Triplex-forming oligonucleotides as modulators of gene expression

被引:72
作者
Guntaka, RV
Varma, BR
Weber, KT
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Mol Sci, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Med, Memphis, TN 38163 USA
关键词
triplex formation; stability; transcription; antigene; G-quartet;
D O I
10.1016/S1357-2725(02)00165-6
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
Triplex-forming oligonucleotides (TFOs) have gained prominence in the recent years because of their potential applications in antigene therapy. In particular they have been used as (i) inducers of site-specific mutations, (ii) reagents that selectively and specifically cleave target DNA, and (iii) as modulators of gene expression. In this mini-review, we have made an attempt to highlight the characteristics of these TFOs and the effects of various modifications in the phosphate backbone as well as in the purine and pyrimidine moieties, which contribute to the stability and efficiency of triplex formation. Studies to explore the mechanism of down-regulation of transcription of various genes suggest that at least some TFOs exert their effect by inhibiting binding of specific transcription factors to their cognate cis-acting elements. Recent reports indicate the presence of these potential triplex-forming DNA structures in the genomes of prokaryotes and eukaryotes that may play a major role in target site selection and chromosome segregation as well as in the cause of heritable diseases. Finally, some potential problems in the development of these TFOs as antigene therapeutic agents have also been discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:22 / 31
页数:10
相关论文
共 99 条
[1]   Importance of nucleotide sequence and chemical modifications of antisense oligonucleotides [J].
Agrawal, S .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1489 (01) :53-68
[2]   Design and optimization of camptothecin conjugates of triple helix-forming oligonucleotides for sequence-specific DNA cleavage by topoisomerase [J].
Arimondo, PB ;
Boutorine, A ;
Baldeyrou, B ;
Bailly, C ;
Kuwahara, M ;
Hecht, SM ;
Sun, JS ;
Garestier, T ;
Hélène, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3132-3140
[3]   Triple helix-forming oligonucleotides conjugated to indolocarbazole poisons direct topoisomerase I-mediated DNA cleavage to a specific site [J].
Arimondo, PB ;
Bailly, C ;
Boutorine, AS ;
Moreau, P ;
Prudhomme, M ;
Sun, JS ;
Garestier, T ;
Hélène, C .
BIOCONJUGATE CHEMISTRY, 2001, 12 (04) :501-509
[4]   Recognition and cleavage of DNA by rebeccamycin- or benzopyridoquinoxaline conjugated of triple helix-forming oligonucleotides [J].
Arimondo, PB ;
Moreau, P ;
Boutorine, A ;
Bailly, C ;
Prudhomme, M ;
Sun, JS ;
Garestier, T ;
Hélène, C .
BIOORGANIC & MEDICINAL CHEMISTRY, 2000, 8 (04) :777-784
[5]   Synthesis and properties of triple helix-forming oligodeoxyribonucleotides containing 7-chloro-7-deaza-2′-deoxyguanosine [J].
Aubert, Y ;
Perrouault, L ;
Hélène, C ;
Giovannangeli, C ;
Asseline, U .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (06) :1617-1624
[6]   Understanding oligonucleotide-mediated inhibition of gene expression in Xenopus laevis oocytes [J].
Bailey, C ;
Weeks, DL .
NUCLEIC ACIDS RESEARCH, 2000, 28 (05) :1154-1161
[7]   Unambiguous demonstration of triple-helix-directed gene modification [J].
Barre, FX ;
Ait-Si-Ali, S ;
Giovannangeli, C ;
Luis, R ;
Robin, P ;
Pritchard, LL ;
Hélène, C ;
Harel-Bellan, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3084-3088
[8]   Triplex formation by morpholino oligodeoxyribonucleotides in the HER-2/neu promoter requires the pyrimidine motif [J].
Basye, J ;
Trent, JO ;
Gao, DQ ;
Ebbinghaus, SW .
NUCLEIC ACIDS RESEARCH, 2001, 29 (23) :4873-4880
[9]   Antiproliferative activity of G-rich oligonucleotides correlates with protein binding [J].
Bates, PJ ;
Kahlon, JB ;
Thomas, SD ;
Trent, JO ;
Miller, DM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26369-26377
[10]   Stimulation of RecA-mediated D-loop formation by oligonucleotide-directed triple-helix formation: Guided homologous recombination (GOREC) [J].
Biet, E ;
Maurisse, R ;
Dutreix, M ;
Sun, JS .
BIOCHEMISTRY, 2001, 40 (06) :1779-1786