recently identified in the promoter region of the c-kit oncogene. In the presence of potassium ions, c-kit2 exists as an ensemble of structures that share the same parallel-stranded propeller-type conformations. Subtle differences in structural dynamics have been identified using hydrogen-deuterium exchange experiments by NMR spectroscopy, suggesting the coexistence of at least two structurally similar but dynamically distinct substates, which undergo slow interconversion on the NMR timescale.
引用
收藏
页码:13399 / 13409
页数:11
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