A conserved quadruplex motif located in a transcription activation site of the human c-kit oncogene

被引:343
作者
Fernando, Himesh
Reszka, Anthony P.
Huppert, Julian
Ladame, Sylvain
Rankin, Sarah
Venkitaraman, Ashok R.
Neidle, Stephen
Balasubramanian, Shankar
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Univ London, Sch Pharm, Canc Res UK, Biomol Struct Grp, London WC1N 1AX, England
[3] Univ Cambridge, MRC, Res Ctr, Canc Cell Unit, Cambridge CB2 2XZ, England
基金
英国医学研究理事会;
关键词
D O I
10.1021/bi0601510
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The c-kit gene encodes a receptor tyrosine kinase, whose engagement by its ligand triggers signals leading to cell proliferation. c-kit activity is elevated in gastrointestinal stromal tumors (GISTs), and its therapeutic inhibition by small molecules such as imatinib is clinically validated. We identified a putative quadruplex forming 21-nucleotide sequence upstream of the c-kit transcription initiation site (c-kit21), on the G-rich strand, which occupies a site required for core promoter activity. Here, we show by nuclear magnetic resonance (NMR), circular dichroism (CD), and ultraviolet (UV) spectroscopic methods that c-kit21 forms quadruplexes under physiological conditions. Mutational analysis of c-kit21 has provided insights into its structural polymorphism. In particular, one mutated form appears to form a single quadruplex species that adopts a parallel conformation. The quadruplex-forming sequence shows a high level of sequence conservation across human, mouse, rat, and chimpanzee. The small variation in sequence between the quadruplex in human/chimpanzee as compared to the rat/mouse was examined more closely by biophysical methods. Despite a variation in the sequence and length of loop 2, the quadruplexes showed both comparable CD spectra, indicative of parallel quadruplexes, and also similar thermal-stability profiles, suggesting conservation of biophysical characteristics. Collectively, the evidence suggests that this quadruplex is a serious target for a detailed functional investigation at the cell-biology level.
引用
收藏
页码:7854 / 7860
页数:7
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