Self-organization of G-quadruplex structures in the hTERT core promoter stabilized by polyaminic side chain perylene derivatives

被引:24
作者
Micheli, Emanuela [1 ,2 ]
Martufi, Matteo [1 ]
Cacchione, Stefano [1 ]
De Santis, Pasquale [2 ]
Savino, Maria [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Biol & Biotecnol, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
关键词
G-quadruplex; Telomerase; hTERT promoter; Perylene derivatives; Induced circular dichroism (ICD); TELOMERIC G-QUADRUPLEX; DNA; SEQUENCE; LIGANDS; INHIBITION; DIIMIDES; DESIGN; SERIES; GENE;
D O I
10.1016/j.bpc.2010.10.003
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
hTERT core promoter regulates telomerase transcription in human cells, thus its structural features are of large interest. We have found that the G-rich hTERT core promoter region, corresponding to the major DNase I hypersensitive site in chromatin organization, contains nine putative G-quadruplex forming sequences (PQS) and is unfavorable for nucleosome formation. Here we show that four PQS are effectively able to form stable parallel intramolecular G-quadruplexes, using PAGE and CD spectroscopy analysis. The PQS-region, as a whole, appears to be organized in three self-interacting G-quadruplexes, probably giving rise to a helicoidal superstructure, as shown by CD and polymerase stop assay. POL-HPDI drugs, that we previously found useful in selectively stabilizing telomeric G-quadruplex, are able to stabilize both the single intramolecular G-quadruplex and the PQS-region superstructure. The features of their induced CD spectra suggest that POL-HPDIs bind to single G-quadruplexes and to whole PQS-region superstructure, mainly by end-stacking interactions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 53
页数:11
相关论文
共 41 条
  • [1] From the sequence to the superstructural properties of DNAs
    Anselmi, C
    De Santis, R
    Paparcone, R
    Savino, M
    Scipioni, A
    [J]. BIOPHYSICAL CHEMISTRY, 2002, 95 (01) : 23 - 47
  • [2] Quadruplex DNA: sequence, topology and structure
    Burge, Sarah
    Parkinson, Gary N.
    Hazel, Pascale
    Todd, Alan K.
    Neidle, Stephen
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (19) : 5402 - 5415
  • [3] G-Quadruplex DNA Sequences Are Evolutionarily Conserved and Associated with Distinct Genomic Features in Saccharomyces cerevisiae
    Capra, John A.
    Paeschke, Katrin
    Singh, Mona
    Zakian, Virginia A.
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2010, 6 (07) : 9
  • [4] G-quadruplex formation within the promoter of the KRAS proto-oncogene and its effect on transcription
    Cogoi, Susanna
    Xodo, Luigi E.
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (09) : 2536 - 2549
  • [5] Telomeres and Telomerase: From Discovery to Clinical Trials
    Corey, David R.
    [J]. CHEMISTRY & BIOLOGY, 2009, 16 (12): : 1219 - 1223
  • [6] The Design of G-quadruplex Ligands as Telomerase Inhibitors
    Cuesta, Javier
    Read, Martin A.
    Neidle, Stephen
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2003, 3 (01) : 11 - 21
  • [7] Biophysical and biological properties of quadruplex oligodeoxyribonucleotides
    Dapic, V
    Abdomerovic, V
    Marrington, R
    Peberdy, J
    Rodger, A
    Trent, JO
    Bates, PJ
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (08) : 2097 - 2107
  • [8] Prediction of Nucleosome Positioning in Genomes: Limits and Perspectives of Physical and Bioinformatic Approaches
    De Santis, Pasquale
    Morosetti, Stefano
    Scipioni, Anita
    [J]. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2010, 27 (06) : 747 - 764
  • [9] Antisense oligonucleotide-mediated inhibition of hTERT, but not hTERC, induces rapid cell growth decline and apoptosis in the absence of telomere shortening in human prostate cancer cells
    Folini, M
    Brambilla, C
    Villa, R
    Gandellini, P
    Vignati, S
    Paduano, F
    Daidone, MG
    Zaffaroni, N
    [J]. EUROPEAN JOURNAL OF CANCER, 2005, 41 (04) : 624 - 634
  • [10] The number and distances of positive charges of polyamine side chains in a series of perylene diimides significantly influence their ability to induce G-quadruplex structures and inhibit human telomerase
    Franceschin, Marco.
    Lombardo, Caterina Maria
    Pascucci, Emanuela
    D'Ambrosio, Danilo
    Micheli, Emanuela
    Bianco, Armandodoriano
    Ortaggi, Giancarlo
    Savino, Maria
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (05) : 2292 - 2304