Four-stranded DNA: cancer, gene regulation and drug development

被引:62
作者
Huppert, Julian Leon [1 ]
机构
[1] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2007年 / 365卷 / 1861期
关键词
G-quadruplex; DNA; gene; ligand; four-stranded; regulation;
D O I
10.1098/rsta.2007.0011
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA can form many structures other than the famous double helix. In particular, guanine-rich DNA of particular sequences can form four-stranded structures, called G-quadruplexes. This article describes the structural form of these sequences, techniques for predicting which sequences can fold up in this manner and efforts towards stability prediction. It then discusses the biological significance of these structures, focusing on their importance in telomeric regions at the end of chromosomes, and their existence in gene promoters and mRNA, where they may be involved with regulating transcription and translation, respectively. Ligands that are capable of selectively binding to these structures are introduced and described, as are DNA aptamers that form G-quadruplex structures; both of these classes of compound have been investigated as anticancer agents in clinical trials. The growing use of G-quadruplexes in the nanotechnology field is also outlined. The article concludes with an analysis of future directions the field may take, with some proposals for further important studies.
引用
收藏
页码:2969 / 2984
页数:16
相关论文
共 66 条
  • [1] Solution structure of the biologically relevant g-quadruplex element in the human c-MYC promoter. implications for g-quadruplex stabilization
    Ambrus, A
    Chen, D
    Dai, JX
    Jones, RA
    Yang, DZ
    [J]. BIOCHEMISTRY, 2005, 44 (06) : 2048 - 2058
  • [2] Balasubramanian S, 2006, RSC BIOMOL SCI, pV
  • [3] Bang I, 1910, BIOCHEM Z, V26, P293
  • [4] Antiproliferative activity of G-rich oligonucleotides correlates with protein binding
    Bates, PJ
    Kahlon, JB
    Thomas, SD
    Trent, JO
    Miller, DM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) : 26369 - 26377
  • [5] STRUCTURE AND FUNCTION OF TELOMERES
    BLACKBURN, EH
    [J]. NATURE, 1991, 350 (6319) : 569 - 573
  • [6] SELECTION OF SINGLE-STRANDED-DNA MOLECULES THAT BIND AND INHIBIT HUMAN THROMBIN
    BOCK, LC
    GRIFFIN, LC
    LATHAM, JA
    VERMAAS, EH
    TOOLE, JJ
    [J]. NATURE, 1992, 355 (6360) : 564 - 566
  • [7] Cech TR, 2000, ANGEW CHEM INT EDIT, V39, P34, DOI 10.1002/(SICI)1521-3773(20000103)39:1<34::AID-ANIE34>3.0.CO
  • [8] 2-N
  • [9] 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
    Cogoi, S
    Quadrifoglio, F
    Xodo, LE
    [J]. BIOCHEMISTRY, 2004, 43 (09) : 2512 - 2523
  • [10] An intramolecular G-quadruplex structure with mixed parallel/antiparallel G-strands formed in the human BCL-2 promoter region in solution
    Dai, JX
    Dexheimer, TS
    Chen, D
    Carver, M
    Ambrus, A
    Jones, RA
    Yang, DZ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (04) : 1096 - 1098