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

被引:344
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
相关论文
共 41 条
[1]   Solution structure of the biologically relevant g-quadruplex element in the human c-MYC promoter. implications for g-quadruplex stabilization [J].
Ambrus, A ;
Chen, D ;
Dai, JX ;
Jones, RA ;
Yang, DZ .
BIOCHEMISTRY, 2005, 44 (06) :2048-2058
[2]   HAIRPIN AND PARALLEL QUARTET STRUCTURES FOR TELOMERIC SEQUENCES [J].
BALAGURUMOORTHY, P ;
BRAHMACHARI, SK ;
MOHANTY, D ;
BANSAL, M ;
SASISEKHARAN, V .
NUCLEIC ACIDS RESEARCH, 1992, 20 (15) :4061-4067
[3]  
Chu Tang-Yuan, 1995, Proceedings of the National Science Council Republic of China Part B Life Sciences, V19, P8
[4]   G-rich oligonucleotide inhibits the binding of a nuclear protein to the Ki-ras promoter and strongly reduces cell growth in human carcinoma pancreatic cells [J].
Cogoi, S ;
Quadrifoglio, F ;
Xodo, LE .
BIOCHEMISTRY, 2004, 43 (09) :2512-2523
[5]   Transcriptional consequences of topoisomerase inhibition [J].
Collins, I ;
Weber, A ;
Levens, D .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (24) :8437-8451
[6]   Evidence for the presence of a guanine quadruplex forming region within a polypurine tract of the hypoxia inducible factor 1α promoter [J].
De Armond, R ;
Wood, S ;
Sun, DY ;
Hurley, LH ;
Ebbinghaus, SW .
BIOCHEMISTRY, 2005, 44 (49) :16341-16350
[7]   Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA [J].
Duquette, ML ;
Handa, P ;
Vincent, JA ;
Taylor, AF ;
Maizels, N .
GENES & DEVELOPMENT, 2004, 18 (13) :1618-1629
[8]  
Feigon J, 1995, METHOD ENZYMOL, V261, P225
[9]   HELIX FORMATION BY GUANYLIC ACID [J].
GELLERT, M ;
LIPSETT, MN ;
DAVIES, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (12) :2013-&
[10]   PROMOTION OF PARALLEL DNA QUADRUPLEXES BY A YEAST TELOMERE BINDING-PROTEIN - A CIRCULAR-DICHROISM STUDY [J].
GIRALDO, R ;
SUZUKI, M ;
CHAPMAN, L ;
RHODES, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7658-7662